38180
Diisobutylene
technical, ≥90% (3 parts 2,4,4-trimethyl-1-pentene + 1 part 2,4,4-trimethyl-2-pentene, GC)
동의어(들):
2,4,4-Trimethyl-1-pentene + 2,4,4-Trimethyl-2-pentene
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
(CH3)3CCH2C(CH3)=CH2+(CH3)3CCH=C(CH3)2
CAS Number:
Molecular Weight:
112.21
Beilstein:
1098309
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.21
추천 제품
grade
technical
Quality Level
분석
≥90% (3 parts 2,4,4-trimethyl-1-pentene + 1 part 2,4,4-trimethyl-2-pentene, GC)
refractive index
n20/D 1.411
bp
101-103 °C (lit.)
density
0.716 g/mL at 20 °C (lit.)
SMILES string
CC(=C)CC(C)(C)C
InChI
1S/C8H16/c1-7(2)6-8(3,4)5/h1,6H2,2-5H3
InChI key
FXNDIJDIPNCZQJ-UHFFFAOYSA-N
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일반 설명
Diisobutylene is an acyclic alkene. It is composed of a mixture of 2,4,4-trimethyl-1-pentene and 2,4,4- trimethyl-2-pentene (isomeric forms of diisobutylene). It is isostructural to to iso-octane. It can be synthesized from tertiary butyl alcohol.
애플리케이션
Diisobutylene, an alkene, may be used in the following studies:
- To compose alternalte diesel fuel.
- As fuel in single-cylinder engine; exhaust generated from combustion due to the burning of fuel has been reported to contain high concentrations of olefins.1
- Preparation of mono- and dialkylated diphenylamines.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - STOT SE 3
표적 기관
Central nervous system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
21.2 °F - closed cup
Flash Point (°C)
-6 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Alkylation of diphenylamine with α-methylstyrene and diisobutylene using acid-treated clay catalysts.
Chitnis SR and Sharma MM.
J. Catal., 160(1), 84-94 (1996)
The development of a detailed chemical kinetic mechanism for diisobutylene and comparison to shock tube ignition times.
Metcalfe WK, et al.
Proceedings of the Combustion Institute, 31(1), 377-384 (2007)
The isomers in ?diisobutylene?. II1.
Tongberg CO, et al.
Journal of the American Chemical Society, 54(9), 3706-3710 (1932)
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