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104191

Sigma-Aldrich

trans-4-Methylcyclohexanol

97%

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About This Item

Linear Formula:
CH3C6H10OH
CAS Number:
7731-29-5
Molecular Weight:
114.19
EC Number:
231-790-7
MDL number:
MFCD00064171
UNSPSC Code:
12352100
PubChem Substance ID:
24846430
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.455 (lit.)

bp

173-175 °C (lit.)

density

0.912 g/mL at 25 °C (lit.)

SMILES string

C[C@@H]1CC[C@@H](O)CC1

InChI

1S/C7H14O/c1-6-2-4-7(8)5-3-6/h6-8H,2-5H2,1H3/t6-,7-

InChI key

MQWCXKGKQLNYQG-LJGSYFOKSA-N

Related Categories

General description

trans-4-Methylcyclohexanol is an active Aedes triseriatus oviposition attractant.

Application

trans-4-Methylcyclohexanol was used to prepare 4-methylcyclohexyl nitrite to study the laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals.

Biochem/physiol Actions

trans-4-Methylcyclohexanol is the major metabolite formed by biological regioselective reduction of 4-methylcyclohexanone by Glomerella cingulata.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

158.0 °F - closed cup

Flash Point(C)

70 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Biological enantioselective reduction of methylcyclohexanones by Glomerella cingulata.
Miyazawa M, et al.
Journal of Chemical Technology and Biotechnology, 65(2), 171-175 (1996)
Lei Zhang et al.
The journal of physical chemistry. A, 109(41), 9232-9240 (2006-07-13)
The laser-induced fluorescence (LIF) excitation spectra of the 4-methylcyclohexoxy and d11-cyclohexoxy radicals have been measured for the first time. LIF intensity was used as a probe in direct kinetic studies of the reaction of O(2) with trans-4-methylcyclohexoxy and d11-cyclohexoxy radicals
M Kutsukake et al.
Gene, 245(1), 31-42 (2000-03-14)
We characterized molecular profiles of a new olfactory mutant line, honoka (hono), which was found among 500 viable P-element insertion lines screened first by 5-bromo-4-chloro-3-indrolyl-beta-D-galactopyranoside (X-gal) staining on the third segment of the antenna, and then by behavioral assays to
J R Linley
Medical and veterinary entomology, 3(4), 347-352 (1989-10-01)
Laboratory experiments tested the effects of p-cresol or 4-methylcyclohexanol at concentrations of 1, 10 and 50 ppm, on oviposition by the mosquitoes Toxorhynchites brevipalpis Theobald, Tx. amboinensis (Doleschall) and Tx. splendens (Wiedemann). A 5 + 5 ppm mixture of the
Jianzeng Guo et al.
Science (New York, N.Y.), 309(5732), 307-310 (2005-07-09)
Different modalities of sensation interact in a synergistic or antagonistic manner during sensory perception, but whether there is also interaction during memory acquisition is largely unknown. In Drosophila reinforcement learning, we found that conditioning with concurrent visual and olfactory cues
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