Pyridoxal 5′-phosphate monohydrate

• Catalog No.: 82870
• CAS Number: 41468-25-1
• M. F.: C8H12NO7P
• M. W.: 265.157141
• Purity: ≥97.0% (NT)

SYNONYMS

• IUPAC name: [(4-formyl-5-hydroxy-6-methylpyridin-3-yl)methoxy]phosphonic acid hydrate
• IUPAC Traditional name: hydrate pyridoxal phosphate
• Synonyms: Codecarboxylase; Pyridoxal 5-phosphate; PLP; P5P; 3-Hydroxy-2-methyl-5-([phosphonooxy]methyl)-4-pyridinecarboxaldehyde

DATABASE IDS

• PubChem SID: 24888057
• Beilstein Number: 234749
• CAS Number: 41468-25-1
• MDL Number: MFCD00149414

PROPERTIES

• Antion Traces: chloride (Cl-): ≤500 mg/kg
• Antion Traces: sulfate (SO42-): ≤50 mg/kg
• Cation Traces: Ca: ≤20 mg/kg
• Cation Traces: Cd: ≤5 mg/kg
• Cation Traces: Co: ≤5 mg/kg
• Cation Traces: Cr: ≤5 mg/kg
• Cation Traces: Cu: ≤5 mg/kg
• Cation Traces: Fe: ≤50 mg/kg
• Cation Traces: K: ≤50 mg/kg
• Cation Traces: Mg: ≤5 mg/kg
• Cation Traces: Mn: ≤5 mg/kg
• Cation Traces: Na: ≤2000 mg/kg
• Cation Traces: Ni: ≤5 mg/kg
• Cation Traces: Pb: ≤5 mg/kg
• Cation Traces: Zn: ≤5 mg/kg
• Empirical Formula (Hill Notation): C8H10NO6P · H2O
• Purity: ≥97.0% (NT)
• Melting Point: 140-143 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• RTECS: UV1208000
• Storage Temperature: 2-8°C
• German water hazard class: 2

DETAILS

Description (English)

Other Notes
Coenzymes and Cofactors, vol. 1: Vitamin B6, Pyridoxal Phosphate1,2
Application
Pyridoxal 5-phosphate (PLP) (active form of Vitamin B6) is an enzyme prosthetic group that acts as a coenzyme in transamination, decarboxylation and deamination reactions such as the conversion of dopa into dopamine; of glutamate into GABA; of histidine to histamine. PLP works mechanistically through formation of a Schiff-base.

Description (简体中文)

Other Notes
Coenzymes and Cofactors, vol. 1: Vitamin B6, Pyridoxal Phosphate1,2
Application
Pyridoxal 5-phosphate (PLP) (active form of Vitamin B6) is an enzyme prosthetic group that acts as a coenzyme in transamination, decarboxylation and deamination reactions such as the conversion of dopa into dopamine; of glutamate into GABA; of histidine to histamine. PLP works mechanistically through formation of a Schiff-base.