ChemicalBook > CAS DataBase List > Pyridoxal 5’-Phosphate

Pyridoxal 5’-Phosphate

Product Name
Pyridoxal 5’-Phosphate
CAS No.
853645-22-4
Chemical Name
Pyridoxal 5’-Phosphate
Synonyms
Pyridoxal 5’3-Hydroxy-2-methyl-5;-phosphate (hydrate);PYRIDOXAL-5-PHOSPHATE;pyridoxa 5' phosphate;PYRIDOXAL-5'-PHOSPHATE;Pyridoxaol-5-phosphate;rubber accelerator MBTS;Pyridoxal-[d3] Phosphate;Pyridoxal 5'-phosphate hydrate
CBNumber
CB22131140
Molecular Formula
C8H10NO6P
Formula Weight
247.14
MOL File
853645-22-4.mol
More
Less

Pyridoxal 5’-Phosphate Property

Melting point:
140-143 ºC
storage temp. 
-20°C
solubility 
DMSO (Slightly, Heated), Methanol (Slightly), Water (Slightly)
pka
pKa 8.69(H2O t = 25 I = 0.15)(Approximate)
form 
powder
color 
White to Pale Yellow
Odor
Odorless
BRN 
234749
Stability:
Hygroscopic
More
Less

Safety

WGK Germany 
3
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
P9255
Product name
Pyridoxal 5′-phosphate hydrate
Purity
≥98%
Packaging
1g
Price
$57.4
Updated
2024/03/01
Sigma-Aldrich
Product number
P3657
Product name
Pyridoxal 5′-phosphate hydrate
Purity
powder, BioReagent, suitable for cell culture
Packaging
1g
Price
$78.8
Updated
2024/03/01
Cayman Chemical
Product number
20352
Product name
Pyridoxal 5'-phosphate (hydrate)
Purity
≥95%
Packaging
1g
Price
$44
Updated
2024/03/01
Cayman Chemical
Product number
20352
Product name
Pyridoxal 5'-phosphate (hydrate)
Purity
≥95%
Packaging
5g
Price
$151
Updated
2024/03/01
Sigma-Aldrich
Product number
P9255
Product name
Pyridoxal 5′-phosphate hydrate
Purity
≥98%
Packaging
5g
Price
$207
Updated
2024/03/01
More
Less

Pyridoxal 5’-Phosphate Chemical Properties,Usage,Production

Uses

Enzyme cofactor.Normal coenzyme form of Vitamin B6

Uses

Pyridoxal 5′-phosphate hydrate has also been used:

  • as a reference standard to quantify vitamin B6 in feed and digesta samples using high performance liquid chromatography (HPLC)
  • in D-amino acid transaminase reaction(10)
  • as a cofactor for L-glutamic acid decarboxylase

Definition

ChEBI: Pyridoxal 5'-phosphate is the monophosphate ester obtained by condensation of phosphoric acid with the primary hydroxy group of pyridoxal. It has a role as a coenzyme, a human metabolite, an Escherichia coli metabolite, a Saccharomyces cerevisiae metabolite, a mouse metabolite, an EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor and a cofactor. It is a vitamin B6 phosphate, a member of methylpyridines, a monohydroxypyridine and a pyridinecarbaldehyde. It is functionally related to a pyridoxal. It is a conjugate acid of a pyridoxal 5'-phosphate(2-).

General Description

Pyridoxal 5′-phosphate (PLP) is synthesized in a multiple-step process. The two pathways inlcude pyridoxal phosphate biosynthetic protein (PdxA)- pyridoxine-5′-phosphate synthase (PdxJ) pathway and the pyridoxal 5′-phosphate synthase subunit PDX1/PDX2 pathway. It is the active form of pyridoxine.

Biochem/physiol Actions

Pyridoxal 5′-phosphate (PLP) aids in carbohydrate and fat metabolism by serving as a cofactor. It is majorly responsible for catalyzing the enzymatic reactions involved in sphingolipid synthesis and neurotransmitter (dopamine and serotonin) synthesis. PLP is used in the studies of PLP-dependent enzyme active sites. PLP is also a cofactor for a wide range of enzymes including mitochondrial 5-Aminolevulinic acid synthase (ALAS) cysteine desulfurase, cystathionine γ-synthase (CGS), ornithine 4,5-aminomutase (OAM), and D-serine dehydratase.

Biotechnological Applications

Pyridoxal 5’-Phosphate(PLP) is also often employed as an inhibitor and site-directed, conformationally sensitive reporter group for studying the environment of reactive amino groups within proteins. PLP forms aldimine adducts that can be reduced with nucleophilic reducing reagents such as sodium borohydride or sodium cyanoborohydride. Solid PLP is light-sensitive, and solutions should be prepared fresh. There are four pKa values associated with this coenzyme: a pKa < 2.5 and another at 6.20 for the phosphate group, a pKa of 4.14 for the hydroxyl group, and a pKa of 8.69 for the pyridinium group.

Synthesis

A process for the synthesis ofpyridoxal5' -phosphate, comprising the steps of:
a) adding phenetidine into pyridoxal solution, and reacting to generate pyridoxal Schiff base;
b) adding pyridoxal Schiff base into ionic liquid, and stirring until the pyridoxal Schiff base is fully dissolved to obtain an ion mixed solution; adding pyridoxal Schiff base into ionic liquid, stirring at 35-45 ℃, and cooling the obtained ionic mixed solution to room temperature after the pyridoxal Schiff base is completely dissolved;
c) adding polyphosphoric acid into the ion mixed solution in which the pyridoxal Schiff base is dissolved, stirring for reaction, cooling after the reaction is finished, and separating out solids from the ion mixed solution; filtering solid particles separated out from the ion mixed solution, wherein the solid obtained by filtering is pyridoxal 5' -phosphate Schiff base, and the obtained liquid is phosphorus-containing ionic liquid; the weight ratio of pyridoxal Schiff base dissolved in the ion mixed solution to the polyphosphoric acid is within the range of 1:1-1:3, the reaction time is within the range of 8-12h, the reaction temperature is within the range of 25-40 ℃, and the temperature is reduced to 10 ℃ after the reaction is finished; the phosphorus-containing ionic liquid obtained by filtering can be recycled;
d) carrying out hydrolysis purification reaction on the pyridoxal 5 '-phosphate Schiff base obtained in the step c) to obtain a final product pyridoxal 5' -phosphate.

Enzyme inhibitor

This vitamin B6-derived coenzyme, often abbreviated PLP, plays a central role in metabolism.
In addition to facilitating aminotransfer reactions, PLP is a coenzyme in reactions involving:
(a) loss of the a-proton, resulting in racemization, cyclization, or b-elimination/replacement (e.g., alanine racemase, 1- aminocyclopropane-1-carboxylate synthase, and serine dehydratase, respectively);
(b) loss of the a-carboxylate as carbon dioxide (e.g., glutamate decarboxylase);
(c) removal/replacement of a group by aldol cleavage (e.g., threonine aldolase);
(d) catalysis via ketimine intermediates (e.g., selenocysteine lyase).

Pyridoxal 5’-Phosphate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Pyridoxal 5’-Phosphate Suppliers

Syntechem Co.,Ltd
Tel
Fax
E-Mail Inquiry
Email
info@syntechem.com
Country
China
ProdList
12984
Advantage
57
Hunan Hui Bai Shi Biotechnology Co., Ltd.
Tel
0731-85526065 13308475853
Email
ivy@hnhbsj.com
Country
China
ProdList
4554
Advantage
62
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12335
Advantage
58
Shanghai T&W Pharmaceutical Co., Ltd.
Tel
+86 21 61551611
Fax
+86 21 50676805
Country
China
ProdList
9891
Advantage
58
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
Advantage
65
Shanghai Yolne Chemical Co., Ltd.
Tel
021-62960152
Fax
021-52212593
Email
934678158@qq.com
Country
China
ProdList
9899
Advantage
55
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4674
Advantage
55
Hunan HuaTeng Pharmaceutical Co., Ltd.,
Tel
400-8592883 15367835770
Fax
0731-82251112
Email
viola@huatengsci.com
Country
China
ProdList
5873
Advantage
58
Suzhou yacoo science co.,Ltd
Tel
0512-87182056 18013166090
Fax
0512-87182056
Email
lingling.qi@yacoo.com.cn
Country
China
ProdList
7295
Advantage
60
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
16166
Advantage
55
More
Less

View Lastest Price from Pyridoxal 5’-Phosphate manufacturers

Hebei Zhuanglai Chemical Trading Co.,Ltd
Product
Pyridoxal 5-Phosphate 853645-22-4
Price
US $120.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20ton
Release date
2024-05-29
Yujiang Chemical (Shandong) Co.,Ltd.
Product
Rubber Accelerator Mbts
Price
US $78.00/kg
Min. Order
1kg
Purity
99.5%
Supply Ability
20T
Release date
2024-05-15
Shanghai Jinli Pharmaceutical Co.,Ltd
Product
pyridoxa 5' phosphate 853645-22-4
Price
US $200.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
60000KG
Release date
2023-01-30

853645-22-4, Pyridoxal 5’-PhosphateRelated Search:


  • Phosphoric acid 2-methyl-3-hydroxy-4-formylpyridine-5-yl ester
  • Pyridoxaol-5-phosphate
  • 3-Hydroxy-2-methyl-5
  • (4-formyl-5-hydroxy-6-methyl-3-pyridinyl)methyl dihydrogen phosphate
  • (4-ForMyl-5-hydroxy-6-Methylpyridin-3-yl)Methyl dihydrogen phosphate
  • PYRIDOXAL 5'-PHOSPHATE HYDRATE POWDE
  • PYRIDOXAL 5'-PHOSPHATE HYDRATE, >=98
  • (4-Formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate hydrate(1:x)
  • PYRIDOXAL-5'-PHOSPHATE
  • PYRIDOXAL-5-PHOSPHATE
  • 3-Hydroxy-2-methyl-5-([phosphonooxy]methyl)-4-pyridinecarboxaldehyde
  • 3-Hydroxy-2-methyl-5-[(phosphonooxy)methyl]-4-pyridinecarboxaldehyde
  • 5-(Phosphonooxy)-3-hydroxy-2-methylpyridine-4-carbaldehyde
  • Pyridoxal-[d3] Phosphate
  • Pyridoxal 5&rsquo
  • -phosphate (hydrate)
  • Pyridoxal 5'-phosphate hydrate powder, BioReagent, suitable for cell culture
  • Pyridoxal-[d3] Phosphate(Vitamin B6-[d3])
  • Pyridoxal 5’-Phosphate ISO 9001:2015 REACH
  • Pyridoxal-5-phosphateQ: What is Pyridoxal-5-phosphate Q: What is the CAS Number of Pyridoxal-5-phosphate Q: What is the storage condition of Pyridoxal-5-phosphate Q: What are the applications of Pyridoxal-5-phosphate
  • rubber accelerator MBTS
  • pyridoxa 5' phosphate
  • Pyridoxal 5'-phosphate hydrate
  • 853645-22-4
  • Other Cofactors
  • Vitamin B
  • Vitamin B6
  • Aldehydes
  • and Substrates
  • Biochemicals and Reagents
  • Building Blocks
  • C8
  • Carbonyl Compounds
  • Chemical Synthesis
  • Cofactors
  • Enzymes
  • Inhibitors
  • Nutrition Research
  • Organic Building Blocks
  • Vitamins