H-Phe-Gly-OH

Modify Date: 2025-08-25 18:26:14

H-Phe-Gly-OH Structure
H-Phe-Gly-OH structure
Common Name H-Phe-Gly-OH
CAS Number 721-90-4 Molecular Weight 222.24000
Density 1.259g/cm3 Boiling Point 512.5ºC at 760 mmHg
Molecular Formula C11H14N2O3 Melting Point -260ºC (dec.)
MSDS Chinese USA Flash Point 263.7ºC

 Use of H-Phe-Gly-OH


Phe-Gly hydrate is a Glycine (HY-Y0966) derivative[1].

 Names

Name h-phe-gly-oh
Synonym More Synonyms

 H-Phe-Gly-OH Biological Activity

Description Phe-Gly hydrate is a Glycine (HY-Y0966) 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 1.259g/cm3
Boiling Point 512.5ºC at 760 mmHg
Melting Point -260ºC (dec.)
Molecular Formula C11H14N2O3
Molecular Weight 222.24000
Flash Point 263.7ºC
Exact Mass 222.10000
PSA 92.42000
LogP 0.84840
Index of Refraction 1.576
Storage condition -20C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
HS Code 2924299090

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles19

More Articles
Hydrogen exchange equilibria in thiols.

Chem. Res. Toxicol. 25(9) , 1862-7, (2012)

Cysteine, cysteinyl-glycine, glutathione, phenylalanyl-cysteinyl-glycine, and histidyl-cysteinyl-glycine were dissolved in acidic and neutral D(2)O in the presence of the radical generator 2,2'-azobis...

Enhanced transdermal delivery of phenylalanyl-glycine by chemical modification with various fatty acids.

Int. J. Pharm. 250(1) , 119-28, (2003)

We synthesized three novel lipophilic derivatives of phenylalanyl-glycine (Phe-Gly), C4-Phe-Gly, C6-Phe-Gly and C8-Phe-Gly by chemical modification with butyric acid (C4), caproic acid (C6) and octano...

Enhancement of the small intestinal uptake of phenylalanylglycine via a H+/oligopeptide transport system by chemical modification with fatty acids.

Life Sci. 61(25) , 2455-65, (1997)

The transport characteristics of chemically modified phenylalanylglycine (Phe-Gly) with butyric acid (C4-Phe-Gly) and caproic acid (C6-Phe-Gly) were examined using rabbit intestinal brush-border membr...

 Synonyms

Phe-Gly-OH
Phe-glycrystalline
L-Phenylalanyl-glycin
phenylalanylglycine
Phe-Gly hydrate
L-Phe-Gly-OH
L-PHENYLALANYLGLYCINE
phenylalanyl-glycin
phenylalanineglycine
PHE-GLY
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