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4-METHYL-1H-PYRAZOLE HYDROCHLORIDE structure, CAS 56010-88-9

4-METHYL-1H-PYRAZOLE HYDROCHLORIDE

CAS Number56010-88-9

SynonymsFomepizole Hydrochloride; MFCD00012707; 4-methyl-1H-pyrazole,hydrochloride

Molecular FormulaC4H7ClN2

Molecular Weight118.56

Purity≥95%

Density

Boiling Point

Melting Point157-159 °C

Flash Point

Appearancepowder

EINECS0

MSDSChineseEnglish

Symboltransportation

Signal WordWarning

Cat. No.: 2A-0140417 Purity: ≥95%
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Quality Control of [ 56010-88-9 ] Purity: ≥95% SDS Specification MoL

Chemical & Physical Properties
CAS Number56010-88-9
Catalog No.2A-0140417
Chinese Name4-甲基吡唑盐酸盐
SynonymsFomepizole Hydrochloride; MFCD00012707; 4-methyl-1H-pyrazole,hydrochloride
Molecular FormulaC4H7ClN2
Molecular Weight118.56
Purity≥95
Melting Point157-159 °C
Appearancepowder
Storage Conditionroom temperature
ApplicationFormopyrazole hydrochloride (4-methylpyrazole) is a potent inhibitor of cytochrome P450 (CYP2E1). Formopyrazole hydrochloride is a competitive inhibitor of alcohol dehydrogenase. Formopyrazole hydroch
EINECS0
HTC2933199090
UN(IATA)0
PubChem ID24278534
MDL NumberMFCD00012707
SMILESCl.Cc1cn[nH]c1
InChI1S/C4H6N2.ClH/c1-4-2-5-6-3-4;/h2-3H,1H3,(H,5,6);1H
InChI KeyPUCXJHNDMYZOHG-UHFFFAOYSA-N
NACRES CodeNA.77
UNSPSC12352100
Hazard Symbolstransportation
MSDSmsds/140417_1_56010_88_9.pdf
BioactivityFomepizole (4-Methylpyrazole) hydrochloride is a potent cytochrome P450 (CYP2E1) inhibitor. Fomepizole hydrochloride is a competitive inhibitor of the enzyme alcohol dehydrogenase. Fomepizole hydrochloride blocks further conversion of methanol and ethylene glycol to toxic metabolites. Fomepizole hydrochloride has the potential for an antidote for ethylene glycol or methanol poisoning[1][2][3]. Related Catalog Signaling Pathways >> Metabolic Enzyme/Protease >> Cytochrome P450 Research Areas >> Metabolic Disease Target CYP2E1 In Vivo Pretreatment with Fomepizole (4-Methylpyrazole; 25 mg/kg; IP) prolongs ethanol neurobehavioral toxicity in CD-1 mice[4] Animal Model: Male CD-1 mice weighing 18-25 g[4] Dosage: 25 mg/kg Administration: IP; single dose Result: Decreased the dose of ethanol (1-5 g/kg; IP) at which 50% of the animals failed a particular outcome test (toxic dose 50; TD50). References [1]. Casavant MJ. Fomepizole in the treatment of poisoning. Pediatrics. 2001 Jan;107(1):170. [2]. Lepik KJ, et al. Adverse drug events associated with the antidotes for methanol and ethylene glycol poisoning: a comparison of ethanol and fomepizole. Ann Emerg Med. 2009 Apr;53(4):439-450.e10. [3]. Garrett Rampon, et al. Use of fomepizole as an adjunct in the treatment of acetaminophen overdose: a case series. Toxicology Communications. Volume 4, 2020 - Issue 1. [4]. Páez AM, et al. Effects of 4-methylpyrazole on ethanol neurobehavioral toxicity in CD-1 mice. Acad Emerg Med. 2004 Aug;11(8):820-6. Chemical & Physical Properties Melting Point 157-159 °C Molecular Formula C4H7ClN2 Molecular Weight 118.56500 Exact Mass 118.03000 PSA 28.68000 LogP 1.52010 InChIKey PUCXJHNDMYZOHG-UHFFFAOYSA-N SMILES Cc1cn[nH]c1.Cl
Use ofFomepizole (4-Methylpyrazole) hydrochloride is a potent cytochrome P450 (CYP2E1) inhibitor. Fomepizole hydrochloride is a competitive inhibitor of the enzyme alcohol dehydrogenase. Fomepizole hydrochloride blocks further conversion of methanol and ethylene glycol to toxic metabolites. Fomepizole hydrochloride has the potential for an antidote for ethylene glycol or methanol poisoning[1][2][3]. Properties Articles34 Name 4-Methylpyrazole hydrochloride Synonym More Synonyms 4-Methylpyrazole hydrochloride Biological Activity Description Fomepizole (4-Methylpyrazole) hydrochloride is a potent cytochrome P450 (CYP2E1) inhibitor. Fomepizole hydrochloride is a competitive inhibitor of the enzyme alcohol dehydrogenase. Fomepizole hydrochloride blocks further conversion of methanol and ethylene glycol to toxic metabolites. Fomepizole hydrochloride has the potential for an antidote for ethylene glycol or methanol poisoning[1][2][3]. Related Catalog Signaling Pathways >> Metabolic Enzyme/Protease >> Cytochrome P450 Research Areas >> Metabolic Disease References [1]. Casavant MJ. Fomepizole in the treatment of poisoning. Pediatrics. 2001 Jan;107(1):170. [2]. Lepik KJ, et al. Adverse drug events associated with the antidotes for methanol and ethylene glycol poisoning: a comparison of ethanol and fomepizole. Ann Emerg Med. 2009 Apr;53(4):439-450.e10. [3]. Garrett Rampon, et al. Use of fomepizole as an adjunct in the treatment of acetaminophen overdose: a case series. Toxicology Communications. Volume 4, 2020 - Issue 1. Chemical & Physical Properties Exact Mass 118.03000 PSA 28.68000 LogP 1.52010 InChIKey PUCXJHNDMYZOHG-UHFFFAOYSA-N
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Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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