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196169

3-Methylcyclopentanol, mixture of isomers

99%

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About This Item

Linear Formula:
CH3C5H8OH
CAS Number:
18729-48-1
Molecular Weight:
100.16
NACRES:
NA.22
PubChem Substance ID:
24851739
UNSPSC Code:
12352100
EC Number:
242-540-1
MDL number:
MFCD00001368
Assay:
99%
Form:
liquid
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assay

99%

form

liquid

refractive index

n20/D 1.446 (lit.)

bp

149-150 °C (lit.)

density

0.91 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CC1CCC(O)C1

InChI

1S/C6H12O/c1-5-2-3-6(7)4-5/h5-7H,2-4H2,1H3

InChI key

VEALHWXMCIRWGC-UHFFFAOYSA-N

Application

3-Methylcyclopentanol has been used in the synthesis of pentacycloalkoxy-substituted phosphazenes and 3-methyl cyclopentylbromide.

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

131.0 °F - closed cup

flash_point_c

55 °C - closed cup

ppe

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
MKBK2942V
41496LJV
41496LJ
19016DQ
16618MU

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A Synthetic Procedure for Secondary Bromides from Alcohols.
Jenkins GL and Kellett Jr JC.
The Journal of Organic Chemistry, 27(2), 624-625 (1962)
The synthesis and characterization of cycloalkoxy-linear phosphazenes.
Ozturk AI, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 178(10), 2097-2105 (2003)
Mireia Oromí-Farrús et al.
Journal of analytical methods in chemistry, 2012, 452949-452949 (2012-06-01)
The use of iodine as a catalyst and either acetic or trifluoroacetic acid as a derivatizing reagent for determining the enantiomeric composition of acyclic and cyclic aliphatic chiral alcohols was investigated. Optimal conditions were selected according to the molar ratio

Global Trade Item Number

SKUGTIN
196169-5G04061837006616