Skip to Content
Merck
CN

290637

cis-1,2-Dimethylcyclohexane

99%

Synonym(s):

cis-Hexahydro-o-xylene

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C6H10(CH3)2
CAS Number:
Molecular Weight:
112.21
EC Number:
218-621-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1900322
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

KVZJLSYJROEPSQ-OCAPTIKFSA-N

InChI

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

SMILES string

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

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.)

General description

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

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service