Skip to Content
Merck

Key Documents

View All Documentation

Skip To

187828

Sigma-Aldrich

2-tert-Butylcyclohexanol, mixture of isomers

99%

Sign Into View Organizational & Contract Pricing

Select a Size

Change View
100 G
RM 214.00

About This Item

Linear Formula:
(CH3)3CC6H10OH
CAS Number:
13491-79-7
Molecular Weight:
156.27
EC Number:
236-806-6
MDL number:
MFCD00001472
UNSPSC Code:
12352100
PubChem Substance ID:
24851286
NACRES:
NA.22

RM 214.00

Check Cart for Availability
Request a Bulk Order
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

100

Assay

99%

form

solid

mp

43-46 °C (lit.)

density

0.902 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CC(C)(C)C1CCCCC1O

InChI

1S/C10H20O/c1-10(2,3)8-6-4-5-7-9(8)11/h8-9,11H,4-7H2,1-3H3

InChI key

DLTWBMHADAJAAZ-UHFFFAOYSA-N

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
146641369500218286
2-tert-Butylcyclohexanol, mixture of isomers 99%

187828

2-tert-Butylcyclohexanol, mixture of isomers

3-Nitro-2-butanol, mixture of isomers 98%

146641

3-Nitro-2-butanol, mixture of isomers

4,4′-Methylenebis(2-methylcyclohexylamine), mixture of isomers 99%

369500

4,4′-Methylenebis(2-methylcyclohexylamine), mixture of isomers

(+)-Dihydrocarvone, mixture of isomers 98%

218286

(+)-Dihydrocarvone, mixture of isomers

assay

99%

assay

98%

assay

99%

assay

98%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

solid

form

liquid

form

liquid

form

liquid

mp

43-46 °C (lit.)

mp

-

mp

-

mp

-

density

0.902 g/mL at 25 °C (lit.)

density

1.1 g/mL at 25 °C (lit.)

density

0.94 g/mL at 25 °C (lit.)

density

0.929 g/mL at 25 °C (lit.)

functional group

hydroxyl

functional group

amine, hydroxyl, nitro

functional group

-

functional group

ketone

General description

2-tert-Butylcyclohexanol is the major metabolite of (+/-)-2-tert-butylcyclohexanone[1].

Application

2-tert-Butylcyclohexanol was used in the synthesis of 2-tert-butylcyclohexyl methacrylate via reaction with methacryloyl chloride in the presence of triethylamine[2].

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

174.2 °F - closed cup

Flash Point(C)

79 °C - closed cup

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    03427MR
    08819MS
    04431CZ
    26073

    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.

    Search for a COA

    Already Own This Product?

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

    Visit the Document Library

    K L Cheo et al.
    The Biochemical journal, 104(1), 198-204 (1967-07-01)
    1. (+/-)-2-, (+/-)-3- and 4-tert.-Butylcyclohexanone are reduced in the rabbit to secondary alcohols, which are excreted extensively conjugated with glucuronic acid. 2. The major metabolite of (+/-)-2-tert.-butylcyclohexanone is (+)-cis-2-tert.-butylcyclohexanol, which has been isolated from the urine as [(+)-cis-2-tert.-butylcyclohexyl beta-d-glucosid]uronic acid.
    Radical polymerization behavior of 2-tert-butylcyclohexyl methacrylate.
    Matsumoto A and Mizuta K.
    Polym. Bull., 33(2), 141-148 (1994)

    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