Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

427462

Sigma-Aldrich

5-Benzyloxy-1-pentanol

95%

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

About This Item

Linear Formula:
C6H5CH2O(CH2)5OH
CAS Number:
4541-15-5
Molecular Weight:
194.27
MDL number:
MFCD00216583
UNSPSC Code:
12352100
PubChem Substance ID:
24866761
NACRES:
NA.22

Assay

95%

refractive index

n20/D 1.505 (lit.)

bp

140 °C/0.4 mmHg (lit.)

density

1.008 g/mL at 25 °C (lit.)

functional group

ether
hydroxyl
phenyl

SMILES string

OCCCCCOCc1ccccc1

InChI

1S/C12H18O2/c13-9-5-2-6-10-14-11-12-7-3-1-4-8-12/h1,3-4,7-8,13H,2,5-6,9-11H2

InChI key

RZVDPWSEPVHOPU-UHFFFAOYSA-N

General description

5-Benzyloxy-1-pentanol (5-(benzyloxy)pentan-1-ol) has been synthesized by reacting pentane-1,5-diol with benzyl chloride. Its enthalpy of vaporization at boiling point has been determined.

Application

5-Benzyloxy-1-pentanol (5-(benzyloxy)pentan-1-ol) may be used as a starting material in the synthesis of 5-benzyloxypentanal and (±)tanikolide.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
04329HE
13329PC
12603PI
19306DU
13812CO

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

Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 514-514 (2008)
Total synthesis of (?) tanikolide.
Zhang R, et al.
Synthetic Communications, 32(14), 2187-2194 (2002)
Ana R Hornillo-Araujo et al.
Organic & biomolecular chemistry, 4(9), 1723-1729 (2006-04-25)
The syntheses of novel tricyclic pyrrolo[2,3-d]pyrimidine analogues of S6-methylthioguanine are described. The crystal structures and pKa values of these and related O6-methylguanine analogues are reported. All compounds display higher pKa values than O6-methylguanine with the sulfur-containing analogues being the more

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