H-Pro-NH2.HCl

Names

[ Name ]:
H-Pro-NH2.HCl

[Synonym ]:
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

Biological Activity

[Description]:

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

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[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 â„ƒ

[ 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

Precursor & DownStream

Precursor

DownStream

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%

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...