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C94807

Sigma-Aldrich

3-Pyridinecarbonitrile

98%

Sinónimos:

3-Cyanopyridine, Nicotinic acid nitrile, Nicotinonitrile

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About This Item

Fórmula empírica (notación de Hill):
C6H4N2
Número de CAS:
100-54-9
Peso molecular:
104.11
Beilstein/REAXYS Number:
107711
EC Number:
202-863-0
MDL number:
MFCD00006372
UNSPSC Code:
12352100
PubChem Substance ID:
24893001
NACRES:
NA.22

Quality Level

100

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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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

190.4 °F

flash_point_c

88 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCM7188
WXBD0871V
MKCD8064
MKCC2773
MKBX6583V

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Win-Long Chia et al.
International journal of molecular sciences, 14(9), 18809-18823 (2013-09-17)
A new series of teraryl 2-(4'-alkoxybiphen-4-yl)-5-cyanopyridines (nO-PPPyCN, n = 2-8) compounds, bearing a cyanopyridine terminus, were synthesized using a short 2-step reaction with overall yields between 33% and 69%. Spectral analyses were in accord with the expected structures. Thermotropic behavior
Mika Takahashi et al.
Reproductive toxicology (Elmsford, N.Y.), 35, 7-16 (2012-11-21)
Crl:CD(SD)rats were given 3-cyanopyridine by gavage at 0, 5, 30 or 180 mg/kg/day. Males were dosed for 42 days beginning 14 days before mating, and females for 40-53 days beginning 14 days before mating to day 3 of lactation, including
Xiaolin Pei et al.
Biotechnology letters, 35(9), 1419-1424 (2013-04-24)
A nitrile hydratase (NHase) gene from Aurantimonas manganoxydans, cloned and expressed in Escherichia coli, gave an enzyme that efficiently hydrated 3-cyanopyridine to nicotinamide with high thermal stability. We have now found that adding Co(2+) at 0.1 mM to LB medium was
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
Y Kato et al.
Archives of microbiology, 170(2), 85-90 (1998-07-31)
A bacterial strain capable of utilizing E-pyridine-3-aldoxime as a nitrogen source was isolated from soil after a 4-month acclimation period and was identified as Rhodococcus sp. The strain contained a novel aldoxime dehydration activity that catalyzed a stoichiometric dehydration of
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