P62208
3-Pyridinecarboxaldehyde
98%
Synonym(s):
Nicotinaldehyde
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About This Item
Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
Molecular Weight:
107.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-900-4
Beilstein/REAXYS Number:
105343
MDL number:
Assay:
98%
InChI key
QJZUKDFHGGYHMC-UHFFFAOYSA-N
InChI
1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H
SMILES string
[H]C(=O)c1cccnc1
assay
98%
Quality Level
refractive index
n20/D 1.549 (lit.)
bp
78-81 °C/10 mmHg (lit.)
density
1.141 g/mL at 20 °C (lit.)
storage temp.
2-8°C
Related Categories
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
95.0 °F - closed cup
flash_point_c
35 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Jarrod B French et al.
Biochemistry, 49(49), 10421-10439 (2010-10-29)
Nicotinamidases are metabolic enzymes that hydrolyze nicotinamide to nicotinic acid. These enzymes are widely distributed across biology, with examples found encoded in the genomes of Mycobacteria, Archaea, Eubacteria, Protozoa, yeast, and invertebrates, but there are none found in mammals. Although
C C Shone et al.
Biochemistry, 20(26), 7494-7501 (1981-12-22)
Coenzyme A linked aldehyde dehydrogenase from Escherichia coli strain B has been purified to a specific activity of 14 units/mg of protein, and initial rate and substrate analogue inhibition experiments have been performed. On the basis of these steady-state measurements
P Narender et al.
Bioorganic & medicinal chemistry, 14(13), 4600-4609 (2006-03-03)
Baylis-Hillman acetates were synthesized from substituted 2-chloronicotinaldehydes and were conveniently transformed into multisubstituted quinolines and cyclopenta[g]quinolines on reaction with nitroethane or ethyl cyanoacetate via a successive S(N)2'-S(N)Ar elimination strategy. Thus, synthesized quinolines were evaluated for antimicrobial activity and found having
[Selenazoles. X. [1]. Beta-methyl-beta-4-R-selenazolyl-2)-hydrazones of acetaldehyde, benzaldehyde, isonicotinaldehyde, nicotinaldehyde and picolinaldehyde].
S Biliński et al.
Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina, 39, 33-40 (1984-01-01)
K S De Jongh et al.
The Biochemical journal, 242(1), 143-150 (1987-02-15)
The kinetic mechanism of the major sheep liver aldehyde reductase (ALR1) was studied with three aldehyde substrates: p-nitrobenzaldehyde, pyridine-3-aldehyde and D-glucuronate. In each case the enzyme mechanism was sequential and product-inhibition studies were consistent with an ordered Bi Bi mechanism
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