C94807
3-Pyridinecarbonitrile
98%
Synonym(s):
3-Cyanopyridine, Nicotinic acid nitrile, Nicotinonitrile
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All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C6H4N2
CAS Number:
Molecular Weight:
104.11
Beilstein:
107711
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
crystals
impurities
<2.5% acetone
bp
201 °C (lit.)
mp
48-52 °C (lit.)
SMILES string
N#Cc1cccnc1
InChI
1S/C6H4N2/c7-4-6-2-1-3-8-5-6/h1-3,5H
InChI key
GZPHSAQLYPIAIN-UHFFFAOYSA-N
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
190.4 °F
Flash Point(C)
88 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Li-Qun Jin et al.
New biotechnology, 28(6), 610-615 (2011-05-10)
2-Chloronicotinic acid is receiving much attention for its effective applications as a key precursor in the synthesis of pesticides and medicines. In this study, a strain ZJB-09149 converting 2-chloro-3-cyanopyridine to 2-chloronicotinic acid was newly isolated and identified as Rhodococcus erythropolis
Haiyang Fan et al.
Bioprocess and biosystems engineering, 40(8), 1271-1281 (2017-06-07)
A novel aliphatic nitrilase, REH16, was found in Ralstonia eutropha H16 and overexpressed in Escherichia coli BL21(DE3), and its enzymatic properties were studied. The temperature and pH optima were 37 °C and 6.6, respectively, and the best thermostability of the nitrilase
Anirban Banerjee et al.
Biotechnology and applied biochemistry, 37(Pt 3), 289-293 (2003-01-29)
A rapid, simple and sensitive fluorometric assay method for the determination of nitrilase activity is described. 3-Cyanopyridine was hydrolysed to nicotinic acid by Rhodococcus rhodochrous and the liberated NH(3) was allowed to react with buffered o -phthaldialdehyde-2-mercaptoethanol solution (pH 7.4)
H Adolfsson et al.
The Journal of organic chemistry, 65(25), 8651-8658 (2000-12-12)
The epoxidation of alkenes with 30% aqueous hydrogen peroxide is catalyzed efficiently by methyltrioxorhenium (MTO) in the presence of pyridine additives. The addition of 1-10 mol % of 3-cyanopyridine increases the system's efficiency for terminal and trans-disubstituted alkenes resulting in
Synthesis and antihistaminic activity of 2-guanadino-3-cyanopyridines and pyrido[2,3-d]-pyrimidines.
J M Quintela et al.
Bioorganic & medicinal chemistry, 5(8), 1543-1553 (1997-08-01)
2-Guanadino-3-cyanopyridines 8-33 and pyrido[2,3-d]-pyrimidines 35-52 were synthesized by nucleophilic displacement and cyclization of the chloroamidines 6a-d easily obtained by reaction of 2-aminocyanopyridines 5a-d with phosgene iminium chloride and their action on the release of histamine by mast cells examined under
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