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290637

Sigma-Aldrich

cis-1,2-Dimethylcyclohexane

99%

Synonym(s):

cis-Hexahydro-o-xylene

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About This Item

Linear Formula:
C6H10(CH3)2
CAS Number:
2207-01-4
Molecular Weight:
112.21
Beilstein:
1900322
EC Number:
218-621-2
MDL number:
MFCD00063621
UNSPSC Code:
12352100
PubChem Substance ID:
24857480
Pricing and availability is not currently available.

vapor pressure

28 mmHg ( 37.7 °C)

Assay

99%

autoignition temp.

579 °F

refractive index

n20/D 1.436 (lit.)

bp

129-130 °C (lit.)

density

0.796 g/mL at 25 °C (lit.)

SMILES string

C[C@@H]1CCCC[C@@H]1C

InChI

1S/C8H16/c1-7-5-3-4-6-8(7)2/h7-8H,3-6H2,1-2H3/t7-,8+

InChI key

KVZJLSYJROEPSQ-OCAPTIKFSA-N

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General description

cis-1,2-Dimethylcyclohexane has been oxidized by O2 in the presence of iron(II)-bispidine complexes[1]. It has been known to form plastic crystals which can be supercooled to show a glass transition at a temperature Tg[2].

Signal Word

Danger

Hazard Statements

H225,H304,H411

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBD5083V
07702JH
06130EH
16303EF
13221EF

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Study of the nature of glass transitions in the plastic crystalline phases of cyclo-octanol, cycloheptanol, cyanoadamantane and cis-1, 2-dimethylcyclohexane.
Tyagi M and Murthy SSN.
J. Chem. Phys. , 114(8), 3640-3652 (2001)
Peter Comba et al.
Chemical communications (Cambridge, England), 50(4), 412-414 (2013-11-20)
Organic substrates (specifically cis-1,2-dimethylcyclohexane, DMCH) are oxidized by O2 in the presence of iron(II)-bispidine complexes. It is shown that this oxidation reaction is not based on O2 activation by the nonheme iron catalysts as in Nature but due to a
Frank-Dieter Kopinke et al.
Environmental science & technology, 45(23), 10013-10019 (2011-11-01)
This study presents a new experimental technique for measuring rates of desorption of organic compounds from dissolved organic matter (DOM) such as humic substances. The method is based on a fast solid-phase extraction of the freely dissolved fraction of a
Acute toxicities to larval rainbow trout of representative compounds detected in Great Lakes fish.
C C Edsall
Bulletin of environmental contamination and toxicology, 46(2), 173-178 (1991-02-01)

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