A21401
4-Acetylpyridine
97%
Synonym(s):
Methyl 4-pyridyl ketone
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About This Item
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.529 (lit.)
SMILES string
CC(=O)c1ccncc1
InChI
1S/C7H7NO/c1-6(9)7-2-4-8-5-3-7/h2-5H,1H3
InChI key
WMQUKDQWMMOHSA-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
219.2 °F - closed cup
Flash Point(C)
104 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Journal of biochemistry, 125(1), 41-47 (1999-01-09)
An enzyme responsible for the ketone-reduction of 4-benzoylpyridine (4BP) was purified 350-fold to homogeneity from the cytosolic fraction of rabbit heart. The purified enzyme exhibited a molecular mass of 110 kDa on gel filtration, and 27 kDa on SDS-PAGE, indicating
Biochemistry and molecular biology international, 33(5), 893-899 (1994-08-01)
A correlation was observed between the values of specificity constant (kcat/Km) of carbonyl reductase from rabbit liver for acetohexamide analogs and their partition coefficients. This result indicates that the hydrophobicity in straight-chain alkyl groups of acetohexamide analogs plays an important
Biochemistry and molecular biology international, 31(6), 1105-1110 (1993-12-01)
Carbonyl reductase from rabbit kidney was rapidly inactivated by diethylpyrocarbonate (DEPC). A similar inactivation was observed in photooxidation of the enzyme by methylene blue. The inactivation by DEPC was time- and concentration-dependent and followed pseudo-first-order kinetics. The results obtained from
Neuroscience letters, 85(1), 110-112 (1988-02-15)
4-Acetylpyridine, earlier reported by us to be an anticonvulsant, offers long-lasting protection after a single administration against hypothermic restraint stress-induced gastric ulceration in mice. Electroshock convulsions, marginally but not significantly protective against such ulcers themselves, when coupled with 4-acetylpyridine administration
Brain research, 481(2), 356-360 (1989-03-06)
Measurements of striatal choline acetyltransferase (ChAT) and glutamic acid decarboxylase (GAD) activities indicated that systemic administration of 4-8 mg/kg of MK-801 to rats completely blocked neuronal damage due to intrastriatal injections of 75-150 nmol of quinolinic acid. Similar experiments with
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