L-Prolinamide

Modify Date: 2025-08-20 17:44:24

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
InChIKey VLJNHYLEOZPXFW-BYPYZUCNSA-N
SMILES NC(=O)C1CCCN1

 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 ...

 L-ProlinamideBioassay

View more

Name: Phenotypic growth assay for Mycobacterium tuberculosis grown for 4 days on DPPC, chol...
Source: ChEMBL
Target: N/A
External Id: CHEMBL4649948
Name: Phenotypic growth assay for Mycobacterium tuberculosis grown for 3 days on 7H9, gluco...
Source: ChEMBL
Target: N/A
External Id: CHEMBL4649949
Name: Cell survival assay for modulators of telomere damage signalling
Source: 15378
Target: N/A
External Id: TELO_02
Name: Antibacterial activity against Acinetobacter baumannii ATCC 19606 (CO-ADD:GN_034); MI...
Source: ChEMBL
Target: Acinetobacter baumannii
External Id: CHEMBL4296188
Name: Antibacterial activity against Pseudomonas aeruginosa ATCC 27853 (CO-ADD:GN_042); MIC...
Source: ChEMBL
Target: Pseudomonas aeruginosa
External Id: CHEMBL4296187
Name: Inhibition of nitrogen-starved wild type sigma1278b yeast Gap1-mediated amino acid up...
Source: ChEMBL
Target: General amino-acid permease GAP1
External Id: CHEMBL1228071
Name: qHTS for Inhibitors of Polymerase Kappa
Source: NCGC
Target: DNA polymerase kappa [Homo sapiens]
External Id: PolK100
Name: Antibacterial activity against Pseudomonas aeruginosa PAO397 [PAO1 d(mexAB-oprM) d(me...
Source: ChEMBL
Target: Pseudomonas aeruginosa
External Id: CHEMBL4296802
Name: qHTS for Inhibitors of binding or entry into cells for Marburg Virus
Source: NCGC
Target: gene 4 small orf - Marburg virus
External Id: VSVM-OFFLINE
Name: HIV Cellular Data
Source: NIAID
Target: N/A
External Id: HIV Cellular Data
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 Synonyms

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