M75802
3-甲基吡唑
97%
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关于此项目
经验公式（希尔记法）:
C4H6N2
化学文摘社编号:
分子量:
82.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
215-925-7
Beilstein/REAXYS Number:
1454
MDL number:
Assay:
97%
Form:
liquid
InChI key
XKVUYEYANWFIJX-UHFFFAOYSA-N
InChI
1S/C4H6N2/c1-4-2-3-5-6-4/h2-3H,1H3,(H,5,6)
SMILES string
Cc1cc[nH]n1
assay
97%
form
liquid
Quality Level
bp
204 °C (lit.)
density
1.02 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1B - STOT RE 2
target_organs
Lungs
存储类别
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
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
B Schulz et al.
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
B Schulz et al.
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
B Schulz et al.
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
Extremely long protection by pyrazole derivatives against chemically induced gastric mucosal injury.
J Hauser et al.
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
E S Fiala et al.
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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