 
        | Pyridoxal 5'-phosphate monohydrate Basic information | 
| Product Name: | Pyridoxal 5'-phosphate monohydrate | 
| Synonyms: | 3-hydroxy-2-methyl-5-((phosphonooxy)methyl)-4-pyridinecarboxaldehydemonohydr;3-hydroxy-2-methyl-5-((phosphonooxy)methyl)-4-pyridinecarboxaldehydmonoh;3-hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde5-phosphatemonohydrat;phosphopyridoxalmonohydrate;pyridoxal,5-(dihydrogenphosphate),monohydrate;5-Phosphate Monohydrate;PYRIDOXAL-5-PHOSPHATEextrapure;Codecarboxylase, PLP, Pyridoxal 5-phosphate, 3-Hydroxy-2-methyl-5-([phosphonooxy]methyl)-4-pyridinecarboxaldehyde | 
| CAS: | 41468-25-1 | 
| MF: | C8H12NO7P | 
| MW: | 265.16 | 
| EINECS: | 609-929-1 | 
| Product Categories: | Aldehydes;Analytical Reagents;Analytical/Chromatography;Building Blocks;C8;Carbonyl Compounds;Chemical Synthesis;Derivatization Reagents;Derivatization Reagents HPLC;Fluorescence;Nutrition Research;Organic Building Blocks;Vitamin B;Vitamin B6;Biochemistry;Vitamin Derivatives;Vitamins | 
| Mol File: | 41468-25-1.mol | 
|  | |
| Pyridoxal 5'-phosphate monohydrate Chemical Properties | 
| Melting point | 140-143 °C(lit.) | 
| storage temp. | 2-8°C | 
| form | Crystalline Powder | 
| color | Pale yellow | 
| Water Solubility | 5 g/L (20 ºC) | 
| Sensitive | Light Sensitive | 
| Merck | 14,7979 | 
| BRN | 234749 | 
| InChIKey | CEEQUQSGVRRXQI-UHFFFAOYSA-N | 
| CAS DataBase Reference | 41468-25-1(CAS DataBase Reference) | 
| Safety Information | 
| Hazard Codes | Xi | 
| Risk Statements | 36/37/38 | 
| Safety Statements | 24/25-36-26 | 
| WGK Germany | 2 | 
| RTECS | UV1208000 | 
| F | 8-10-23 | 
| TSCA | Yes | 
| HS Code | 29333990 | 
| MSDS Information | 
| Provider | Language | 
|---|---|
| 3-Hydroxy-2-methyl-5-([phosphonooxy]methyl)-4-pyridinecarboxaldehyde | English | 
| ACROS | English | 
| SigmaAldrich | English | 
| ALFA | English | 
| Pyridoxal 5'-phosphate monohydrate Usage And Synthesis | 
| Chemical Properties | Pale yellowish white crystalline powder | 
| Uses | 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. |