Skip to Content
Merck
All Photos(1)

Documents

Safety Information

C27115

Sigma-Aldrich

4-Chlorobenzyl alcohol

99%

Synonym(s):

1-Chloro-4-(hydroxymethyl)benzene, 4-Chlorobenzenemethanol, 4-Chlorophenylmethanol, p-Chlorobenzyl alcohol, p-Chlorotoluol

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

About This Item

Linear Formula:
ClC6H4CH2OH
CAS Number:
873-76-7
Molecular Weight:
142.58
Beilstein:
636502
EC Number:
212-852-2
MDL number:
MFCD00004652
UNSPSC Code:
12352100
PubChem Substance ID:
24892520
NACRES:
NA.22

Assay

99%

form

crystals

bp

234 °C (lit.)

mp

68-71 °C (lit.)

SMILES string

OCc1ccc(Cl)cc1

InChI

1S/C7H7ClO/c8-7-3-1-6(5-9)2-4-7/h1-4,9H,5H2

InChI key

PTHGDVCPCZKZKR-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Reagent for carboxyl group protection.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

C27115-25G:
C27115-VAR:
C27115-100G:
C27115-BULK:

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

Customers Also Viewed

Slide 1 of 1

1 of 1

4-(Chloromethyl)benzyl alcohol 99%

Sigma-Aldrich

526126

4-(Chloromethyl)benzyl alcohol

Mario Silva et al.
Journal of chromatography. A, 1629, 461508-461508 (2020-08-29)
In the present document, we report the development of an analytical method consisting of a sequential direct-immersion/headspace solid-phase microextraction (DI-HS-SPME) followed by gas-phase chromatography and tandem mass spectrometry (GC-MS/MS) for simultaneous analysis of 4-chlorobenzyl alcohol, 2,6-dichlorobenzyl alcohol, 4-methoxybenzyl alcohol, 3,4-dimethoxybenzyl
Kenji Matsuno et al.
Bioorganic & medicinal chemistry letters, 20(17), 5126-5129 (2010-08-07)
S-benzylisothiourea 3a was discovered by its ability to inhibit indoleamine-2,3-dioxygenase (IDO) in our screening program. Subsequent optimization of the initial hit 3a lead to the identification of sub-muM inhibitors 3r and 10h, both of which suppressed kynurenine production in A431

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