H-Leu-Oet.HCl

Suppliers

Names

[ Name ]:
H-Leu-Oet.HCl

[Synonym ]:
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

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

MSDS

Click to get detail MSDS

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

Click to get detail synthetic route

Precursor & DownStream

Precursor

Ethanol
L-leucine
(L)-N-Boc leucine ethyl ester

DownStream

L-(+)-Leucinol
Leucine,N-[N-(benzylsulfonyl)-L-leucyl]-, ethyl ester, L- (8CI)
Z-Gly-Leu-OH
Boc-Leu-Leu-OH
(S)-(-)-2-ACETOXYPROPIONYLCHLORIDE
ethyl 2-isothiocyanato-4-methylpentanoate
ethyl 2-isocyanato-4-methylvalerate

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%

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...

H-Leu-OEt.HCl
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H-D-Leu-Oet.HCl
H-Leu-Oall.TosOH
H-Leu-Ser-Lys-Leu-NH2 trifluoroacetate salt
H-Leu-Ser-p-nitro-Phe-Nle-Ala-Leu-OMe trifluoroacetate salt
2-(3,4-difluorobenzyl)-4-(5-ethyl-1,2,4-oxadiazol-3-yl)-5,6,7,8-tetrahydro-1H-pyrido[1,2-c]pyrimidine-1,3(2H)-dione
4-Chloro-6-ethyl-2-(2-fluorophenyl)pyrimidine
2-benzyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)-6,7,8,9-tetrahydropyrimido[1,6-a]azepine-1,3(2H,5H)-dione
4-(5-methyl-1,2,4-oxadiazol-3-yl)-2-[4-(trifluoromethoxy)benzyl]-6,7,8,9-tetrahydropyrimido[1,6-a]azepine-1,3(2H,5H)-dione
2-(2-methylbenzyl)-4-(5-methyl-1,2,4-oxadiazol-3-yl)-6,7,8,9-tetrahydropyrimido[1,6-a]azepine-1,3(2H,5H)-dione
N-(3-methoxyphenyl)-2-[4-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-dioxo-3,5,6,7,8,9-hexahydropyrimido[1,6-a]azepin-2(1H)-yl]acetamide
N-(2-ethylphenyl)-2-[4-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-dioxo-3,5,6,7,8,9-hexahydropyrimido[1,6-a]azepin-2(1H)-yl]acetamide
2-[4-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-dioxo-3,5,6,7,8,9-hexahydropyrimido[1,6-a]azepin-2(1H)-yl]-N-(2-methylphenyl)acetamide
4-Chloro-2-(2-fluorophenyl)-6-isopropylpyrimidine
N-(2,4-dimethylphenyl)-2-[4-(5-methyl-1,2,4-oxadiazol-3-yl)-1,3-dioxo-3,5,6,7,8,9-hexahydropyrimido[1,6-a]azepin-2(1H)-yl]acetamide

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