Skip to Content
Merck
All Photos(1)

Documents

349496

Sigma-Aldrich

Pyrazinecarbonitrile

99%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H3N3
CAS Number:
Molecular Weight:
105.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.534 (lit.)

bp

87 °C/6 mmHg (lit.)

density

1.174 g/mL at 25 °C (lit.)

SMILES string

N#Cc1cnccn1

InChI

1S/C5H3N3/c6-3-5-4-7-1-2-8-5/h1-2,4H

InChI key

PMSVVUSIPKHUMT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

206.6 °F - closed cup

Flash Point(C)

97 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Reductive decyanation of pyrazinecarbonitriles.
Albaneze-Walker J, et al.
Tetrahedron Letters, 43(38), 6747-6750 (2002)
Il Woong Baek et al.
Journal of nanoscience and nanotechnology, 10(10), 6939-6943 (2010-12-09)
We have fabricated fluorescing polystyrene/dicyanopyrazine-linked porphyrin (PS/4-TDCPP) nanofibers using the electrospinning technique. UV-vis spectroscopy shows a strong Soret band and two relatively weak Q bands from the PS/4-TDCPP films and fibers, and reveals that the 4-TDCPP molecules are homogeneously dispersed
Derrick R Seiner et al.
Biochemistry, 49(44), 9613-9619 (2010-10-01)
Nicotinamidase/pyrazinamidase (PncA) is involved in the NAD+ salvage pathway of Mycobacterium tuberculosis and other bacteria. In addition to hydrolyzing nicotinamide into nicotinic acid, PncA also hydrolyzes the prodrug pyrazinamide to generate the active form of the drug, pyrazinoic acid, which
M Kobayashi et al.
The Journal of antibiotics, 43(10), 1316-1320 (1990-10-01)
Using resting cells of Rhodococcus rhodochrous J1, in which a large amount of nitrilase is induced, a simple and efficient bioconversion process for the production of pyrazinoic acid, an antimycobacterial agent, through catalysis by a nitrilase was developed. The reaction
Synthesis, structure, network and thermal analysis of four 5-(pyrazinyl) tetrazolato copper (II) and cobalt (II) complexes.
Abu-Youssef MAM, et al.
Polyhedron, 26(7), 1531-1540 (2007)

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