Skip to Content
MilliporeSigma
All Photos(1)

Documents

188220

Sigma-Aldrich

5-Phenyl-1-pentanol

98%

Synonym(s):

Benzenepentanol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5(CH2)5OH
CAS Number:
10521-91-2
Molecular Weight:
164.24
Beilstein/REAXYS Number:
1935233
EC Number:
234-064-8
MDL number:
MFCD00002979
UNSPSC Code:
12352100
PubChem Substance ID:
24851308
NACRES:
NA.22

assay

98%

form

liquid

refractive index

n20/D 1.516 (lit.)

bp

155 °C/20 mmHg (lit.)

density

0.975 g/mL at 25 °C (lit.)

SMILES string

OCCCCCc1ccccc1

InChI

1S/C11H16O/c12-10-6-2-5-9-11-7-3-1-4-8-11/h1,3-4,7-8,12H,2,5-6,9-10H2

InChI key

DPZMVZIQRMVBBW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

5-Phenyl-1-pentanol undergoes oxidation in the presence of ceric ammonium nitrate to yield 2-benzyltetrahydrofuran.

Application

5-Phenyl-1-pentanol was used in the synthesis of:
  • methoxy and fluorine analogs of N-(piperidinyl)-1-(2,4-dichlorophenyl)-4-methyl-5-(4-pentylphenyl)-1H-pyrazole-3-carboxamide (O-1302)
  • 2-[5-(4-iodophenyl)-pentyl]oxirane-2-carboxylic acid ethyl ester

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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

H G Abbas et al.
International journal of radiation applications and instrumentation. Part A, Applied radiation and isotopes, 42(1), 7-11 (1991-01-01)
A method is described for the synthesis, purification and radiolabelling of [123I/131I]2-[5-(4-iodophenyl)-pentyl]oxirane-2-carboxylic acid ethyl ester. For the synthesis of this new agent, 5-phenylpentyl bromide (1), synthesized by reacting 5-phenyl-1-pentanol with sodium bromide under acidic conditions, was converted to diethyl 5-phenylpentylmalonate
Shintaro Tobiishi et al.
Chemical & pharmaceutical bulletin, 55(8), 1213-1217 (2007-08-02)
Methoxy and fluorine analogs substituted on the terminal carbon of the pentyl chain of N-(piperidinyl)-1-(2,4-dichlorophenyl)-4-methyl-5-(4-pentylphenyl)-1H-pyrazole-3-carboxamide (O-1302) were synthesized in a multi-step process from 5-phenyl-1-pentanol, which was based on the 1,5-diarylpyrazole core template of N-(piperidinyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (SR141716) through condensation of the respective
Cyclic ether formation in oxidations of primary alcohols by cerium (IV). Reactions of 5-phenyl-1-pentanol, 4-phenyl-1-butanol, and 3-phenyl-1-propanol with ceric ammonium nitrate.
Doyle MP, et al.
The Journal of Organic Chemistry, 40(10), 1454-1456 (1975)
Hidetaka Nagatomo et al.
Bioscience, biotechnology, and biochemistry, 69(1), 128-136 (2005-01-25)
Hyperthermostable beta-glucosidase from Pyrococcus furiosus was enclosed in gelatin gel by cross-linking with transglutaminase. Gelatin-immobilized beta-glucosidase was considerably more thermostable than the native enzyme. Lyophilized immobilisate was stored at 90 degrees C for 1 month without loss of activity. The

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