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. |