H-Pro-NH2.HCl

Modify Date: 2024-01-04 06:36:41

H-Pro-NH2.HCl Structure
H-Pro-NH2.HCl structure
Common Name H-Pro-NH2.HCl
CAS Number 42429-27-6 Molecular Weight 150.607
Density N/A Boiling Point N/A
Molecular Formula C5H11ClN2O Melting Point 178-182 ℃
MSDS USA Flash Point N/A

 Use of H-Pro-NH2.HCl


(S)-Pyrrolidine-2-carboxamide hydrochloride is a proline derivative[1].

 Names

Name (2S)-pyrrolidine-2-carboxamide,hydrochloride
Synonym More Synonyms

 H-Pro-NH2.HCl Biological Activity

Description (S)-Pyrrolidine-2-carboxamide hydrochloride is a proline 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

Melting Point 178-182 ℃
Molecular Formula C5H11ClN2O
Molecular Weight 150.607
Exact Mass 150.055984
PSA 55.12000
LogP 1.05480
Storage condition -15°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Safety Phrases 22-24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles4

More Articles
Enantioseparation of amino acids and alpha-hydroxy acids on ligand-exchange continuous beds by capillary electrochromatography.

Electrophoresis 31 , 1517-1520, (2010)

A new chiral stationary phase based on continuous bed (CB) technology using L-prolinamide as a chiral selector was prepared. Its ability for enantioseparation of amino acids and alpha-hydroxy acids by...

Enantioseparation by chromatographic and electromigration techniques using ligand-exchange as chiral separation principle.

Anal. Bioanal. Chem 400 , 2305-2316, (2011)

This article gives a short overview of the application of the principle of chiral ligand-exchange in HPLC, CE, and CEC. Since its introduction by Davankov, more than thousand articles have appeared in...

Chiral separation of NBD-amino acids by ligand-exchange micro-channel electrophoresis.

Anal. Sci. 21 , 67-71, (2005)

The chiral separation of amino acid derivatives by ligand-exchange electrophoresis in a microchannel chip was performed for the first time. A Cu(II) complex with L-prolinamide was used as a chiral sel...

 Synonyms

EINECS 255-818-2
L-Proline amide hydrochloride
HCl*H-L-Pro-NH2
L-Prolinamidehydrochloride
Prolinamide hydrochloride (1:1)
2-Pyrrolidinecarboxamide, (2S)-, hydrochloride (1:1)
dl-prolinamide hydrochloride
MFCD00058156
Pro-NH2*HCl
2-Pyrrolidinecarboxamide, hydrochloride (1:1)
L-Prolinamide hydrochloride (1:1)
L-Prolinamide HCl
H-Pro-NH2.HCl
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