M39407
Methylcyclopentane
97%
Synonym(s):
Methycyclopentane
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About This Item
Linear Formula:
C5H9CH3
CAS Number:
Molecular Weight:
84.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-503-2
Beilstein/REAXYS Number:
1900214
MDL number:
Assay:
97%
InChI key
GDOPTJXRTPNYNR-UHFFFAOYSA-N
InChI
1S/C6H12/c1-6-4-2-3-5-6/h6H,2-5H2,1H3
SMILES string
CC1CCCC1
vapor pressure
232.8 mmHg ( 37.7 °C)
assay
97%
autoignition temp.
624 °F
expl. lim.
8.35 %
refractive index
n20/D 1.409 (lit.)
bp
72 °C (lit.)
mp
−142 °C (lit.)
density
0.749 g/mL at 25 °C (lit.)
Quality Level
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Application
Methylcyclopentane can undergo ring opening or ring enlargement to yield various hydrocarbons including branched and unbranched hexanes, cyclohexane and benzene.
hcodes
signalword
Danger
Hazard Classifications
Asp. Tox. 1 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
1.4 °F
flash_point_c
-17 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Ring-opening reactions of methylcyclopentane over metal catalysts, M= Pt, Rh, Ir, and Pd: A mechanistic study from first-principles calculations.
Zhao, Zhi-Jian et al.
ACS Catalysis, 3(2), 196-205 (2013)
Effect of acidic properties of mesoporous zeolites supporting pt nanoparticles on hydrogenative conversion of methylcyclopentane.
Na, Kyungsu et al.
Journal of the American Chemical Society, 136(49), 17207-17212 (2014)
Size and shape dependence on Pt nanoparticles for the methylcyclopentane/hydrogen ring opening/ring enlargement reaction.
Alayoglu, S et al.
Catalysis Letters, 141(7), 914-924 (2011)
Haijing Wang et al.
Journal of chromatographic science, 53(5), 647-654 (2014-09-17)
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