Top Quality Natural...

Top Quality Natural Pyridoxal 5'-phosphate monohydrate
Top Quality Natural Pyridoxal 5'-phosphate monohydrate
Top Quality Natural Pyridoxal 5'-phosphate monohydrate
Top Quality Natural Pyridoxal 5'-phosphate monohydrate

Top Quality Natural Pyridoxal 5'-phosphate monohydrate

Min.Order / FOB Price:Get Latest Price

1 Kilogram

FOB Price:USD 5.0000 -7.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : T/T,Other

Keywords

Pyridoxal 5'-phosphate monohydrate 41468-25-1 P5P

Quick Details

  • Appearance:white powder
  • Application:Pharmaceutical;Food Preservative;Cosmetics;Food
  • PackAge:1kg/bag,5kg/bag,25kg/drum
  • ProductionCapacity:5000|Kilogram|Month
  • Storage:in a cool&dry place
  • Transportation:By air,By Sea

Superiority:

41468-25-1 - Physico-chemical Properties

Molecular Formula C8H12NO7P
Molar Mass 265.16
Melting Point 140-143°C(lit.)
Boling Point 565.7°C at 760 mmHg
Flash Point 296°C
Water Solubility 5 g/L (20 ºC)
Solubility alkaline solutions; sparingly soluble in water
Vapor Presure 1.23E-13mmHg at 25°C
Appearance Powder
Color Pale yellow
Merck 14,7979
BRN 234749
Storage Condition 2-8°C
Stability Air Sensitive, Moisture Sensitive
Sensitive Light Sensitive
MDL MFCD00149414
Use Enzyme cofactor. Coenzyme form of vitamin B6.

 

introduction pyridoxal phosphate (PLP, the main metabolically active form of vitamin B6) is a multifunctional coenzyme involved in the metabolism of amino compounds. enzymes with it as coenzyme factors are called PLP-dependent enzymes (PLP-dependent enzymes, PLP-DEs), which play an important role in the metabolism of sugars, lipids and amino acids. It is mainly the biosynthesis of amino acids and biomolecules, such as neurotransmitters serotonin, dopamine, epinephrine, norepinephrine, gamma-aminobutyric acid (GABA) and histamine.
Function PLP is very important. It participates in the activities of more than 140 PLP-dependent enzymes, accounting for about 4% of all classification activities. The versatility of PLP comes from its electrophilicity: PLP covalently binds to the substrate by forming an external aldimine at the beginning of the reaction, and then different types of carbanion reaction intermediates can be stabilized by PLP through resonance effect. This function of PLP is also called "electron trap". In addition to the electron absorption effect, since almost all PLP-dependent reactions generate cationic and anionic intermediates, acidic and basic groups that assist in proton transfer are equally important.
application pyridoxal 5-phosphate is an organic synthesis intermediate and a pharmaceutical intermediate, which can be used as a biochemical reagent in the laboratory organic synthesis process and chemical medicine research and development process.
synthesis method a synthesis method of pyridoxal phosphate, at least comprising the following steps: step 1, using active manganese dioxide as a catalyst, pyridoxine hydrochloride is oxidized to pyridoxal hydrochloride; step 2, the pyridoxal hydrochloride and N,N-dimethylethylenediamine are condensed to obtain pyridoxal condensate; step 3, the pyridoxal condensate and polyphosphoric acid phosphorylation reaction to prepare pyridoxal phosphate crude.
biological activity Pyridoxal 5-phosphate monohydrate is an active vitamin B6 metabolite and a cofactor in many amino acid metabolic reactions.
use enzyme cofactor; Vitamin normal coenzyme form of B6

 

 

 

Details:

Pyridoxal 5'-phosphate monohydrate

Mol Download Chemical properties

CAS:

41468-25-1

MF:

C8H12NO7P

MW:

265.16

EINECS:

609-929-1

MDL No.:

MFCD00149414

Properties

Melting point:

140-143 °C(lit.)

storage temp. 

2-8°C

solubility 

Acetonitrile (Slightly), DMSO (Slightly)

form 

Crystalline Powder

color 

Pale yellow

Water Solubility 

5 g/L (20 ºC)

Sensitive 

Light Sensitive

Merck 

14,7979

BRN 

234749

Stability:

Air Sensitive, Moisture Sensitive

InChI

InChI=1S/C8H10NO6P.H2O/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14;/h2-3,11H,4H2,1H3,(H2,12,13,14);1H2

InChIKey

CEEQUQSGVRRXQI-UHFFFAOYSA-N

SMILES

C1(COP(=O)(O)O)=CN=C(C)C(O)=C1C=O.O

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