H-Leu-Oet.HCl

Modify Date: 2024-01-02 10:06:31

H-Leu-Oet.HCl Structure
H-Leu-Oet.HCl structure
Common Name H-Leu-Oet.HCl
CAS Number 2743-40-0 Molecular Weight 195.687
Density 0.944g/cm3 Boiling Point 191.4ºC at 760 mmHg
Molecular Formula C8H18ClNO2 Melting Point 134-136 °C
MSDS USA Flash Point 62.9ºC

 Use of H-Leu-Oet.HCl


H-Leu-OEt.HCl is a leucine derivative[1].

 Names

Name ethyl (2S)-2-amino-4-methylpentanoate,hydrochloride
Synonym More Synonyms

 H-Leu-Oet.HCl Biological Activity

Description H-Leu-OEt.HCl is a leucine derivative[1].
Related Catalog
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

Density 0.944g/cm3
Boiling Point 191.4ºC at 760 mmHg
Melting Point 134-136 °C
Molecular Formula C8H18ClNO2
Molecular Weight 195.687
Flash Point 62.9ºC
Exact Mass 195.102600
PSA 52.32000
LogP 2.42520
Vapour Pressure 0.515mmHg at 25°C
Index of Refraction 19 ° (C=5, EtOH)
Storage condition 2-8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922499990

 Synthetic Route

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H-Leu-Oet.HCl Structure

H-Leu-Oet.HCl

CAS#:2743-40-0

Literature: Sun, Chuanwen; Zhu, Jun; Wang, Haifeng; Jin, Jia; Xing, Jiahua; Yang, Dingrong European Journal of Medicinal Chemistry, 2011 , vol. 46, # 1 p. 11 - 20

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H-Leu-Oet.HCl Structure

H-Leu-Oet.HCl

CAS#:2743-40-0

Literature: E. R. Squibb and Sons, Inc. Patent: US4885292 A1, 1989 ;

~%

H-Leu-Oet.HCl Structure

H-Leu-Oet.HCl

CAS#:2743-40-0

Literature: Meppen, Malte; Pacini, Barbara; Bazzo, Renzo; Koch, Uwe; Leone, Joseph F.; Koeplinger, Kenneth A.; Rowley, Michael; Altamura, Sergio; Di Marco, Annalise; Fiore, Fabrizio; Giuliano, Claudio; Gonzalez-Paz, Odalys; Laufer, Ralph; Pucci, Vincenzo; Narjes, Frank; Gardelli, Cristina European Journal of Medicinal Chemistry, 2009 , vol. 44, # 9 p. 3765 - 3770

 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%

 Articles2

More Articles
Glutamate formation via the leucine-to-glutamate pathway of rat pancreas.

Am. J. Physiol. Gastrointest. Liver Physiol. 306(11) , G938-46, (2014)

The leucine-to-glutamate (Leu→Glu) pathway, which metabolizes the carbon atoms of l-leucine to form l-glutamate, was studied by incubation of rat tissue segments with l-[U-(14)C]leucine and estimation...

Synthesis of homopolypeptides by aminolysis mediated by proteases encapsulated in silica nanospheres.

Macromol. Biosci. 14(11) , 1619-26, (2014)

We report the encapsulation of three different proteases in bioinspired silica. Silica particles were formed under mild reaction conditions using cationic amine-rich ethyleneamines as initiators, whic...

 Synonyms

dl-leucine ethyl ester hydrochloride
EINECS 220-375-6
(S)-Ethyl 2-amino-4-methylpentanoate hydrochloride
H-Leu-Oet.HCl
Ethyl L-isoleucinate hydrochloride (1:1)
EthylL-leucinatehydrochloride
H-Leu-OEt·HCl
L-Leucine Ethyl Ester Hydrochloride
L-Isoleucine, ethyl ester, hydrochloride (1:1)
MFCD00034879
leu-OEt HCl
L-LEUCINE ETHYL ESTER HCl
Ethyl 2-Amino-4-Methylpentanoate
ethyl 2-amino-4-methylpentanoate hydrochloride
L-leucine-OEt HCl
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