H-Leu-Oet.HCl structure
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Common Name | H-Leu-Oet.HCl | ||
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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.HClH-Leu-OEt.HCl is a leucine derivative[1]. |
Name | ethyl (2S)-2-amino-4-methylpentanoate,hydrochloride |
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Synonym | More Synonyms |
Description | H-Leu-OEt.HCl is a leucine derivative[1]. |
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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 |
Density | 0.944g/cm3 |
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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 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
HS Code | 2922499990 |
~% 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 |
~% H-Leu-Oet.HCl CAS#:2743-40-0 |
Literature: E. R. Squibb and Sons, Inc. Patent: US4885292 A1, 1989 ; |
~% 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 |
Precursor 3 | |
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DownStream 7 | |
HS Code | 2922499990 |
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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% |
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... |
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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... |
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 |