L-Prolinamide hydrochloride structure, CAS 42429-27-6

L-Prolinamide hydrochloride

CAS Number42429-27-6

SynonymsEINECS 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

Molecular FormulaC5H11ClN2O

Molecular Weight186.59

Purity97%

Density

Boiling Point

Melting Point178-182 ℃

Flash Point

Appearancesolid

EINECS

MSDSChineseEnglish

Symbol

Signal Word

Cat. No.: 2A-9042969 Purity: 97%
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Quality Control of [ 42429-27-6 ] Purity: 97% SDS Specification MoL

Chemical & Physical Properties
CAS Number42429-27-6
Catalog No.2A-9042969
Chinese NameL-脯氨酰胺盐酸盐
SynonymsEINECS 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
Molecular FormulaC5H11ClN2O
Molecular Weight186.59
Purity97
Melting Point178-182 ℃
Appearancesolid
Storage Condition-15°C
Application(S)-pyrrolidine-2-carboxamide hydrochloride is a proline derivative [1].
HTC2933990090
PubChem ID329763452
MDL NumberMFCD06797014
SMILESCl.NC(=O)[C@@H]1CC(F)(F)CN1
InChI1S/C5H8F2N2O.ClH/c6-5(7)1-3(4(8)10)9-2-5;/h3,9H,1-2H2,(H2,8,10);1H/t3-;/m0./s1
InChI KeyRRQDQYAEZGKHOB-DFWYDOINSA-N
NACRES CodeNA.22
UNSPSC12352005
MSDSmsds/42969_1_42429_27_6.pdf
Use of(S)-Pyrrolidine-2-carboxamide hydrochloride is a proline derivative[1]. Properties 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 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 Exact Mass 150.055984 PSA 55.12000 LogP 1.05480 InChIKey CSKSDAVTCKIENY-WCCKRBBISA-N Safety Information Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter RIDADR NONH for all modes of transport WGK Germany 3 HS Code 2933990090 Precursor & DownStream Precursor 4 CAS#:35150-07-3 Boc-Pro-NH2 CAS#:3392-10-7 N-T-BOC-L-PROLI... CAS#:2133-40-6 H-Pro-OMe.HCl CAS#:76409-77-3 Ac-Aib-L-Pro-NH2 DownStream 3 CAS#:50654-97-2 tert-butyl 5-[(... CAS#:29133-55-9 TERT-BUTYL ((S)... CAS#:147-85-3
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: 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%
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