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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.495 (lit.)
bp
204 °C (lit.)
density
1.02 g/mL at 25 °C (lit.)
SMILES string
Cc1cc[nH]n1
InChI
1S/C4H6N2/c1-4-2-3-5-6-4/h2-3H,1H3,(H,5,6)
InChI key
XKVUYEYANWFIJX-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - STOT RE 2
Target Organs
Lungs
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point(F)
218.3 °F - closed cup
Flash Point(C)
103.5 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Die Pharmazie, 43(1), 29-31 (1988-01-01)
The release behaviour of the antimicrobially active 3(5)-methylpyrazole from matrix systems prepared from maleic anhydride copolymers as well as from copolymers of maleic esters and maleic amides was studied. Under alkaline conditions erosion is the predominant release mechanism compared to
Die Pharmazie, 40(8), 548-552 (1985-08-01)
The release of 3-methylpyrazole from monolithic polymer films into aqueous media has been studied. The diffusion of the active agent decreased with increasing of the content of acetate groups in reacetylated poly(vinyl alcohols) and with increasing of the ester lengths
Die Pharmazie, 41(2), 118-120 (1986-02-01)
The diffusion of 3-methylpyrazole through a synthetic polymer matrix and the effect of the solubility of the bioactive agent in polymers on the release behaviour of polymer combinations were studied. With increasing hydrophilicity of the polymer both the diffusion and
Extremely long protection by pyrazole derivatives against chemically induced gastric mucosal injury.
The Journal of pharmacology and experimental therapeutics, 256(2), 592-598 (1991-02-01)
We tested the hypothesis that the gastrotoxicity of ethanol and other damaging agents is influenced through the modulation of alcohol dehydrogenase (ADH) by using either the ADH-inhibitor pyrazole or the noninhibitor derivatives of pyrazole. In time course experiments, the protection
Journal of cancer research and clinical oncology, 113(2), 145-150 (1987-01-01)
Using a hybrid ion-exchange reverse phase HPLC system, we found that F344 rat liver microsomes, in the presence of an NADPH-generating system, can metabolize methylazoxymethanol (MAM), a colon and liver carcinogen, to methanol and formic acid. This is in contrast
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