H-Tyr-ObzlTos

Modify Date: 2025-08-23 19:35:40

H-Tyr-ObzlTos Structure
H-Tyr-ObzlTos structure
 Common Name H-Tyr-ObzlTos
CAS Number 53587-11-4 Molecular Weight 443.513
Density N/A Boiling Point 438.7ºC at 760 mmHg
Molecular Formula C23H25NO6S Melting Point 177 °C
MSDS USA Flash Point 359.8ºC

 Use of H-Tyr-ObzlTos


H-Tyr-OBzl.TosOH is a tyrosine derivative[1].

 Names

Name L-Tyrosine benzyl ester p-toluenesulfonate
Synonym More Synonyms

 H-Tyr-ObzlTos Biological Activity

Description H-Tyr-OBzl.TosOH 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

Boiling Point 438.7ºC at 760 mmHg
Melting Point 177 °C
Molecular Formula C23H25NO6S
Molecular Weight 443.513
Flash Point 359.8ºC
Exact Mass 443.140259
PSA 135.30000
LogP 5.02820
Index of Refraction -13 ° (C=3, MeOH)
Storage condition −20°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn
RIDADR NONH for all modes of transport
WGK Germany 3

 Articles3

More Articles
Effect of protease inhibitors and substrates on 3,5,3'-triiodothyronine binding to rat liver nuclear receptors.

Endocr. Regul. 26 , 127-131, (1992)

The effect of protease inhibitors N-tosyl-L-phenylalanine chloromethyl ketone (TPCK) and N-carbobenzoxy-L-phenylalanine chloromethyl ketone (ZPCK) at concentrations ranging from 1.5 x 10(-6) mol/l to ...

Endosperm-specific expression of tyramine N-hydroxycinnamoyltransferase and tyrosine decarboxylase from a single self-processing polypeptide produces high levels of tyramine derivatives in rice seeds.

Biotechnol. Lett. 31 , 911-915, (2009)

The plant-specific tyramine derivatives, feruloyltyramine (FT) and 4-coumaroyltyramine (CT), represent bioactive compounds found at low levels in many plant species. We generated transgenic rice seeds...

Purification, characterization and partial amino acid sequencing of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase from tobacco cell-suspension cultures.

Eur. J. Biochem. 247 , 1127-1135, (1997)

We report the purification of hydroxycinnamoyl-CoA:tyramine N-(hydroxycinnamoyl)transferase (THT) to apparent homogeneity in 12% yield from tobacco (Nicotiana tabacum L. cv. Xanthi) cell-suspension cu...

 Synonyms

H-Tyr-OBzl.TosOH
H-Tyr-OBzl·Tos-OH
MFCD00038959
EINECS 258-650-8
Benzyl tyrosinate 4-methylbenzenesulfonate (1:1)
L-Tyrosine Benzyl Ester p-Toluenesulfonate
Tyr-OBzl TosOH
L-Tyrosine, O-(phenylmethyl)-, 4-methylbenzenesulfonate (1:1)
O-Benzyl-L-tyrosine 4-methylbenzenesulfonate (1:1)
benzyl (2S)-2-amino-3-(4-hydroxyphenyl)propanoate,4-methylbenzenesulfonic acid
Tyrosine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1)
(S)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoate 4-methylbenzenesulfonate
H-TYR-OBZL·TOS
H-Tyr-ObzlTos
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