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4-chlorobenzeneethanamine

Names

[ CAS No. ]:
156-41-2

[ Name ]:
4-chlorobenzeneethanamine

[Synonym ]:
4-chlorobenzeneethanamine
1-Amino-2-(4-chlorophenyl)ethane
2-(4-Chlorophenyl)ethylaMine
EINECS 205-853-4
MFCD00008191
2-(p-Chlorophenyl)-ethylamine
Benzeneethanamine, 4-chloro-
2-(4-Chlorophenyl)ethanamine
2-(p-Chlorophenyl)ethylamine
4-Chlorophenethyl amine

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
233.4±15.0 °C at 760 mmHg

[ Molecular Formula ]:
C8H10ClN

[ Molecular Weight ]:
155.625

[ Flash Point ]:
106.1±0.0 °C

[ Exact Mass ]:
155.050171

[ PSA ]:
26.02000

[ LogP ]:
2.05

[ Vapour Pressure ]:
0.1±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.555

[ Storage condition ]:
Store Cold

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
2735.0

[ WGK Germany ]:
3

[ HS Code ]:
2921499090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2921499090

[ Summary ]:
2921499090 other aromatic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Dopamine beta-hydroxylase: activity and inhibition in the presence of beta-substituted phenethylamines.

Biochemistry 21(1) , 67-75, (1982)

Use of alternate substrates to probe the order of substrate addition to dopamine beta-hydroxylase.

Arch. Biochem. Biophys. 249(1) , 70-5, (1986)

In order to determine the order of substrate binding to dopamine beta-hydroxylase during catalysis, the effect of alternate substrates upon kinetic parameters was examined. The V/K value for ascorbate...

Comparative effects of various serotonin releasing agents in mice.

Biochem. Pharmacol. 29(23) , 3163-7, (1980)


More Articles


Related Compounds