A21401
4-Acetylpyridine
97%
Synonym(s):
Methyl 4-pyridyl ketone
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About This Item
Empirical Formula (Hill Notation):
C7H7NO
CAS Number:
Molecular Weight:
121.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-350-9
Beilstein/REAXYS Number:
107629
MDL number:
Assay:
97%
Form:
liquid
Product Name
4-Acetylpyridine, 97%
InChI
1S/C7H7NO/c1-6(9)7-2-4-8-5-3-7/h2-5H,1H3
InChI key
WMQUKDQWMMOHSA-UHFFFAOYSA-N
SMILES string
CC(=O)c1ccncc1
assay
97%
form
liquid
refractive index
n20/D 1.529 (lit.)
bp
212 °C (lit.)
mp
13-16 °C (lit.)
density
1.095 g/mL at 25 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Y Imamura et al.
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
Y Imamura et al.
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
A Topacli et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(7), 1385-1391 (2001-07-12)
The normal coordinate analysis has been performed for 4-aminopyridine (4-apy) assuming C2v molecular symmetry. A Urey-Bradley force field has been used. The force constants are adjusted to fit the observed frequencies for 4-apy and its deuterated species. The vibrational assignment
S G Zhu et al.
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
Y Imamura et al.
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
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