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N-Methyl-L-leucine hydrochloride (1:1)

Names

[ CAS No. ]:
66866-69-1

[ Name ]:
N-Methyl-L-leucine hydrochloride (1:1)

[Synonym ]:
D-LEUCINE METHYL ESTER HYDROCHLORIDE SALT
N-METHYL-D-LEUCINE HCL
L-Leucine, N-methyl-, hydrochloride (1:1)
D-LEUCINE-OME HCL
N-methyl-L-leucine,hydrochloride
N-Methyl-L-Leucine HCl
(S)-4-methyl-2-(methylamino)pentanoic acid hydrochloride salt
N-Methyl-L-leucin,Hydrochlorid
METHYL D-LEUCINATE HYDROCHLORIDE
N-Methyl-L-leucine hydrochloride (1:1)
H-D-Leu-OBzl.HCl

Biological Activity

[Description]:

(S)-4-Methyl-2-(methylamino)pentanoic acid hydrochloride is a leucine derivative[1].

[Related Catalog]:

Research Areas >> Others
Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

[ Melting Point ]:
159-165 °C

[ Molecular Formula ]:
C7H16ClNO2

[ Molecular Weight ]:
181.660

[ Exact Mass ]:
181.086960

[ PSA ]:
49.33000

[ LogP ]:
1.89800

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
36/37

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2922499990

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2922499990

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%


Related Compounds