Skip to Content
Merck
All Photos(2)

Documents

C27409

Sigma-Aldrich

4-Chlorobenzylamine

98%

Synonym(s):

(4-Chlorophenyl)methanamine, (4-Chlorophenyl)methylamine, (p-Aminomethyl)phenyl chloride, (p-Chlorophenyl)methylamine, 1-(4-Chlorophenyl)methanamine, 4-Chlorobenzenemethanamine, p-Chlorobenzenemethanamine, p-Chlorobenzylamine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ClC6H4CH2NH2
CAS Number:
Molecular Weight:
141.60
Beilstein:
507949
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.558 (lit.)

bp

215 °C (lit.)

density

1.164 g/mL at 25 °C (lit.)

SMILES string

NCc1ccc(Cl)cc1

InChI

1S/C7H8ClN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2

InChI key

YMVFJGSXZNNUDW-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °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

Stephen R Davies et al.
Drug testing and analysis, 11(2), 257-266 (2018-08-22)
Two human metabolites of the REV-ERB agonist SR9009, identified by researchers with an interest in sports doping control, have been synthesized and assessed for purity. The synthesis employed was a modification of published procedures for the parent SR9009, careful attention
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