D77001
Adiponitrile
99%
동의어(들):
1,6-hexanedinitrile, ADN, 1,4-Dicyanobutane
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
Linear Formula:
NC(CH2)4CN
CAS 번호:
Molecular Weight:
108.14
Beilstein:
1740005
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
vapor density
3.7 (vs air)
Quality Level
vapor pressure
0.01 mmHg ( 40 °C)
분석
99%
양식
liquid
autoignition temp.
1022 °F
expl. lim.
4.99 %
refractive index
n20/D 1.438 (lit.)
bp
295 °C (lit.)
mp
1-3 °C (lit.)
density
0.951 g/mL at 25 °C (lit.)
SMILES string
N#CCCCCC#N
InChI
1S/C6H8N2/c7-5-3-1-2-4-6-8/h1-4H2
InChI key
BTGRAWJCKBQKAO-UHFFFAOYSA-N
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관련 카테고리
애플리케이션
Adiponitrile is a key precursor for manufacturing nylon-6,6. It can undergo catalytic hydrogenation to form hexamethylenediamine (HMD). ADN shows promising potential as a solvent for electrolyte solutions used in high-voltage lithium batteries due to its high anodic and thermal stability.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 1
Flash Point (°F)
325.4 °F - closed cup
Flash Point (°C)
163 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Inhalation toxicity of adiponitrile in rats.
L W Smith et al.
Toxicology and applied pharmacology, 65(2), 257-263 (1982-09-15)
Jian-Jun Dai et al.
ChemSusChem, 5(4), 617-620 (2012-03-24)
Current affairs: Adiponitrile, used to produce nylon 6.6, is prepared from the renewable compound glutamic acid by an electrochemical route, involving electro-oxidative decarboxylation and Kolbe coupling reactions. The new route is an example of the use of glutamic acid as
F R Johannsen et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 7(1), 33-40 (1986-07-01)
Acetonitrile (ACN), adiponitrile (ADN), and propionitrile (PN), were evaluated for embryotoxic and teratogenic potential in rats. Mated Sprague-Dawley rats were administered one of the three nitriles by gavage on gestation Days 6-19, inclusive. Daily dosage levels (mg/kg body wt) were:
Soo-Jin Yeom et al.
The Biochemical journal, 415(3), 401-407 (2008-04-17)
Nitrilase from Rhodococcus rhodochrous ATCC 33278 hydrolyses both aliphatic and aromatic nitriles. Replacing Tyr-142 in the wild-type enzyme with the aromatic amino acid phenylalanine did not alter specificity for either substrate. However, the mutants containing non-polar aliphatic amino acids (alanine
Electrolyte formulations based on dinitrile solvents for high voltage Li-ion batteries.
Duncan H, et al.
Journal of the Electrochemical Society, 160(6), A838-A848 (2013)
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