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Merck

153613

Sigma-Aldrich

Pentamethylbenzene

98%

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About This Item

Fórmula lineal:
C6H(CH3)5
Número de CAS:
Peso molecular:
148.24
Beilstein/REAXYS Number:
1905349
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

form

solid

bp

231 °C (lit.)

mp

49-51 °C (lit.)

density

0.917 g/mL at 25 °C (lit.)

SMILES string

Cc1cc(C)c(C)c(C)c1C

InChI

1S/C11H16/c1-7-6-8(2)10(4)11(5)9(7)3/h6H,1-5H3

InChI key

BEZDDPMMPIDMGJ-UHFFFAOYSA-N

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Categorías relacionadas

Application

Pentamethylbenzene was used to prepare a mixture of nitropentamethylbenzene and 2,3,4,5-tetramethylbenzyl nitrate. It was also used to prepare propene.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

WGK 3

flash_point_f

195.8 °F - closed cup

flash_point_c

91 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Anomalous Products Obtained by Nitration of Pentamethylbenzene, Pentaethylbenzene, and Some Mixed Penta-alkylbenzenes.
Suzuki H and Nakamura K.
Bulletin of the Chemical Society of Japan, 43(2), 473-473 (1970)
Yingxin Sun et al.
Journal of molecular modeling, 19(12), 5407-5422 (2013-11-07)
Two-layer ONIOM calculations have been carried out to study methanol to propene (MTP) conversion reactions catalyzed by H-beta zeolite. On the basis of the so-called side-chain hydrocarbon pool (HCP) mechanism, this work proposes the complete catalytic cycle pathway for the
Xinghui Qiu et al.
Journal of economic entomology, 96(4), 1283-1289 (2003-09-25)
Differences in the microsomal P450 monooxygenase system and its inducibility by pentamethylbenzene (PMB) and naphathalene (NA) were investigated in midgut and fatbody tissues of the cotton bollworm, Helicoverpa armigera (Boddie), larvae. Orthogonal array design was used to establish the optimal
Induction of hepatic microsomal cytochrome P-450 and associated monooxygenases by pentamethylbenzene in the rat.
M S Denison et al.
Biochemical pharmacology, 32(17), 2610-2611 (1983-09-01)
B J Cochrane et al.
Biochemical pharmacology, 35(10), 1679-1684 (1986-05-15)
The enzyme glutathione-S-transferase, which plays a crucial role in xenobiotic detoxification, was investigated in Drosophila melanogaster. Based upon examination of substrate specificities and pH optima, it was observed that the enzyme in Drosophila is considerably more restricted in its activities

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