L-Prolinamide

Modify Date: 2024-01-02 12:19:18

L-Prolinamide Structure
L-Prolinamide structure
Common Name L-Prolinamide
CAS Number 7531-52-4 Molecular Weight 114.146
Density 1.1±0.1 g/cm3 Boiling Point 303.6±31.0 °C at 760 mmHg
Molecular Formula C5H10N2O Melting Point 95-97 °C(lit.)
MSDS Chinese USA Flash Point 137.4±24.8 °C

 Use of L-Prolinamide


L-Prolinamide is a proline derivative[1].

 Names

Name L-prolinamide
Synonym More Synonyms

 L-Prolinamide Biological Activity

Description L-Prolinamide 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

Density 1.1±0.1 g/cm3
Boiling Point 303.6±31.0 °C at 760 mmHg
Melting Point 95-97 °C(lit.)
Molecular Formula C5H10N2O
Molecular Weight 114.146
Flash Point 137.4±24.8 °C
Exact Mass 114.079315
PSA 55.12000
LogP -1.51
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.491

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xn: Harmful;
Risk Phrases R22
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2933990090

 Synthetic Route

 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%

 Articles27

More Articles
Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Nat. Chem. Biol. 5 , 45-52, (2009)

Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting tr...

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...

d-Glucosamine in a chimeric prolinamide organocatalyst for direct asymmetric aldol addition

Carbohydr. Res. 356 , 273-7, (2012)

O-TBDPS D-glucosamine coupled with l-proline is reported to act as an efficient organocatalyst in the accomplishment of direct aldol reactions. Excellent results, in terms of chemical yields, as well ...

 Synonyms

(S)-Prolinamide
2-Pyrrolidinecarboxamide, (S)-
(2S)-2-Pyrrolidinecarboxamide
h-pro-nh2
2-Pyrrolidinecarboximidic acid, (2S)-
(S)-Pyrrolidine-2-carboxylic acid amide
MFCD00005253
(2S)-2-Pyrrolidinecarboximidic acid
EINECS 231-397-0
2-Pyrrolidinecarboxamide, (2S)-
(S)-pyrrolidine-2-carboxamide
L-Prolinamide
(2S)-pyrrolidine-2-carboxamide
Prolinamide
L-proline amide
L-Prolineamide
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