L-1-Phenylethylamine

Suppliers

Names

[ Name ]:
L-1-Phenylethylamine

[Synonym ]:
(S)-(−)-1-Phenylethylamine
(S)-(-)-α-Methylbenzylamine
(1R)-1-Phenylethanamine
(s)-benzenemethanamin
L-PHENYLETHYLAMINE
(S)-1-phenyl-ethylamine
N-Ethyl-N-phenylamine
L-Phenethylamine
(R)-α-Methylbenzenemethanamine
(1R)-1-Phenylethylamine
(S)-(−)-α-Methylbenzylamine
S(-)PHENYLETHYLAMINE
N-Ethylaniline
ANILINE,N-ETHYL
R-(+)-α-Phenylethylamine
N-Ethylbenzenamine
L(-)-alpha-Methylbenzylamine
benzenemethanamine, a-methyl-, (aR)-
(1S)-1-PHENYLETHYLAMINE
EINECS 220-098-0
1-Phenylethylamine
N-Ethylaniline [UN2272] [Poison]
(S)-1-PHENYLETHANAMINE
Benzenemethanamine, α-methyl-, (αR)-
S-(-)-α-phenylethylamine
(S)-(-)-1-Phenylethylamine
(1R)-(+)-1-Phenylethylamine
N-ethylbenzeneamine
aniline, N-ethyl-
Benzenamine, N-ethyl-
p-Ethylaminobenzene
N-Ethylaminobenzene
Benzenemethanamine, α-methyl-, (R)-
(-)-PEA
(S)-(-)-Alpha-Methylbenzylamine
(R)-(+)-α-Methylbenzylamine
(R)-1-phenylethylamine
(R)-1-phenylethanamine
(+)-α-PHENYLETHYLAMINE
MFCD00064406
(+)-α-Methylbenzylamine
n-Ethyl aniline
(S)-(-)-1-METHYLBENZYLAMINE
L-1-Phenylethylamine

Chemical & Physical Properties

[ Density]:
0.94

[ Boiling Point ]:
187-189 ºC

[ Melting Point ]:
-10ºC

[ Molecular Formula ]:
C₈H₁₁N

[ Molecular Weight ]:
121.180

[ Flash Point ]:
79 ºC

[ Exact Mass ]:
121.089149

[ PSA ]:
26.02000

[ LogP ]:
1.44

[ Vapour Pressure ]:
0.8±0.3 mmHg at 25°C

[ Index of Refraction ]:
1.533

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302-H311-H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

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

[ Hazard Codes ]:
C:Corrosive

[ Risk Phrases ]:
R21/22;R35

[ Safety Phrases ]:
S26-S28-S36/37/39-S45

[ RIDADR ]:
UN 2735

[ WGK Germany ]:
1

[ RTECS ]:
DP5775000

[ Packaging Group ]:
III

[ HS Code ]:
29214980

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

N-[tert-butyl-(S)-sulfinyl]-methylphenylketimine
Acetophenone
N-[(1S)-1-phenylethan-1-yl]-4-methylbenzenesulfonamide
(s)-(-)-n-acetyl-1-methylbenzylamine

DownStream

4-(Trifluoromethyl)benzylamine
Acetophenone
ethylbenzylamine
(R)-(+)-N-acetyl-1-methylbenzylamine
(S)-(+)-2-METHYLGLUTARICACID
(r)-(-)-2-hydroxy-2-phenylpropionic acid
(S)-atrolactic acid (S)-(-)-α-methylbenzylamine salt
Methylbenzylalcohol
Benzylamine
(±)-1-phenylethanol

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

Interactions of an asymmetric amine with a non-C2 symmetric Cu-salen complex: an EPR/ENDOR and HYSCORE investigation.

Phys. Chem. Chem. Phys. 13(45) , 20427-34, (2011)

Single enantiomers of R-/S-methylbenzylamine (MBA) were found to selectively form adducts with the chiral non-C(2) symmetric Cu-salen complex N-(3,5-di-tert-butylsalicylidene)-N'-(salicylidene)-cycloh...

Synthesis, Crystal Structure, Absolute Configuration and Antitumor Activity of the Enantiomers of 5-Bromo-2-chloro-N-(1-phenylethyl)pyridine-3-sulfonamide.

Molecules 20 , 20926-38, (2015)

Pyridinesulfonamide is an important fragment which has a wide range of applications in novel drugs. R- and S-isomers of 5-bromo-2-chloro-N-(1-phenylethyl)pyridine-3-sulfonamide have been synthesized, ...

Enantioselective nanofiber-spinning of chiral calixarene receptor with guest.

Chem. Commun. (Camb.) (32) , 3398-400, (2007)

Chiral para-tert-butylcalix[4]arene bearing (S)-alpha-methylbenzylamine groups at lower rim only self-assembles with one of two enantiomers of 2,3-dibenzoyltartaric acid into coiled nanofibers and the...

(1S)-pyruvoyl-1-phenylethylamine
S-(-)-N-Benzyl-1-phenylethylamine
(S)-(-)-N-BENZYL-1-PHENYLETHYLAMINE
(R)-N-BOC-N-methyl-1-phenylethylamine
(1S)-N-Isopropyl-N-methyl-1-phenylethylamine
(r)-(+)-n-allyl-1-phenylethylamine hydrochloride
3-[(Tert-butyldimethylsilyl)oxy]-2-[1-(2-methylpropyl)piperidin-4-yl]propan-1-ol
2-(Azetidin-3-yl)-3-[(tert-butyldimethylsilyl)oxy]propan-1-ol
3-{1-[(Tert-butyldimethylsilyl)oxy]-3-hydroxypropan-2-yl}-8lambda6-thiabicyclo[3.2.1]octane-8,8-dione
5-(1-Ethylpiperidin-4-yl)-2-methyl-1,3,2lambda5-dioxaphosphinane-2-thione
5-{1,4-Dioxaspiro[4.5]decan-8-yl}-2-methyl-1,3,2lambda5-dioxaphosphinane-2-thione
5-(4,4-Dimethylcyclohexyl)-2-methyl-1,3,2lambda5-dioxaphosphinane-2-thione
4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-{[(6-oxopiperidin-2-yl)methyl]carbamoyl}butanoic acid
2-[(1-Hydroxypent-4-yn-2-yl)amino]-1,3-thiazole-4-carboxylic acid
1-{1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]spiro[2.3]hexane-1-carbonyl}azetidine-3-carboxylic acid
2-[2-({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]spiro[2.3]hexan-1-yl}formamido)ethoxy]acetic acid

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.