H-Tyr-OMe.HCl

Modify Date: 2024-01-02 10:33:57

H-Tyr-OMe.HCl Structure
H-Tyr-OMe.HCl structure
 Common Name H-Tyr-OMe.HCl
CAS Number 3417-91-2 Molecular Weight 231.676
Density 1.21g/cm3 Boiling Point 330ºC at 760 mmHg
Molecular Formula C10H14ClNO3 Melting Point 192 °C (dec.)(lit.)
MSDS USA Flash Point 153.4ºC

 Use of H-Tyr-OMe.HCl


H-Tyr-OMe.HCl is a tyrosine derivative[1].

 Names

Name Methyl L-tyrosinate hydrochloride
Synonym More Synonyms

 H-Tyr-OMe.HCl Biological Activity

Description H-Tyr-OMe.HCl is a tyrosine 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 1.21g/cm3
Boiling Point 330ºC at 760 mmHg
Melting Point 192 °C (dec.)(lit.)
Molecular Formula C10H14ClNO3
Molecular Weight 231.676
Flash Point 153.4ºC
Exact Mass 231.066223
PSA 72.55000
LogP 1.93730
Index of Refraction 13 ° (C=2, MeOH)
Storage condition 2~8°C

 Safety Information

Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 29225000

 Synthetic Route

 Customs

HS Code 2922509090
Summary 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles17

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...
Novel molecular combination deriving from natural aminoacids and polyphenols: Design, synthesis and free-radical scavenging activities.

Eur. J. Med. Chem. 50 , 383-92, (2012)

Following the recent output of scientific publications in the matter of synergic activity between different antioxidants, we have undertaken the present study with the aim to synthesize new molecules ...
Aromatic amino acid methyl ester analogs form quinonoidal species with Dopa decarboxylase.

FEBS Lett. 412(1) , 245-8, (1997)

This study reports for the first time that binding of aromatic methyl ester analogs to Dopa decarboxylase in the native and inactive nicked forms causes the appearance of a dead-end quinonoidal specie...

 Synonyms

Methyl L-tyrosinate hydrochloride
L-Tyrosine Methylester HLC
L-TyrOCH3 hydrochloride
Tyr-OmeHCl
(S)-2-Amino-3-(4-hydroxyphenyl)propionic acid methyl ester hydrochloride
methyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate hydrochloride
METHYL TYROSINATE HCL
EINECS 222-313-3
Tyrosine methyl ester hydrochloride, L-
L-Tyrosine Methyl Ester Hydrochloride
TYROSINE-OME HCL
L-TYROSINE METHYL ESTER HCL
L-Tyrosine, methyl ester, hydrochloride (1:1)
H-L-TYR-OME HCL
H-Tyr-OMe·HCl
(S)-Methyl 2-amino-3-(4-hydroxyphenyl)propanoate hydrochloride
L-Tyrosine, methyl ester, hydrochloride
L-Tyr-OMe.HCL
MethylL-tyrosinatehydrochloride
L-Tyr-OMe hydrochloride
MFCD00012607
L-Tyr methyl ester hydrochloride
QR D1YZVO1 &&L Form HCl
L-Tyrosinemethylesterhydrochloride
Methyl L-tyrosinate hydrochloride (1:1)
H-Tyr-Ome HCl
H-Tyr-OMe.HCl
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