Analytical Chromatography

Famprofazone may be used as an analytical reference standard for the quantification of the analyte in biological samples using liquid chromatography coupled to tandem mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

10 g in poly bottle

grade	analytical standard
Quality Level	200
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	CC(C)C1=C(CN(C)C(C)Cc2ccccc2)N(C)N(c3ccccc3)C1=O
InChI	1S/C24H31N3O/c1-18(2)23-22(17-25(4)19(3)16-20-12-8-6-9-13-20)26(5)27(24(23)28)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3
InChI key	GNUXVOXXWGNPIV-UHFFFAOYSA-N

pictograms	GHS07
signalword	Warning
hcodes	H302
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Fast Green FCF is a synthetic organic dye, which belongs to the triphenylmethane group. It can be found in a wide range of applications in food and beverage industry. It can also be used in scientific research for the staining of proteins and identification of extracellular recording or injection sites in electrophysiological experiments.

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Fast Green FCF

Empirical Formula (Hill Notation):	C₃₇H₃₄N₂Na₂O₁₀S₃
Linear Formula:	C₃₇H₃₄N₂O₁₀S₃Na₂
CAS Number:	2353-45-9
Molecular Weight:	808.85
Colour Index Number:	42053
Beilstein/REAXYS Number:	5718212
EC Number:	219-091-5
MDL number:	MFCD00013053
PubChem Substance ID:	329761116
E Number:	E143
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fast Green FCF dye is used for protein staining in IEF, native PAGE and SDS-PAGE. Fast Green staining is linear over a wider range of protein concentrations than Brilliant Blue R. After electrophoresis, fixing the proteins in the gel is recommended for maximum sensitivity. The gel can then be stained for 2 hr with 0.1% Fast Green FCF in either 30% (v/v) ethanol, 10% (v/v) acetic acid or in 7% acetic acid. The gel can be destained with either 30% (v/v) ethanol, 10% (v/v) acetic acid, or 7% acetic acid. The stained gel can be scanned at 625 nm. The detection sensitivity is approx. 30% that with Brilliant Blue R.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	98.0% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	290 °C (dec.) (lit.)
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	[Na+].[Na+].CCN(Cc1cccc(c1)S([O-])(=O)=O)c2ccc(cc2)C(=C3/C=CC(\C=C3)=[N+](\CC)Cc4cccc(c4)S([O-])(=O)=O)\c5ccc(O)cc5S([O-])(=O)=O
InChI	1S/C37H36N2O10S3.2Na/c1-3-38(24-26-7-5-9-33(21-26)50(41,42)43)30-15-11-28(12-16-30)37(35-20-19-32(40)23-36(35)52(47,48)49)29-13-17-31(18-14-29)39(4-2)25-27-8-6-10-34(22-27)51(44,45)46;;/h5-23H,3-4,24-25H2,1-2H3,(H3,41,42,43,44,45,46,47,48,49);;/q;2*+1/p-2
InChI key	RZSYLLSAWYUBPE-UHFFFAOYSA-L

pictograms	GHS08
signalword	Warning
hcodes	H341
pcodes	P281
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

Fast Yellow AB (E-105) is used for the quality control in food products. It belongs to the class of water-soluble food color additives. These synthetic food colors are commonly used for the maintenance and improvement of color appearance in foods. Fast Yellow AB is one of the most recalcitrant of the azo dyes due to the arrangement of withdrawing substituents.

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Fast Yellow AB

Linear Formula:	C₁₂H₁₁N₃O₆S₂xNA
CAS Number:	79873-36-2
E Number:	E105
NACRES:	NA.24

Fast Yellow AB may be used as an analytical reference standard for the quantification of the analyte in:

Drinks and candies using reversed-phase high-performance liquid chromatography with photodiode array detection.
Commercial products such as sports drinks and bakery ink formulations using high-performance thin layer chromatography.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	97.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

Fenbendazole is a thio substituted benzimidazole, which belongs to the group of anthelmintics. It can be widely used in veterinary medicine particularly, in the treatment of helminth infections.
Chemical structure: benzimidazole

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Fenbendazole

Empirical Formula (Hill Notation):	C₁₅H₁₃N₃O₂S
CAS Number:	43210-67-9
Molecular Weight:	299.35
Beilstein/REAXYS Number:	759077
EC Number:	256-145-7
MDL number:	MFCD00144301
PubChem Substance ID:	329755115
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	COC(=O)Nc1nc2cc(Sc3ccccc3)ccc2[nH]1
InChI	1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChI key	HDDSHPAODJUKPD-UHFFFAOYSA-N

pictograms	GHS08,GHS09
signalword	Warning
hcodes	H361fd - H373 - H410
pcodes	P201 - P202 - P260 - P273 - P280 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Chemical structure: benzimidazole

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Fenbendazole sulfone

Empirical Formula (Hill Notation):	C₁₅H₁₃N₃O₄S
CAS Number:	54029-20-8
Molecular Weight:	331.35
Beilstein/REAXYS Number:	703211
MDL number:	MFCD00797921
PubChem Substance ID:	329754020
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	COC(=O)Nc1nc2cc(ccc2[nH]1)S(=O)(=O)c3ccccc3
InChI	1S/C15H13N3O4S/c1-22-15(19)18-14-16-12-8-7-11(9-13(12)17-14)23(20,21)10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)
InChI key	UAFDGCOOJPIAHN-UHFFFAOYSA-N

pictograms	GHS07,GHS09,GHS07,GHS09
signalword	Warning-Warning
hcodes	H302 - H315 - H317 - H410 - H302 - H315 - H317 - H410
pcodes	P261 - P264 - P273 - P280 - P261 - P264 - P273 - P280 - P301 + P312 - P302 + P352 - P301 + P312 - P302 + P352
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Chemical structure: benzimidazole

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Fenbendazole-d3

Empirical Formula (Hill Notation):	C₁₅D₃H₁₀N₃O₂S
CAS Number:	1228182-47-5
Molecular Weight:	302.37
MDL number:	MFCD16652570
PubChem Substance ID:	329754031
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
mass shift	M+3
SMILES string	[2H]C([2H])([2H])OC(=O)Nc1nc2cc(Sc3ccccc3)ccc2[nH]1
InChI	1S/C15H13N3O2S/c1-20-15(19)18-14-16-12-8-7-11(9-13(12)17-14)21-10-5-3-2-4-6-10/h2-9H,1H3,(H2,16,17,18,19)/i1D3
InChI key	HDDSHPAODJUKPD-FIBGUPNXSA-N

pictograms	GHS08,GHS09
signalword	Warning
hcodes	H361fd - H373 - H410
pcodes	P201 - P202 - P260 - P273 - P280 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Fenbufen belongs to the class of non-steroidal anti-inflammatory drugs, widely used as an antipyretic and analgesic in medical applications. Its mode of action involves the inhibition of cyclooxygenase enzyme and thereby prevents the synthesis of certain prostaglandins.

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Fenbufen

Empirical Formula (Hill Notation):	C₁₆H₁₄O₃
Linear Formula:	C₆H₅C₆H₄CO(CH₂)₂CO₂H
CAS Number:	36330-85-5
Molecular Weight:	254.28
EC Number:	252-979-0
MDL number:	MFCD00056701
PubChem Substance ID:	329799772
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fenbufen may be used as an analytical reference standard for the quantification of the analyte in biological samples and pharmaceutical formulations using chromatography techniques.

5, 10 g in glass bottle

grade	analytical standard
Quality Level	100
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	184-187 °C (lit.)
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	OC(=O)CCC(=O)c1ccc(cc1)-c2ccccc2
InChI	1S/C16H14O3/c17-15(10-11-16(18)19)14-8-6-13(7-9-14)12-4-2-1-3-5-12/h1-9H,10-11H2,(H,18,19)
InChI key	ZPAKPRAICRBAOD-UHFFFAOYSA-N
Gene Information	human ... MMP2(4313), MMP3(4314), MMP9(4318)

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P301 + P310
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Fenofibrate is a third-generation fibric acid derivative which is widely employed for the treatment of atherogenic dyslipidemia, hypertriglyceridemia, mixed dyslipidemia and hypercholesterolemia.

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Fenofibrate

Empirical Formula (Hill Notation):	C₂₀H₂₁ClO₄
CAS Number:	49562-28-9
Molecular Weight:	360.83
EC Number:	256-376-3
MDL number:	MFCD00133314
PubChem Substance ID:	329823250
NACRES:	NA.24

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Fenofibrate may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by various chromatography and spectrophotometry techniques.

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAC0257 in the slot below. This is an example certificate only and may not be the lot that you receive.

Quality Level	300
grade	certified reference material, pharmaceutical secondary standard
form	neat
CofA	current certificate can be downloaded
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to PhEur F0048000, traceable to USP 1269447
SMILES string	CC(C)OC(=O)C(C)(C)Oc1ccc(cc1)C(=O)c2ccc(Cl)cc2
InChI	1S/C20H21ClO4/c1-13(2)24-19(23)20(3,4)25-17-11-7-15(8-12-17)18(22)14-5-9-16(21)10-6-14/h5-13H,1-4H3
InChI key	YMTINGFKWWXKFG-UHFFFAOYSA-N
Gene Information	human ... PPARA(5465)

hcodes	H412
pcodes	P273 - P501
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

Fenofibric acid may be used as a reference standard in the determination of fenofibric acid in samples of human plasma using high performance liquid chromatography (HPLC) and liquid chromatography coupled with tandem mass spectrometry (LC-MS-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Подробнее

Fenofibric acid

Empirical Formula (Hill Notation):	C₁₇H₁₅ClO₄
CAS Number:	42017-89-0
Molecular Weight:	318.75
Beilstein/REAXYS Number:	2058973
EC Number:	255-626-9
MDL number:	MFCD00792461
PubChem Substance ID:	329769927
NACRES:	NA.24

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	1.0% water
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	O=C(C1=CC=C(OC(C)(C)C(O)=O)C=C1)C2=CC=C(Cl)C=C2
InChI	1S/C17H15ClO4/c1-17(2,16(20)21)22-14-9-5-12(6-10-14)15(19)11-3-7-13(18)8-4-11/h3-10H,1-2H3,(H,20,21)
InChI key	MQOBSOSZFYZQOK-UHFFFAOYSA-N
Gene Information	human ... PPARA(5465)

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H302 - H410
pcodes	P264 - P270 - P273 - P301 + P312 - P391 - P501
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3

Fenoprofen calcium salt hydrate may be used as an analytical reference standard for the quantification of the analyte in environmental samples using gas chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Fenoprofen calcium salt hydrate

Empirical Formula (Hill Notation):	C₃₀H₂₆CaO₆
Linear Formula:	C₃₀H₂₆O₆Ca
CAS Number:	53746-45-5
Molecular Weight:	522.60
EC Number:	252-107-9
MDL number:	MFCD00242722
PubChem Substance ID:	329799683
NACRES:	NA.24

5, 10 g in glass bottle

Quality Level	100
grade	analytical standard, for drug analysis
assay	97% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	O.[Ca].CC(C(O)=O)c1cccc(Oc2ccccc2)c1
InChI	1S/C15H14O3.Ca.H2O.2H/c1-11(15(16)17)12-6-5-9-14(10-12)18-13-7-3-2-4-8-13;;;;/h2-11H,1H3,(H,16,17);;1H2;;
InChI key	JWCQUXFJNIIYQZ-UHFFFAOYSA-N

pictograms	GHS07
signalword	Warning
hcodes	H302 + H312 + H332
pcodes	P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Finasteride may be used as an analytical reference standard for the determination of the analyte in biological fluids and pharmaceutical formulations by high performance liquid chromatography (HPLC) method.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Подробнее

Finasteride

Empirical Formula (Hill Notation):	C₂₃H₃₆N₂O₂
CAS Number:	98319-26-7
Molecular Weight:	372.54
MDL number:	MFCD00869737
PubChem Substance ID:	329754889

Selective 5α-reductase inhibitor; antiandrogen.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
SMILES string	[H][C@@]12CC[C@@]3([H])[C@]4([H])CC[C@H](C(=O)NC(C)(C)C)[C@@]4(C)CC[C@]3([H])[C@@]1(C)C=CC(=O)N2
InChI	1S/C23H36N2O2/c1-21(2,3)25-20(27)17-8-7-15-14-6-9-18-23(5,13-11-19(26)24-18)16(14)10-12-22(15,17)4/h11,13-18H,6-10,12H2,1-5H3,(H,24,26)(H,25,27)/t14-,15-,16-,17+,18+,22-,23+/m0/s1
InChI key	DBEPLOCGEIEOCV-WSBQPABSSA-N
Gene Information	human ... SRD5A2(6716)

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H360FD
pcodes	P201 - P202 - P264 - P270 - P301 + P312 - P308 + P313
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Fine dust (PM10-like) (PAHs) ERMCZ100-1VL

NACRES:

NA.24

Fine dust (PM10-like) (PAH′s) has been used as a reference material in the determination of polycyclic aromatic hydrocarbons in air samples using high performance liquid chromatography (HPLC).

For more information please see:
ERMCZ100

ERM is a registered trademark of European Commission

grade	certified reference material
Agency/Method	ERM^®
Торговая марка	JRC
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care Pharmaceutical (small molecule)
format	matrix material
storage temp.	2-8°C

pictograms	GHS08
signalword	Danger
hcodes	H372
pcodes	P260 - P264 - P270 - P314 - P501
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Подробнее

Fipexide hydrochloride

Empirical Formula (Hill Notation):	C₂₀H₂₁ClN₂O₄ · HCl
CAS Number:	34161-24-5
Molecular Weight:	425.31
EC Number:	251-857-4
MDL number:	MFCD00133323
PubChem Substance ID:	329799752
NACRES:	NA.24

5 g in poly bottle

grade	analytical standard
Quality Level	200
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	Cl.Clc1ccc(OCC(=O)N2CCN(CC2)Cc3ccc4OCOc4c3)cc1
InChI	1S/C20H21ClN2O4.ClH/c21-16-2-4-17(5-3-16)25-13-20(24)23-9-7-22(8-10-23)12-15-1-6-18-19(11-15)27-14-26-18;/h1-6,11H,7-10,12-14H2;1H
InChI key	MVOWQBJZZKOQNU-UHFFFAOYSA-N

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Подробнее

Firocoxib

Empirical Formula (Hill Notation):	C₁₇H₂₀O₅S
CAS Number:	189954-96-9
Molecular Weight:	336.40
Beilstein/REAXYS Number:	8335837
MDL number:	MFCD09837800
PubChem Substance ID:	329754109
NACRES:	NA.24

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	O=S(C1=CC=C(C2=C(OCC3CC3)C(OC2(C)C)=O)C=C1)(C)=O
InChI	1S/C17H20O5S/c1-17(2)14(12-6-8-13(9-7-12)23(3,19)20)15(16(18)22-17)21-10-11-4-5-11/h6-9,11H,4-5,10H2,1-3H3
InChI key	FULAPETWGIGNMT-UHFFFAOYSA-N

192,99 евро / 18 148 руб.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Flubendazole-d3

Empirical Formula (Hill Notation):	C₁₆D₃H₉FN₃O₃
CAS Number:	1173021-08-3
Molecular Weight:	316.30
MDL number:	MFCD11975215
PubChem Substance ID:	329754353
NACRES:	NA.24

Flubendazole-d3 is an isotopically labeled compound of benzimidazole derivative, flubendazole.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Flubendazole-d3 may be used as an internal standard for the determination of flubendazole in animal muscle tissues and sludge samples by ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS).

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
mass shift	M+3
SMILES string	[2H]C([2H])([2H])OC(=O)Nc1nc2cc(ccc2[nH]1)C(=O)c3ccc(F)cc3
InChI	1S/C16H12FN3O3/c1-23-16(22)20-15-18-12-7-4-10(8-13(12)19-15)14(21)9-2-5-11(17)6-3-9/h2-8H,1H3,(H2,18,19,20,22)/i1D3
InChI key	CPEUVMUXAHMANV-FIBGUPNXSA-N

RIDADR	NONH for all modes of transport
WGK Germany	WGK 2

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Подробнее

Flucloxacillin sodium

Empirical Formula (Hill Notation):	C₁₉H₁₆ClFN₃NaO₅S
CAS Number:	1847-24-1
Molecular Weight:	475.85
EC Number:	217-428-0
MDL number:	MFCD01682108
PubChem Substance ID:	329754152
NACRES:	NA.24

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
storage temp.	2-8°C
SMILES string	CC1(C)[C@H](C([O-])=O)N2C([C@@H](NC(C3=C(C)ON=C3C4=C(F)C=CC=C4Cl)=O)[C@@]2([H])S1)=O.[Na+]
InChI	1S/C19H17ClFN3O5S.Na/c1-7-10(12(23-29-7)11-8(20)5-4-6-9(11)21)15(25)22-13-16(26)24-14(18(27)28)19(2,3)30-17(13)24;/h4-6,13-14,17H,1-3H3,(H,22,25)(H,27,28);/q;+1/p-1/t13-,14+,17-;/m1./s1
InChI key	OTEANHMVDHZOPB-SLINCCQESA-M

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Flufenamic acid, a non-steroidal anti-inflammatory drug, is an effective analgesic agent.

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Flufenamic acid

Empirical Formula (Hill Notation):	C₁₄H₁₀F₃NO₂
Linear Formula:	2-(CF₃C₆H₄NH)C₆H₄CO₂H
CAS Number:	530-78-9
Molecular Weight:	281.23
EC Number:	208-494-1
MDL number:	MFCD00002422
PubChem Substance ID:	329799777
NACRES:	NA.24

Flufenamic acid has been used as a standard in studying the two well defined, polymorphs of flufenamic acid like form I and form III, using solid-state density functional theory and terahertz spectroscopy.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard, for drug analysis
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	132-135 °C (lit.)
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	OC(=O)c1ccccc1Nc2cccc(c2)C(F)(F)F
InChI	1S/C14H10F3NO2/c15-14(16,17)9-4-3-5-10(8-9)18-12-7-2-1-6-11(12)13(19)20/h1-8,18H,(H,19,20)
InChI key	LPEPZBJOKDYZAD-UHFFFAOYSA-N

pictograms	GHS06
signalword	Danger
hcodes	H301 - H315 - H319
pcodes	P301 + P310 + P330 - P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

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Flumequine-(1,2,carboxy-13C3)

Empirical Formula (Hill Notation):	¹³C₃C₁₁H₁₂FNO₃
CAS Number:	1185049-09-5
Molecular Weight:	264.23
MDL number:	MFCD28118924
PubChem Substance ID:	329754166
NACRES:	NA.24

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	FC1=CC2=C(N3C(C)CC2)C([13C]([13C]([13C](O)=O)=C3)=O)=C1
InChI	1S/C14H12FNO3/c1-7-2-3-8-4-9(15)5-10-12(8)16(7)6-11(13(10)17)14(18)19/h4-7H,2-3H2,1H3,(H,18,19)/i11+1,13+1,14+1
InChI key	DPSPPJIUMHPXMA-AIGZGMKWSA-N

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Flunixin is classified under the group of non-steroidal anti-inflammatory drugs (NSAIDs).
Flunixin is a potent nonsteroidal anti-inflammatory drug, primarily used as an anti-inflammatory agent and analgesic for the short-term treatment of moderate pain and inflammation in farm animals. It is also effective in inhibiting the synthesis of prostaglandins.

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Flunixin

Empirical Formula (Hill Notation):	C₁₄H₁₁F₃N₂O₂
CAS Number:	38677-85-9
Molecular Weight:	296.24
MDL number:	MFCD00072033
PubChem Substance ID:	329754590
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Flunixin may be used as a reference standard for the determination of NSAID drug, flunixin in biological samples using high-performance liquid chromatography with diode array detection (HPLC-DAD)/particle beam mass spectrometry (PB-MS)/atmospheric pressure ionization mass spectrometry (API-MS) and gas chromatography coupled to mass spectrometry (GC-MS).
Flunixin may be used as an analytical reference standard for the determination of flunixin in:

Bovine muscle samples by hydrophilic interaction liquid chromatography-electrospray-tandem mass spectrometry (HILIC-ESI-MS/MS) equipped with selected reaction monitoring (SRM) detection.
Animal tissues by dispersive-solid phase extraction (d-SPE) and enhanced matrix removal for lipids (EMR-L), followed by analysis using ultra-high performance liquid chromatography-triple quadrupole or quadrupole-time-of-flight (UHPLC-QqQ or UHPLC-Q/TOF) methods in conjunction with ESI-MS/MS operating on multiple reaction monitoring (MRM) mode of detection as well as ESI-LC-MS/MS with SRM detection mode.
Porcine muscle samples by ESI-LC-MS/MS with MRM detection mode.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	Cc1c(Nc2ncccc2C(O)=O)cccc1C(F)(F)F
InChI	1S/C14H11F3N2O2/c1-8-10(14(15,16)17)5-2-6-11(8)19-12-9(13(20)21)4-3-7-18-12/h2-7H,1H3,(H,18,19)(H,20,21)
InChI key	NOOCSNJCXJYGPE-UHFFFAOYSA-N

pictograms	GHS06
signalword	Danger
hcodes	H301
pcodes	P264 - P270 - P301 + P310 - P405 - P501
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fluocinolone acetonide may be used as a reference standard in the analysis of fluocinolone acetonide in samples of soil via pressurized liquid extraction (PLE) and solid-phase extraction (SPE) followed by liquid chromatography coupled with tandem mass spectrometry (LC/MS/MS).

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Fluocinolone acetonide

Empirical Formula (Hill Notation):	C₂₄H₃₀F₂O₆
CAS Number:	67-73-2
Molecular Weight:	452.49
EC Number:	200-668-5
MDL number:	MFCD00010525
PubChem Substance ID:	329799775

Quality Level	100
grade	analytical standard
assay	97.5% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	267-269 °C (lit.)
Featured Industry	Forensics and Toxicology Veterinary
format	neat
SMILES string	CC1(C)O[C@@H]2C[C@H]3[C@@H]4C[C@H](F)C5=CC(=O)C=C[C@]5(C)[C@@]4(F)[C@@H](O)C[C@]3(C)[C@@]2(O1)C(=O)CO
InChI	1S/C24H30F2O6/c1-20(2)31-19-9-13-14-8-16(25)15-7-12(28)5-6-21(15,3)23(14,26)17(29)10-22(13,4)24(19,32-20)18(30)11-27/h5-7,13-14,16-17,19,27,29H,8-11H2,1-4H3/t13-,14-,16-,17-,19+,21-,22-,23-,24+/m0/s1
InChI key	FEBLZLNTKCEFIT-VSXGLTOVSA-N
Gene Information	human ... NR3C1(2908)

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Fluoranthene (FA) is a polycyclic aromatic hydrocarbon, which can be used in the preparation of fluorescent chemosensors for the specific detection of picric acid.
FA, a six ringed highly stable compound, is considered as an environmental indicator. It is mainly selected for simulation study.

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Fluoranthene 48535

Empirical Formula (Hill Notation):	C₁₆H₁₀
CAS Number:	206-44-0
Molecular Weight:	202.25
Beilstein/REAXYS Number:	1907918
EC Number:	205-912-4
MDL number:	MFCD00001184
PubChem Substance ID:	24872062

General description

FA was used after dissolving in HPLC grade acetonitrile, in order to determine retention data and to study the linearity of the detector, during HPLC analysis of PAH (polycyclic aromatic hydrocarbon).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fluoranthene (FA) may also be used as an analytical standard for the determination of the analyte in food samples, oils, fats, and environmental samples by various chromatography techniques.

Quality Level	100
grade	analytical standard
form	neat
CofA	current certificate can be downloaded
packaging	ampule of 5000 mg
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	384 °C (lit.)
mp	105-110 °C (lit.)
Featured Industry	Environmental
format	neat
storage temp.	room temp
SMILES string	c1ccc-2c(c1)-c3cccc4cccc-2c34
InChI	1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H
InChI key	GVEPBJHOBDJJJI-UHFFFAOYSA-N

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H302 - H410
pcodes	P264 - P270 - P273 - P301 + P312 - P391 - P501
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 2
Flash Point F	388.4 °F - closed cup
Flash Point C	198.0 °C - closed cup

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Fluoranthene BCR160R-10MG

Empirical Formula (Hill Notation):	C₁₆H₁₀
CAS Number:	206-44-0
Molecular Weight:	202.25
Beilstein/REAXYS Number:	1907918
EC Number:	205-912-4
MDL number:	MFCD00001184
PubChem Substance ID:	329773796

For more information please see:
BCR160R

BCR is a registered trademark of European Commission

grade	certified reference material
Agency/Method	BCR^®
Торговая марка	JRC
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	384 °C (lit.)
mp	105-110 °C (lit.)
Featured Industry	Environmental Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	c1ccc-2c(c1)-c3cccc4cccc-2c34
InChI	1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H
InChI key	GVEPBJHOBDJJJI-UHFFFAOYSA-N

pictograms	GHS07, GHS09
signalword	Warning
hcodes	H302-H410
pcodes	P273-P501
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 3077 9 / PGIII
WGK Germany	2
Flash Point F	388.4 °F
Flash Point C	198 °C

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Fluorene 48568

Empirical Formula (Hill Notation):	C₁₃H₁₀
CAS Number:	86-73-7
Molecular Weight:	166.22
Beilstein/REAXYS Number:	1363491
EC Number:	201-695-5
MDL number:	MFCD00001111
PubChem Substance ID:	24872116

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fluorene has been used as a test material in studying its electronic transitions in gas and crystalline phases, and in stretched polymer sheets, measured with synchrotron radiation.

Quality Level	100
grade	analytical standard
form	neat
CofA	current certificate can be downloaded
packaging	ampule of 5000 mg
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	298 °C (lit.)
mp	111-114 °C (lit.)
Featured Industry	Environmental
format	neat
storage temp.	room temp
SMILES string	C1c2ccccc2-c3ccccc13
InChI	1S/C13H10/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12/h1-8H,9H2
InChI key	NIHNNTQXNPWCJQ-UHFFFAOYSA-N

pictograms	GHS09
signalword	Warning
hcodes	H410
pcodes	P273 - P501
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 3
Flash Point F	303.8 °F - closed cup
Flash Point C	151.0 °C - closed cup

content (F): 1000 mg / Ampoule
Determination method:Titration with Lanthannitrat solution (traceable to NIST SRM 682)
Accuracy of the method: +/- 2 mg

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Fluoride standard

Titrisol is a registered trademark of Merck KGaA, Darmstadt, Germany

storage conditions	no restrictions.
Quality Level	100
application(s)	ion chromatography: suitable
pH	8.4 (20 °C in H₂O)
density	1.00 g/cm³ at 20 °C
Featured Industry	Environmental Food and Beverages
format	single component solution
storage temp.	15-25°C

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to SI unit kg and measured against primary material from an NMI, e.g. NIST.
Certified content incl. uncertainty and expiry date are given on the label.

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Fluoride Standard for IC

Fluoride standard for IC can be used as standard in the quantitative determination of fluoride impurities in ionic liquids via ion chromatography technique (IC).

1000 mg/L fluoride in water, prepared with high purity NaF and water

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L fluoride in water
application(s)	ion chromatography: suitable
Featured Industry	Environmental Food and Beverages
format	single component solution

Personal Protective Equipment	Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	nwg
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Concentration (F): 990 - 1010 mg/l
Determination method: Titration with Lanthannitrate solution
(traceable to NIST SRM 682)
Accuracy of the method: ± 2 mg/l

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Fluoride standard solution

CERTIPUR is a registered trademark of Merck KGaA, Darmstadt, Germany

storage conditions	Store at +15°C to +25°C.
Quality Level	100
application(s)	ion chromatography: suitable
pH	6 (20 °C in H₂O)
density	1.000 g/cm³ at 20 °C
Featured Industry	Environmental Food and Beverages
format	single component solution
storage temp.	15-25°C

Fluorobenzene is a colorless liquid, which can find applications as a reagent for resin or plastic polymers and also as an insecticide. It also plays the role of a capping agent in the synthesis of a non-fullerene electron acceptor like SF(DPPFB)4 comprising of a spirobifluorene core and four diketopyrrolopyrrole (DPP) arms that can find applications in designing organic solar cells.

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Fluorobenzene

Empirical Formula (Hill Notation):	C₆H₅F
CAS Number:	462-06-6
Molecular Weight:	96.10
Beilstein/REAXYS Number:	1236623
EC Number:	207-321-7
MDL number:	MFCD00000280
PubChem Substance ID:	329757596
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fluorobenzene may be used as an analytical reference standard for the determination of the analyte in cell suspensions of Rhizobiales strain F11, and water samples by liquid chromatography (LC) based techniques. It may also be used as an internal standard for the determination of volatile aromatic compounds in gasoline by comprehensive two-dimensional gas chromatography (GC x GC).

Quality Level	100
grade	analytical standard
assay	99.7% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.465 (lit.), n20/D 1.465
bp	85 °C (lit.)
mp	42 °C (lit.)
density	1.024 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
storage temp.	2-8°C
SMILES string	Fc1ccccc1
InChI	1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H
InChI key	PYLWMHQQBFSUBP-UHFFFAOYSA-N

pictograms	GHS02,GHS05,GHS09
signalword	Danger
hcodes	H225 - H318 - H411
pcodes	P210 - P233 - P240 - P273 - P280 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2387 3 / PGII
WGK Germany	WGK 2
Flash Point F	5.0 °F - closed cup
Flash Point C	-15 °C - closed cup

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Fluorobenzene solution 47895

CAS Number:	462-06-6
EC Number:	200-659-6

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Fluorobenzene may be used as an internal standard for the quantification of volatile organic compounds in environmental samples using chromatography techniques.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
feature	standard type internal
packaging	ampule of 1 mL
concentration	1000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C
InChI	1S/C6H5F/c7-6-4-2-1-3-5-6/h1-5H
InChI key	PYLWMHQQBFSUBP-UHFFFAOYSA-N

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.
Fluorouracil, an analog of the pyrimidines, belongs to the class of antimetabolite drugs. It is generally utilized for the remediation of tumors such as breast adenocarcinoma, gastrointestinal tract, ovary, head and neck.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
RIDADR	UN1230 - class 3 - PG 2 - Methanol
WGK Germany	WGK 2

12,96 евро / 1 219 руб.

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Fluorouracil

Empirical Formula (Hill Notation):	C₄H₃FN₂O₂
CAS Number:	51-21-8
Molecular Weight:	130.08
Beilstein/REAXYS Number:	127172
EC Number:	200-085-6
MDL number:	MFCD00006018
PubChem Substance ID:	329823233
NACRES:	NA.24

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Fluorouracil may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by different analytical techniques.

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

To see an example of a Certificate of Analysis for this material enter LRAC3468 in the slot below. This is an example certificate only and may not be the lot that you receive.

Footnote

Quality Level	300
grade	certified reference material, pharmaceutical secondary standard
form	neat
CofA	current certificate can be downloaded
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	282-286 °C (dec.) (lit.)
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to BP 995, traceable to PhEur F0250000, traceable to USP 12790000
SMILES string	FC1=CNC(=O)NC1=O
InChI	1S/C4H3FN2O2/c5-2-1-6-4(9)7-3(2)8/h1H,(H2,6,7,8,9)
InChI key	GHASVSINZRGABV-UHFFFAOYSA-N
Gene Information	human ... TYMS(7298)

pictograms	GHS06,GHS08
signalword	Danger
hcodes	H301 - H351
pcodes	P201 - P202 - P264 - P270 - P280 - P301 + P310
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3

Этот продукт поставляется в том виде, в каком он был предоставлен и указан выдавшей Фармакопеей. Вся информация, предоставленная в поддержку этого продукта, включая Паспорт безопасности (SDS) и любые информационные листки о продукте, была разработана и выпущена под руководством выдавшей Фармакопеи. Флуоксетина гидрохлорид, селективный ингибитор обратного захвата серотонина, является мощным антидепрессантом.

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Флуоксетин гидрохлорид EDQM

Эмпирическая формула (нотация Хилла):	C₁₇H₁₈F₃NO · HCl
Номер CAS:	56296-78-7
Молекулярный вес:	345.79
Номер MDL:	MFCD00214288
Идентификатор вещества PubChem:	329799646
NACRES:	NA.24

Биохимические/физиологические действия

Селективный ингибитор обратного захвата серотонина; антидепрессант.

Упаковка

Количество единиц: 250 мг. Возможны изменения. Продукт поставляется в том виде, в каком он был предоставлен выдавшей Фармакопеей.

Прочие примечания

Могут применяться ограничения на продажу.

Правовая информация

Продается по лицензии Eli Lilly and Company.
Prozac является зарегистрированной торговой маркой Eli Lilly and Co.

Информация по безопасности

Уровень качества	100
класс	фармацевтический первичный стандарт
форма	чистый
Торговая марка	EDQM
применение	ВЭЖХ: подходит, газовая хроматография (ГХ): подходит
Рекомендуемая отрасль	Фармацевтика
формат	чистый
Строка SMILES	CNCCC(C1=CC=CC=C1)OC2=CC=C(C(F)(F)F)C=C2.[H]Cl
InChI	1S/C17H18F3NO.ClH/c1-21-12-11-16(13-5-3-2-4-6-13)22-15-9-7-14(8-10-15)17(18,19)20;/h2-10,16,21H,11-12H2,1H3;1H
Ключ InChI	GIYXAJPCNFJEHY-UHFFFAOYSA-N
Информация о генах	человек ... SLC6A4(6532)

пиктограммы	GHS05,GHS07,GHS08,GHS09
сигнальное слово	Опасно
коды опасности	H302 - H318 - H336 - H373 - H410
коды предосторожности	P260 - P273 - P280 - P301 + P312 - P305 + P351 + P338 - P314
Целевые органы	Центральная нервная система
RIDADR	UN 3077 9 / PGIII
WGK Германия	WGK 3
Температура вспышки по Фаренгейту	Неприменимо
Температура вспышки по Цельсию	Неприменимо

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Fluoxymesterone

Empirical Formula (Hill Notation):	C₂₀H₂₉FO₃
CAS Number:	76-43-7
Molecular Weight:	336.44
EC Number:	200-961-8
MDL number:	MFCD00010480
PubChem Substance ID:	24894947

Fluoxymesterone is an androgen and anabolic steroid.

biological source	Porcine pancreas, bovine milk (other parts like skeletal muscle/bile/bone/connective tissue/skin), microbial (Mycobacterium sp.)
form	solid (photosensitive)
drug control	USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada
application(s)	HPLC: suitable, gas chromatography (GC): suitable
color	white
solubility	H₂O: 0.5 mg/mL, 45% (w/v) aq 2-hydroxypropyl--cyclodextrin: 6.4 mg/mL, ethanol: 7.3 mg/mL
Featured Industry	Forensics and Toxicology Veterinary
shipped in	ambient
storage temp.	room temp
SMILES string	[H][C@@]12CC[C@](C)(O)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)CC[C@]34C
InChI	1S/C20H29FO3/c1-17-8-6-13(22)10-12(17)4-5-15-14-7-9-19(3,24)18(14,2)11-16(23)20(15,17)21/h10,14-16,23-24H,4-9,11H2,1-3H3/t14-,15-,16-,17-,18-,19-,20-/m0/s1
InChI key	YLRFCQOZQXIBAB-RBZZARIASA-N
Gene Information	human ... AR(367), ESR1(2099), PRLR(5618)

pictograms	GHS08
signalword	Warning
hcodes	H361
pcodes	P281
Personal Protective Equipment	Eyeshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Flupirtine belongs to N-methyl-D-aspartate class of drugs. It is a centrally acting non opioid analgesic with muscle relaxant and neuroprotective properties.

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Flupirtine

Empirical Formula (Hill Notation):	C₁₅H₁₇FN₄O₂
CAS Number:	56995-20-1
Molecular Weight:	304.32
Beilstein/REAXYS Number:	493526
EC Number:	260-503-8
MDL number:	MFCD00864265
PubChem Substance ID:	329756545
NACRES:	NA.24

Flupirtine may be used as a reference drug for the determination of flupirtine in biological samples by liquid chromatography combined with tandem mass spectrometry (HPLC-MS/MS).

grade	analytical standard
Quality Level	100
assay	98.0% (HPLC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
storage temp.	2-8°C
SMILES string	FC1=CC=C(CNC2=NC(N)=C(NC(OCC)=O)C=C2)C=C1
InChI	1S/C15H17FN4O2/c1-2-22-15(21)19-12-7-8-13(20-14(12)17)18-9-10-3-5-11(16)6-4-10/h3-8H,2,9H2,1H3,(H,19,21)(H3,17,18,20)
InChI key	JUUFBMODXQKSTD-UHFFFAOYSA-N

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Formaldehyde dimethyl acetal is formed as a by-product during the production of trioxane, a crucial intermediate for the manufacture of polyacetal plastics.

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BCR490-30G

Fly ash (PCDDs, PCDFs) BCR490-30G

NACRES: NA.24

Analysis Note
For more information please see:
BCR490
Legal Information
BCR is a registered trademark of European Commission
Параметры

grade certified reference material

Agency/Method BCR^®

Торговая марка JRC

Featured Industry Environmental
Pharmaceutical (small molecule)

format matrix material

Safety Information

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Formaldehyde dimethyl acetal

Empirical Formula (Hill Notation):	C₃H₈O₂
Linear Formula:	CH₂(OCH₃)₂
CAS Number:	109-87-5
Molecular Weight:	76.09
Beilstein/REAXYS Number:	1697025
EC Number:	203-714-2
MDL number:	MFCD00008495
PubChem Substance ID:	329769670
NACRES:	NA.24

2-Fluorobiphenyl may be used an analytical standard for the determination of the analyte in surface water samples, chemical raw materials, binary and ternary mixtures with methanol and/or water by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
assay	99.5% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.354
bp	41-43 °C
density	0.860 g/mL at 20 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	COCOC
InChI	1S/C3H8O2/c1-4-3-5-2/h3H2,1-2H3
InChI key	NKDDWNXOKDWJAK-UHFFFAOYSA-N

pictograms	GHS02
signalword	Danger
hcodes	H225
pcodes	P210 - P370 + P378 - P403 + P235
Supp Hazards	EUH019
Personal Protective Equipment	Eyeshields, Faceshields, Gloves
RIDADR	UN1234 - class 3 - PG 2 - Methylal
WGK Germany	WGK 1
Flash Point F	-0.4 °F - closed cup
Flash Point C	-18 °C - closed cup

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Formaldehyde O-pentafluorophenylmethyl-oxime

Empirical Formula (Hill Notation):	C₈H₄F₅NO
CAS Number:	86356-73-2
Molecular Weight:	225.12
MDL number:	MFCD00191477
PubChem Substance ID:	329756120
NACRES:	NA.24

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
assay	98.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	neat
storage temp.	2-8°C
SMILES string	Fc1c(F)c(F)c(CON=C)c(F)c1F
InChI	1S/C8H4F5NO/c1-14-15-2-3-4(9)6(11)8(13)7(12)5(3)10/h1-2H2
InChI key	SRTQFRQWTUMMTC-UHFFFAOYSA-N

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Formaldehyde Oxazolidine solution 48414

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
Agency/Method	NIOSH 2541, OSHA 52
CofA	current certificate can be downloaded
feature	standard type calibration
packaging	ampule of 1 mL
concentration	2000 µg/mL in toluene
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	single component solution
storage temp.	2-8°C

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H225 - H304 - H315 - H336 - H361d - H373 - H412
pcodes	P201 - P210 - P273 - P301 + P310 + P331 - P302 + P352 - P308 + P313
Target Organs	Central nervous system
RIDADR	UN1294 - class 3 - PG 2 - Toluene, solution
WGK Germany	WGK 2
Flash Point F	39.2 °F - closed cup
Flash Point C	4.0 °C - closed cup

1000 mg/L formate in water, prepared with calcium formate and water, filtered through a 0.2 μm membrane filter and stabilized with sodium azide

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Formate Standard for IC

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L formate in water
application(s)	ion chromatography: suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution

RIDADR	NONH for all modes of transport
WGK Germany	nwg
Flash Point F	Not applicable
Flash Point C	Not applicable

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Formestane F2552-1G

Empirical Formula (Hill Notation):	C₁₉H₂₆O₃
CAS Number:	566-48-3
Molecular Weight:	302.41
MDL number:	MFCD00057814
PubChem Substance ID:	24894827
NACRES:	NA.25

1 g in glass bottle

Aromatase inhibitor used as an anti-cancer agent against estrogen-dependent tumors.

biological source	synthetic (organic)
Quality Level	100
assay	98% (HPLC)
form	solid
application(s)	HPLC: suitable, gas chromatography (GC): suitable
solubility	chloroform: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
Featured Industry	Forensics and Toxicology Veterinary
storage temp.	2-8°C
SMILES string	C[C@]12CC[C@H]3[C@@H](CCC4=C(O)C(=O)CC[C@]34C)[C@@H]1CCC2=O
InChI	1S/C19H26O3/c1-18-10-8-15(20)17(22)14(18)4-3-11-12-5-6-16(21)19(12,2)9-7-13(11)18/h11-13,22H,3-10H2,1-2H3/t11-,12-,13-,18+,19-/m0/s1
InChI key	OSVMTWJCGUFAOD-KZQROQTASA-N
Gene Information	human ... CYP19A1(1588)

pictograms	GHS08
signalword	Danger
hcodes	H360
pcodes	P201 - P308 + P313
Personal Protective Equipment	Eyeshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Fosfomycin sodium

Empirical Formula (Hill Notation):	C₃H₅Na₂O₄P
Molecular Weight:	182.02
Beilstein/REAXYS Number:	4604425
EC Number:	247-409-2
MDL number:	MFCD22741288
PubChem Substance ID:	329754806
NACRES:	NA.24

Antibiotic that concentrates in kidney and bladder; reduces nephrotoxicity and ototoxicity of platinum-containing anti-tumor agents. Fosfomycin is a phosphoenolpyruvate analog that irreversibly inhibits UDP-GlcNAc enolpyruvyl tranferase (MurA), an enzyme involved in bacterial cell wall biosynthesis. As a result, the production of N-acetylmuramic acid, an essential element of the peptidoglycan cell wall, is inhibited.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	[Na+].[Na+].C[C@@H]1O[C@@H]1P([O-])([O-])=O
InChI	1S/C3H7O4P.2Na/c1-2-3(7-2)8(4,5)6;;/h2-3H,1H3,(H2,4,5,6);;/q;2*+1/p-2/t2-,3+;;/m0../s1
InChI key	QZIQJIKUVJMTDG-JSTPYPERSA-L

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

For the preparation of this CRM only materials of highest purity were used.

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BCR535-40G

Freshwater harbour sediment (PAHs) BCR535-40G

NACRES: NA.24

Analysis Note
For more information please see:
BCR535
Legal Information
BCR is a registered trademark of European Commission
Параметры

grade certified reference material

Agency/Method BCR^®

Торговая марка JRC

Featured Industry Environmental
Pharmaceutical (small molecule)

format matrix material

storage temp. 2-8°C

Safety Information

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Fructose standard for IC 72669-50ML

1000 mg/L fructose in water, prepared with fructose and water; filtered through a 0.2 μm membrane filter

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
shelf life	limited shelf life, expiry date on the label
concentration	1000 mg/L fructose in water
application(s)	ion chromatography: suitable
Featured Industry	Environmental Food and Beverages
format	single component solution
storage temp.	2-8°C

RIDADR	NONH for all modes of transport
WGK Germany	nwg
Flash Point F	Not applicable
Flash Point C	Not applicable

Fucoxanthin, an abundant marine xanthophyll and a type of sea-weed carotenoid, plays a key role in generating the brown pigment in brown seaweeds. It exhibits pharmacological properties including antitumor and antioxidant properties.

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Fucoxanthin

Empirical Formula (Hill Notation):	C₄₂H₅₈O₆
CAS Number:	3351-86-8
Molecular Weight:	658.91
MDL number:	MFCD01745140
PubChem Substance ID:	329751191
NACRES:	NA.24

Fucoxanthin may be used as an analytical standard for the quantification of the analyte in Undaria pinnatifida using reversed-phase high-performance liquid chromatography (RP-HPLC) technique. Its potential as a selective anticancer agent and an active component for the anti-obesity effect in Undaria lipids is investigated.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Xanthophyll carotenoid pigment extracted from algae. Exhibits anticancer, antioxidant, anti-obesity and anti-inflammatory properties.

Quality Level	100
grade	analytical standard
assay	95.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
storage temp.	20°C
SMILES string	CC(=O)O[C@H]1CC(C)(C)C(=C=C\C(C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(/C)C(=O)C[C@@]23O[C@]2(C)C[C@@H](O)CC3(C)C)[C@](C)(O)C1
InChI	1S/C42H58O6/c1-29(18-14-19-31(3)22-23-37-38(6,7)26-35(47-33(5)43)27-40(37,10)46)16-12-13-17-30(2)20-15-21-32(4)36(45)28-42-39(8,9)24-34(44)25-41(42,11)48-42/h12-22,34-35,44,46H,24-28H2,1-11H3/b13-12+,18-14+,20-15+,29-16+,30-17+,31-19+,32-21+/t23-,34-,35-,40+,41+,42-/m0/s1
InChI key	SJWWTRQNNRNTPU-XJUZQKKNSA-N

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

Fucoxanthinol is the primary metabolite of fucoxanthin, a major marine carotenoid isolated from edible brown seaweeds such as Undaria pinnatifida, Hijikia fusiformis, Laminaria japonica and Sargassum fulvellum with various biological functions. Fucoxanthinol is a compound of significant interest as it exhibits various physiological effects. It is a chemotherapeutic agent that is known to inhibit the growth of human colorectal cancer cells.

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Fucoxanthinol

Empirical Formula (Hill Notation):	C₄₀H₅₆O₅
CAS Number:	7176-02-5
Molecular Weight:	616.87
MDL number:	MFCD18071622
PubChem Substance ID:	329764308
NACRES:	NA.24

Fucoxanthinol may be used as an analytical reference standard for the determination of the analyte in rat plasma by chromatography-based techniques.

grade	analytical standard
Quality Level	100
assay	≥97.0% (HPLC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
format	neat
storage temp.	−20°C
SMILES string	C/C(C=C=C1C(C)(C)C[C@H](O)C[C@]1(O)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C(C[C@@]2(O3)[C@@]3(C)C[C@@H](O)CC2(C)C)=O
InChI	1S/C40H56O5/c1-28(17-13-18-30(3)21-22-35-36(5,6)23-32(41)25-38(35,9)44)15-11-12-16-29(2)19-14-20-31(4)34(43)27-40-37(7,8)24-33(42)26-39(40,10)45-40/h11-21,32-33,41-42,44H,23-27H2,1-10H3/b12-11+,17-13+,19-14+,28-15+,29-16+,30-18+,31-20+/t22-,32-,33-,38+,39+,40-/m0/s1
InChI key	NZEPSBGUXWWWSI-VOPPYBPXSA-N

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.

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Fumaric acid

Empirical Formula (Hill Notation):	C₄H₄O₄
Linear Formula:	HOOCCH=CHCOOH
CAS Number:	110-17-8
Molecular Weight:	116.07
Beilstein/REAXYS Number:	605763
EC Number:	203-743-0
MDL number:	MFCD00002700
eCl@ss:	39021709
PubChem Substance ID:	329767228
E Number:	E297
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
vapor pressure	1.7 mmHg ( 165 °C)
form	neat
autoignition temp.	1364 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	40 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	298-300 °C (subl.) (lit.)
Featured Industry	Cleaning Products Cosmetics Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	OC(=O)\C=C\C(O)=O
InChI	1S/C4H4O4/c5-3(6)1-2-4(7)8/h1-2H,(H,5,6)(H,7,8)/b2-1+
InChI key	VZCYOOQTPOCHFL-OWOJBTEDSA-N

pictograms	GHS07
signalword	Warning
hcodes	H319
pcodes	P264 - P280 - P305 + P351 + P338 - P337 + P313
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 1
Flash Point F	523.4 °F
Flash Point C	273 °C

Furaltadone is a nitrofuran drug, with broad-spectrum antimicrobial activity. It is widely used in veterinary medicine for intensive animal production, especially in pigs, poultry, fish and to provide resistance against infections caused by Escherichia coli and Salmonella.

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Furaltadone

Empirical Formula (Hill Notation):	C₁₃H₁₆N₄O₆
CAS Number:	139-91-3
Molecular Weight:	324.29
Beilstein/REAXYS Number:	8130725
EC Number:	205-384-5
MDL number:	MFCD00057356
PubChem Substance ID:	329757123

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. Furaltadone may be used as an analytical reference standard for the quantification of the analyte in milk samples and poultry eggs using different chromatography techniques.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	200
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	[O-][N+](=O)c1ccc(\C=N\N2CC(CN3CCOCC3)OC2=O)o1
InChI	1S/C13H16N4O6/c18-13-16(14-7-10-1-2-12(22-10)17(19)20)9-11(23-13)8-15-3-5-21-6-4-15/h1-2,7,11H,3-6,8-9H2/b14-7+
InChI key	YVQVOQKFMFRVGR-VGOFMYFVSA-N

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Furan is a clear and colorless liquid, and a bimolecular heterocycle, which can be used to trap unstable intermediates containing highly reactive species, via Diels-Alder cycloaddition reactions.
Furan, a naturally occurring compound associated with the flavor of food, is found at very low levels in a variety of food products and beverages. It finds applications as a solvent for resins and lacquers as well as in the preparation of organic compounds, in pharmaceuticals, etc. Furan is also reportedly identified in heat treated food products, including cooked chicken, fish protein concentrate, caramel back, canned meat, bread, coffee, etc.

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Furan

Empirical Formula (Hill Notation):	C₄H₄O
CAS Number:	110-00-9
Molecular Weight:	68.07
Beilstein/REAXYS Number:	103221
EC Number:	203-727-3
MDL number:	MFCD00003222
PubChem Substance ID:	329756415

Furan may be used as an analytical reference standard for the quantification of the analyte in heat-processed foods using gas chromatography-mass spectrometry (GC-MS).
Furan can undergo Diels-Alder [4+2] cycloaddition reaction with maleic anhydride to form the corresponding exo and endo furan-maleic anhydride adducts.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
vapor density	2.35 (vs air)
vapor pressure	1672 mmHg ( 55 °C), 31.66 psi ( 55 °C), 493 mmHg ( 20 °C), 9.22 psi ( 20 °C)
assay	98.0% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
contains	~0.025% 2,6-di-tert-4-methylphenol as stabilizer
expl. lim.	14.3 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.421 (lit.), n20/D 1.421
bp	32 °C/758 mmHg (lit.)
density	0.936 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
storage temp.	2-8°C
SMILES string	c1ccoc1
InChI	1S/C4H4O/c1-2-4-5-3-1/h1-4H
InChI key	YLQBMQCUIZJEEH-UHFFFAOYSA-N

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H224 - H302 + H332 - H315 - H341 - H350 - H373 - H412
pcodes	P210 - P233 - P273 - P304 + P340 + P312 - P308 + P313 - P403 + P233
Supp Hazards	EUH019
RIDADR	UN 2389 3 / PGI
WGK Germany	WGK 3
Flash Point F	-32.8 °F - closed cup
Flash Point C	-36 °C - closed cup

Furazolidone is an effective antiprotozoal and antibacterial agent.

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Furazolidone

Empirical Formula (Hill Notation):	C₈H₇N₃O₅
CAS Number:	67-45-8
Molecular Weight:	225.16
Beilstein/REAXYS Number:	8317414
EC Number:	200-653-3
MDL number:	MFCD00010550
PubChem Substance ID:	329757127
NACRES:	NA.24

Furazolidone may be used as a reference standard:

For the determination of the analyte in pharmaceutical formulations by second-derivative spectrophotometry.
For the determination of the analyte in animal feeds using liquid chromatography with ultraviolet and thermospray mass spectrometric detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	200
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Clinical Cosmetics Food and Beverages Forensics and Toxicology Personal Care Pharmaceutical (small molecule)
Mode of action	enzyme \| inhibits
antibiotic activity spectrum	Gram-positive bacteria, parasites
format	neat
SMILES string	[O-][N+](=O)c1ccc(\C=N\N2CCOC2=O)o1
InChI	1S/C8H7N3O5/c12-8-10(3-4-15-8)9-5-6-1-2-7(16-6)11(13)14/h1-2,5H,3-4H2/b9-5+
InChI key	PLHJDBGFXBMTGZ-WEVVVXLNSA-N

pictograms	GHS08
signalword	Warning
hcodes	H361fd - H412
pcodes	P201 - P202 - P273 - P280 - P308 + P313 - P405
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

Furazolidone-d4 is an isotopically labeled compound typically used for the quantitation of furazolidone.

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Furazolidone-d4

Empirical Formula (Hill Notation):	C₈D₄H₃N₃O₅
CAS Number:	1217222-76-8
Molecular Weight:	229.18
MDL number:	MFCD04973442
PubChem Substance ID:	329754260
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Furazolidone-d4 may be used as an internal standard for the determination of furazolidone in pig muscle, liver and kidney tissues by high performance liquid chromatography-ultraviolet detection (HPLC-UV) and LC coupled to tandem mass spectrometry (MS/MS).

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
mass shift	M+4
SMILES string	[2H]C1([2H])OC(=O)N(\N=C\c2ccc(o2)[N+]([O-])=O)C1([2H])[2H]
InChI	1S/C8H7N3O5/c12-8-10(3-4-15-8)9-5-6-1-2-7(16-6)11(13)14/h1-2,5H,3-4H2/b9-5+/i3D2,4D2
InChI key	PLHJDBGFXBMTGZ-QIBFQDEWSA-N