Nipecotic acid

• Catalog No.: 211672
• CAS Number: 498-95-3
• M. F.: C6H11NO2
• M. W.: 129.15704
• Purity: 98%

SYNONYMS

• Title: 3-哌啶甲酸
• IUPAC name: piperidine-3-carboxylic acid
• IUPAC Traditional name: nipecotic acid
• Synonyms: (±)-β-Homoproline; Hexahydronicotinic acid; 3-Piperidinecarboxylic acid; 3-Carboxypiperidine; 3-甲酸哌啶

DATABASE IDS

• EC Number: 207-873-9
• PubChem SID: 24278161
• MDL Number: MFCD00005992
• CAS Number: 498-95-3

PROPERTIES

• Empirical Formula (Hill Notation): C6H11NO2
• Purity: 98%
• Gene Information: human ... SLC23A2(9962)
• Melting Point: 261 °C (dec.)(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
25 g in poly bottle
Application
Reactant for concurrent esterification and N-acteylation of amino acids with orthoesters1Reactant for synthesis of: Anticonvulsants2 HCV NS5B polymerase inhibitors3 Cathepsin S inhibitors4 Orally bioavailable P2Y12 antagonists for inhibition of platelet aggregation5 Positive allosteric modulator of metabotropic glutamate receptor 46
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 211672.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

Description (简体中文)

包装
1, 5 g in glass bottle
25 g in poly bottle
Application
Reactant for concurrent esterification and N-acteylation of amino acids with orthoesters1Reactant for synthesis of: Anticonvulsants2 HCV NS5B polymerase inhibitors3 Cathepsin S inhibitors4 Orally bioavailable P2Y12 antagonists for inhibition of platelet aggregation5 Positive allosteric modulator of metabotropic glutamate receptor 46
Other Notes
Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 211672.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.