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线性分子式:
(CH3)3CCH2C(CH3)=CH2
化学文摘社编号:
分子量:
112.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-486-4
Beilstein/REAXYS Number:
1098309
MDL number:
Assay:
96%
Form:
liquid
产品名称
2,4,4-三甲基-1-戊烯, 96%
InChI key
FXNDIJDIPNCZQJ-UHFFFAOYSA-N
InChI
1S/C8H16/c1-7(2)6-8(3,4)5/h1,6H2,2-5H3
SMILES string
CC(=C)CC(C)(C)C
vapor density
>3.8 (vs air)
vapor pressure
83 mmHg ( 37.7 °C)
assay
96%
form
liquid
autoignition temp.
736 °F
expl. lim.
4.8 %
refractive index
n20/D 1.408 (lit.)
bp
101-102 °C (lit.)
density
0.708 g/mL at 25 °C (lit.)
Quality Level
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General description
2,4,4-Trimethyl-1-pentene is a α-alkene. It is the main dimeric product of isobutene. Ozonolysis of 2,4,4-trimethyl-1-pentene has been investigated in a flow reactor under pseudo-first-order conditions. Hydrocracking (HCG) of 2,4,4-trimethyl-1-pentene has been employed as a model test reaction to investigate the catalytic functionalities of sulfided CoMo catalysts. Liquid phase oxidation of 2,4,4-trimethyl-1-pentene with molecular xygen afforded epoxides and hydrogen peroxides.
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
25.0 °F - closed cup
flash_point_c
-3.9 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
The origin of epoxides in the liquid phase oxidation of olefins with molecular oxygen.
Brill WF.
Journal of the American Chemical Society, 85(2), 141-145 (1963)
Catalytic functionalities of supported sulfides: I. Effect of support and additives on the CoMo catalyst.
Muralidhar G, et al.
J. Catal., 85(1), 44-52 (1984)
Reaction equilibrium in the isomerization of 2, 4, 4-trimethyl pentenes.
Karinen RS, et al.
Industrial & Engineering Chemistry Research, 40(4), 1011-1015 (2001)
Diisobutylene.
American Industrial Hygiene Association journal, 43(1), B83-B84 (1982-01-01)
Marius Duncianu et al.
The journal of physical chemistry. A, 116(24), 6169-6179 (2012-01-25)
A new flow reactor has been developed to study ozonolysis reactions at ambient pressure and room temperature (297 ± 2 K). The reaction kinetics of O(3) with 4-methyl-1-pentene (4M1P), 2-methyl-2-pentene (2M2P), 2,4,4-trimethyl-1-pentene (tM1P), 2,4,4-trimethyl-2-pentene (tM2P) and α-pinene have been investigated
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