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195413

Sigma-Aldrich

Methacrylonitrile

99%

Synonym(s):

1-Methylethenyl cyanide, 2-Cyano-1-propene, 2-Methyl-2-propenenitrile, 2-Methylpropenenitrile, Isobutenenitrile, Isopropene cyanide, Methacrylnitrile

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About This Item

Linear Formula:
CH2=C(CH3)CN
CAS Number:
Molecular Weight:
67.09
Beilstein:
773708
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:

vapor pressure

64 mmHg ( 20 °C)

Assay

99%

contains

50 ppm monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.400 (lit.)

bp

90-92 °C (lit.)

mp

−35.8 °C (lit.)

density

0.8 g/mL at 25 °C (lit.)

SMILES string

CC(=C)C#N

InChI

1S/C4H5N/c1-4(2)3-5/h1H2,2H3

InChI key

GYCMBHHDWRMZGG-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 1

Target Organs

Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

53.6 °F - closed cup

Flash Point(C)

12 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Directed organic grafting on locally doped silicon substrates.
Julienne Charlier et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 6(1), 70-74 (2005-02-04)
Kamila Rzeznicka et al.
Applied microbiology and biotechnology, 85(5), 1417-1425 (2009-08-08)
The nitrile hydratase (NHase, EC 4.2.1.84) genes (alpha and beta subunit) and the corresponding activator gene from Rhodococcus equi TG328-2 were cloned and sequenced. This Fe-type NHase consists of 209 amino acids (alpha subunit, M(r) 23 kDa) and 218 amino
A Zeenath Unnisa et al.
Drug and chemical toxicology, 28(2), 187-195 (2005-05-04)
The status of brain antioxidant enzymes and glutathione in methacrylonitrile (MeAN)-intoxicated Wistar rats was correlated with the levels of lipid peroxidation products. Optimum changes were observed 30 min and 60 min after oral administration of MeAN at dosages of 50
Effect of methacrylonitrile on rat lung antioxidant enzymes.
T Samikkannu et al.
Bulletin of environmental contamination and toxicology, 59(6), 894-900 (1997-12-24)
Hongbing Wang et al.
Journal of toxicology and environmental health. Part A, 65(7), 523-537 (2002-04-10)
Tissue-specific induction of cytochrome P-450s (CYP) followed by increased in situ bioactivation may contribute to chemical-induced site-specific toxicity. In rats, methacrylonitrile (MAN) is metabolized by cytochrome P-450 2E1 (CYP2E1) to acetone, which is eliminated along with parent MAN in breath.

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