Skip to Content
Merck
All Photos(1)

Documents

470171

Sigma-Aldrich

3-Methyl-1-phenyl-3-pentanol

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5CH2CH2C(CH3)(C2H5)OH
CAS Number:
Molecular Weight:
178.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

refractive index

n20/D 1.511 (lit.)

bp

112-112.5 °C/0.8 mmHg (lit.)

density

0.938 g/mL at 25 °C (lit.)

SMILES string

CCC(C)(O)CCc1ccccc1

InChI

1S/C12H18O/c1-3-12(2,13)10-9-11-7-5-4-6-8-11/h4-8,13H,3,9-10H2,1-2H3

InChI key

AEJRTNBCFUOSEM-UHFFFAOYSA-N

General description

3-Methyl-1-phenyl-3-pentanol is a tertiary alcohol and belongs to the fragrance structural group Aryl Alkyl Alcohols. Sulfuric acid catalyzed cyclization of 3-methyl-1-phenyl-3-pentanol has been proposed.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °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’.

Already Own This Product?

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

Visit the Document Library

J Scognamiglio et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S168-S172 (2011-10-29)
A toxicologic and dermatologic review of 1-phenyl-3-methyl-3-pentanol when used as a fragrance ingredient is presented. 1-Phenyl-3-methyl-3-pentanol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a tertiary alcohol. The AAAs are a structurally diverse class of
Friedel-Crafts cyclialkylations of certain mono-and diphenyl-substituted alcohols and alkyl chlorides.
Khalaf AA and Roberts RM.
The Journal of Organic Chemistry, 37(26), 4227-4235 (1972)

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