推荐产品
蒸汽壓力
64 mmHg ( 20 °C)
化驗
99%
包含
50 ppm monomethyl ether hydroquinone as inhibitor
折射率
n20/D 1.400 (lit.)
bp
90-92 °C (lit.)
mp
−35.8 °C (lit.)
密度
0.8 g/mL at 25 °C (lit.)
SMILES 字串
CC(=C)C#N
InChI
1S/C4H5N/c1-4(2)3-5/h1H2,2H3
InChI 密鑰
GYCMBHHDWRMZGG-UHFFFAOYSA-N
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訊號詞
Danger
危險分類
Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 1
標靶器官
Central nervous system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 2
閃點（°F）
53.6 °F - closed cup
閃點（°C）
12 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Cytotoxicity of methacrylonitrile.
V Vasanthakumari et al.
Bulletin of environmental contamination and toxicology, 59(2), 274-278 (1997-08-01)
Mohammed Y H Farooqui et al.
Research communications in molecular pathology and pharmacology, 120-121(1-6), 79-92 (2007-01-01)
This study reports the toxicity and metabolism of methacrylonitrile (MeAN) in normal male Sprague-Dawley rats and those pre-treated with caffeine, alcohol or both. Rats were divided into groups often. One group received an oral dose by gavage of 6 %
B I Ghanayem
Toxicity report series, (47)(47), 1-56 (2002-01-24)
Methacrylonitrile is an aliphatic nitrile used extensively in the preparation of homo- and copolymers, elastomers, and plastics and as a chemical intermediate in the preparation of acids, amides, esters, and other nitriles. This aliphatic nitrile is also used as a
Birgit Grill et al.
Molecules (Basel, Switzerland), 25(11) (2020-06-03)
Nitrile hydratases (NHase) catalyze the hydration of nitriles to the corresponding amides. We report on the heterologous expression of various nitrile hydratases. Some of these enzymes have been investigated by others and us before, but sixteen target proteins represent novel
B I Ghanayem et al.
Drug metabolism and disposition: the biological fate of chemicals, 24(4), 390-394 (1996-04-01)
Methacrylonitrile (MAN) is structurally similar to the known carcinogen acrylonitrile (AN), has similar industrial uses, and is occasionally used as its replacement. In contrast to AN, minimal information is available on the toxicity, carcinogenicity, or metabolism of MAN. Earlier work
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