CAS 721-90-4|H-Phe-Gly-OH

Introduction:Basic information about CAS 721-90-4|H-Phe-Gly-OH, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameH-Phe-Gly-OH
CAS Number721-90-4Molecular Weight222.24000
Density1.259g/cm3Boiling Point512.5ºC at 760 mmHg
Molecular FormulaC11H14N2O3Melting Point-260ºC (dec.)
MSDSChineseUSAFlash Point263.7ºC

Names

Nameh-phe-gly-oh
SynonymMore Synonyms

H-Phe-Gly-OH BiologicalActivity

DescriptionPhe-Gly hydrate is a Glycine (HY-Y0966) derivative[1].
Related CatalogResearch Areas >>OthersSignaling Pathways >>Others >>Others
In VitroAmino 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

Density1.259g/cm3
Boiling Point512.5ºC at 760 mmHg
Melting Point-260ºC (dec.)
Molecular FormulaC11H14N2O3
Molecular Weight222.24000
Flash Point263.7ºC
Exact Mass222.10000
PSA92.42000
LogP0.84840
Index of Refraction1.576
InChIKeyGLUBLISJVJFHQS-UHFFFAOYSA-N
SMILESNC(Cc1ccccc1)C(=O)NCC(=O)O
Storage condition-20C

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADRNONH for all modes of transport
HS Code2924299090

Customs

HS Code2924299090
Summary2924299090. 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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