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(R)-(+)-1-(4-Methylphenyl)ethylamine

CAS No.
4187-38-6
Chemical Name:
(R)-(+)-1-(4-Methylphenyl)ethylamine
Synonyms
Tolylethylamine;(R)-1-P-TOLYLETHANAMINE;Methyl phenyl-ethylamine;(+)-p,α-Dimethylbenzylamine;alpha,4-dimethylbenzylamine;(R)-1-(p-tolyl)ethan-1-amine;(R)-(+)-1-(P-TOLYL)ETHYLAMINE;(R)-(+)-A-(P-TOLYL)ETHYLAMINE;(R)-(+)-4-(1-AMINOETHYL)TOLUENE;(R)-alpha,p-Dimethylbenzylamine
CBNumber:
CB9311444
Molecular Formula:
C9H13N
Molecular Weight:
135.21
MDL Number:
MFCD00145202
MOL File:
4187-38-6.mol
MSDS File:
SDS
Last updated:2023-11-20 10:14:03

(R)-(+)-1-(4-Methylphenyl)ethylamine Properties

Melting point <-20°C
Boiling point 205 °C (lit.)
alpha 37 º (NEAT)
Density 0.919 g/mL at 25 °C (lit.)
refractive index n20/D 1.521(lit.)
Flash point 180 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka 9.20±0.10(Predicted)
Specific Gravity 0.919
optical activity [α]20/D +37°, neat
Sensitive Air Sensitive
BRN 3195425
CAS DataBase Reference 4187-38-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS05,GHS07
Signal word  Danger
Hazard statements  H302+H312+H332-H314
Precautionary statements  P261-P280-P301+P312-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  C
Risk Statements  20/21/22-34
Safety Statements  16-26-27-36/37/39-45
RIDADR  UN 2619 8/PG 2
WGK Germany  3
HazardClass  8
PackingGroup  III
HS Code  2921490090
NFPA 704
2
3 0

(R)-(+)-1-(4-Methylphenyl)ethylamine price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 726664 (R)-(+)-α,4-Dimethylbenzylamine ChiPros 4187-38-6 5g $104 2024-03-01 Buy
Sigma-Aldrich 405248 (R)-(+)-α,4-Dimethylbenzylamine 98% 4187-38-6 1g $122 2023-06-20 Buy
TCI Chemical T1380 (R)-(+)-1-(p-Tolyl)ethylamine >98.0%(GC) 4187-38-6 1mL $99 2021-12-16 Buy
Alfa Aesar L16328 (R)-(+)-1-(4-Methylphenyl)ethylamine, ChiPros 98+% ee 98% 4187-38-6 5g $71 2021-12-16 Buy
Alfa Aesar L16328 (R)-(+)-1-(4-Methylphenyl)ethylamine, ChiPros 98+% ee 98% 4187-38-6 1g $34.9 2021-12-16 Buy
Product number Packaging Price Buy
726664 5g $104 Buy
405248 1g $122 Buy
T1380 1mL $99 Buy
L16328 5g $71 Buy
L16328 1g $34.9 Buy

(R)-(+)-1-(4-Methylphenyl)ethylamine Chemical Properties,Uses,Production

Chemical Properties

Colorless to light yellow liquid

Uses

(R)-(+)-α,4-Dimethylbenzylamine can be used as a chiral salt of keto acid, employed in the solid-state photolysis studies of α-mesitylacetophenone derivatives.

Application

(R)-(+)-α,4-Dimethylbenzylamine reacts with 1,5-difluoro-2,4-dinitrobenzene (DFDNB) to form a chiral derivative reagent(CDR) via substitution of one fluorine atom.

General Description

(R)-(+)-α,4-Dimethylbenzylamine is a chiral amine.

Synthesis

(R)-(+)-1-(4-methylphenyl)ethylamine was synthesized via a series of chemical reactions with (R)-N-[1-(4-methylphenyl)ethyl]acetamide. The steps are as follows:
1 g of the compound obtained in the previous stage will be used. 2 g of n-butanol was added, 0.63 g of potassium hydroxide was added, and the temperature was raised to 100 ° C. After 24 hours of heat preservation, cool down to 10 to 20 ℃. After adding water and stirring for 0.5 hours, the mixture was allowed to stand for separation, and the organic layer was concentrated to n-butanol, and then subjected to vacuum distillation (80-100 ℃ packed column) to obtain (R)-1-(4-methylphenyl)ethylamine 0.63 g. The yield was 82%, the HPLC purity was 96.3%, and the enantiomer was 0.8%.
(R)-(+)-1-(4-Methylphenyl)ethylamine synthesis

structure and hydrogen bonding

(R)-(+)-1-(4-Methylphenyl)ethylamine is a chiral molecule studied in the context of crystallographic analysis and optimization. Through X-ray diffraction analysis, the crystal structure of (R)-(+)-1-(4-Methylphenyl)ethylamine was determined, revealing the presence of a significant hydrogen bond between the amine group and one of the carbonyl groups. This hydrogen bond plays a crucial role in stabilizing the (R)-(+)-1-(4-Methylphenyl)ethylamine molecule, which is a recurring pattern observed in structurally similar compounds. Furthermore, the (S)-(+)-enantiomer of (R)-(+)-1-(4-Methylphenyl)ethylamine was synthesized using an enantiopure precursor, establishing an efficient method to obtain this desired form of the molecule.

(R)-(+)-1-(4-Methylphenyl)ethylamine Preparation Products And Raw materials

Raw materials

Preparation Products

(R)-(+)-1-(4-Methylphenyl)ethylamine Suppliers

Global( 146)Suppliers
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Shanghai Jinli Pharmaceutical Co.,Ltd
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+86-852-30606658 market18@leapchem.com China 43348 58

View Lastest Price from (R)-(+)-1-(4-Methylphenyl)ethylamine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
(R)-(+)-1-(4-Methylphenyl)ethylamine pictures 2020-01-13 (R)-(+)-1-(4-Methylphenyl)ethylamine
4187-38-6
US $3.00 / KG 1KG 98% 200KG Career Henan Chemical Co
(R)-alpha,p-Dimethylbenzylamine Tolylethylamine Methyl phenyl-ethylamine (R)-(+)-4-(1-AMINOETHYL)TOLUENE (R)-4-METHYL-ALPHA-METHYLBENZYLAMINE (R)-(+)-ALPHA,4-DIMETHYLBENZYLAMINE (R)-(+)-A-(P-TOLYL)ETHYLAMINE (R)-(+)-1-(4-METHYLPHENYL)ETHYLAMINE (R)-1-(4-METHYLPHENYL)ETHYLAMINE (R)-1-P-TOLYLETHANAMINE (R)-(+)-1-(P-TOLYL)ETHYLAMINE Benzenemethanamine, .alpha.,4-dimethyl-, (.alpha.R)- (R)-1-(4-METHYLPHENYL)ETHYLAMINE-HCl (+)-p,α-Dimethylbenzylamine (αR)-α,4-Dimethylbenzenemethanamine [R,(+)]-p,α-Dimethylbenzylamine (R)-(+)-ALPHA,4-DIMETHYLBENZYLAMINE, 98+ % (98% EE/GLC) (R)-(+)-α,4-DIMETHYLBENZYLAMINE (R)-(+)-1-(4-METHYLPHENYL)ETHYLAMINE , EE 98% (R)-(+)-1-(P-TOLYL)ETHYLAMINE 98+% (R)-(+)-1-(4-METHYLPHENYL)ETHYLAMINE, CHIPROS 98+%, EE 98% Benzenemethanamine, α,4-dimethyl-, (αR)- alpha,4-dimethylbenzylamine (R)-(+)-1-(p-Tolyl)ethylamine (R)-1-(p-tolyl)ethan-1-amine (1R)-1-(4-methylphenyl)ethanamine (1R)-(+)-1-(4-Methylphenyl)ethylamine (R)-(+)-α,4-Dimethylbenzylamine (R)-(+)-(4-Methylphenyl)ehtylamine 4187-38-6 Amines Organic Building Blocks Optical Resolution Chiral Building Blocks for Resolution of Acids Amines (Chiral) Asymmetric Synthesis Amines Chiral Building Blocks Organic Building Blocks chiral API intermediates Amines (Chiral) Asymmetric Synthesis Chiral Building Blocks for Resolution of Acids Optical Resolution Synthetic Organic Chemistry