P62208
3-Pyridinecarboxaldehyde
98%
Synonym(s):
Nicotinaldehyde
Sign Into View Organizational & Contract Pricing
Select a Size
About This Item
Empirical Formula (Hill Notation):
C6H5NO
CAS Number:
Molecular Weight:
107.11
Beilstein:
105343
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
98%
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
SMILES string
[H]C(=O)c1cccnc1
InChI
1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H
InChI key
QJZUKDFHGGYHMC-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
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 Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
95.0 °F - closed cup
Flash Point(C)
35 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Hugo Destaillats et al.
Environmental science & technology, 40(6), 1799-1805 (2006-03-31)
Assessment of secondhand tobacco smoke exposure using nicotine as a tracer or biomarker is affected by sorption of the alkaloid to indoor surfaces and by its long-term re-emission into the gas phase. However, surface chemical interactions of nicotine have not
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
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
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
[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)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service