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Pyridoxal 5-Phosphate Monohydrate - 98%, high purity , CAS No.41468-25-1

    Grade & Purity:
  • ≥98%
In stock
Item Number
P110916
Grouped product items
SKU Size
Availability
Price Qty
P110916-1g
1g
10
$17.90
P110916-5g
5g
8
$65.90
P110916-25g
25g
6
$184.90
P110916-100g
100g
2
$663.90
P110916-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$2,985.90

Vitamin B6 metabolite.

Basic Description

Synonyms PLP | P5P | (4-formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate;hydrate | Pyridoxal 5'-phosphate monohydrate | Pyridoxal 5-phosphate monohydrate | (4-Formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate hydrate(1:x) | Tardoxa
Specifications & Purity ≥98%
Biochemical and Physiological Mechanisms Vitamin B6 metabolite that acts as a coenzyme in transamination reactions by forming a Schiff-base linkage with lysine groups on aminotransferase. Also serves as a coenzyme in some decarboxylation and deamination reactions. Can modify lysyl and valyl resi
Storage Temp Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Pyridoxal-5’-phosphate monohydrate is a vitamin B6 metabolite that can modify lysyl and valyl residues in proteins. It has the ability to inhibit purinergic receptors and intracellular influx of Ca2+. Pyridoxal-5’-phosphate monohydrate can modify peptides and suppress their precursor ionization efficiency. Research shows that pyridoxal-5'-phosphate-dependent enzymes can be inhibited by cycloserine.
A vitamin B6 metabolite that can modify lysyl and valyl residues in proteins.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyridines and derivatives
Subclass Pyridine carboxaldehydes
Intermediate Tree Nodes Not available
Direct Parent Pyridoxals and derivatives
Alternative Parents Monoalkyl phosphates  Methylpyridines  Hydroxypyridines  Aryl-aldehydes  Vinylogous acids  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Pyridoxal - Aryl-aldehyde - Monoalkyl phosphate - Hydroxypyridine - Methylpyridine - Organic phosphoric acid derivative - Phosphoric acid ester - Alkyl phosphate - Vinylogous acid - Heteroaromatic compound - Azacycle - Organopnictogen compound - Aldehyde - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as pyridoxals and derivatives. These are compounds containing a pyridoxal moiety, which consists of a pyridine ring substituted at positions 2,3,4, and 5 by a methyl group, a hydroxyl group, a carbaldehyde group, and a hydroxymethyl group, respectively.
External Descriptors Not available

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488183310
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488183310
IUPAC Name (4-formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate;hydrate
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 CC1=NC=C(C(=C1O)C=O)COP(=O)(O)O.O
Isomeric SMILES CC1=NC=C(C(=C1O)C=O)COP(=O)(O)O.O
WGK Germany 2
RTECS UV1208000
Molecular Weight 265.16
Beilstein 234749
Reaxy-Rn 11305661
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11305661&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

24 results found

Lot Number Certificate Type Date Item
D2323271 Certificate of Analysis Jan 06, 2025 P110916
D2323272 Certificate of Analysis Jan 06, 2025 P110916
D2323273 Certificate of Analysis Jan 06, 2025 P110916
D2323276 Certificate of Analysis Jan 06, 2025 P110916
D2323277 Certificate of Analysis Jan 06, 2025 P110916
D2323278 Certificate of Analysis Jan 06, 2025 P110916
D2323270 Certificate of Analysis Jan 06, 2025 P110916
D2323275 Certificate of Analysis Jan 06, 2025 P110916
H2202471 Certificate of Analysis May 07, 2024 P110916
H2202474 Certificate of Analysis May 07, 2024 P110916
G2401135 Certificate of Analysis Apr 01, 2024 P110916
G2401138 Certificate of Analysis Apr 01, 2024 P110916
F2421477 Certificate of Analysis Apr 01, 2024 P110916
C2526541 Certificate of Analysis Apr 01, 2024 P110916
D2508035 Certificate of Analysis Apr 01, 2024 P110916
K2108172 Certificate of Analysis Aug 01, 2023 P110916
K2108173 Certificate of Analysis Aug 01, 2023 P110916
K2108174 Certificate of Analysis Aug 01, 2023 P110916
H2130336 Certificate of Analysis Jun 06, 2023 P110916
H2130282 Certificate of Analysis Jun 06, 2023 P110916
B1805021 Certificate of Analysis Jun 05, 2023 P110916
B1805022 Certificate of Analysis Jun 05, 2023 P110916
A2125163 Certificate of Analysis Dec 06, 2022 P110916
H2202451 Certificate of Analysis Jun 06, 2022 P110916

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Chemical and Physical Properties

Solubility alkaline solutions; sparingly soluble in water
Sensitivity Light & Air Sensitive.
Melt Point(°C) 143 °C
Molecular Weight 265.160 g/mol
XLogP3
Hydrogen Bond Donor Count 4
Hydrogen Bond Acceptor Count 8
Rotatable Bond Count 4
Exact Mass 265.035 Da
Monoisotopic Mass 265.035 Da
Topological Polar Surface Area 118.000 Ų
Heavy Atom Count 17
Formal Charge 0
Complexity 292.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 2

Citations of This Product

1. Liu Jianming, Zhang Han, Xu Yingying, Meng Hao, Zeng An-Ping.  (2023)  Turn air-captured CO2 with methanol into amino acid and pyruvate in an ATP/NAD(P)H-free chemoenzymatic system.  Nature Communications,  14  (1): (1-12). 
2. Junli Guo, Lingling Yang, Huijie Xu, Chenxi Zhao, Zhenqing Dai, Zhida Gao, Yanyan Song.  (2019)  Biomineralization-Driven Ion Gate in TiO2 Nanochannel Arrays for Cell H2S Sensing.  ANALYTICAL CHEMISTRY,  91  (21): (13746–13751). 
3. Chaoqiang Wu, Xin Zhang, Wei Liu, Chengyong Wang, Qianqian Jiang, Feifei Chen, Quanzhen Liu, Fei Cao, Gaowei Zheng, Alei Zhang, Kequan Chen.  (2024)  Biocatalytic Synthesis of Two Furan-Based Amino Compounds 2-Acetyl-4-aminofuran and 3-Acetylamino-5-(α-aminoethyl)-furan from Chitin Resources.  ACS Sustainable Chemistry & Engineering,  12  (30): (11145-11154). 
4. Wang Minyu, Chu Weihua.  (2024)  Dencichine attenuates the virulence of Fusobacterium nucleatum by targeting hydrogen sulfide-producing enzyme.  INTERNATIONAL MICROBIOLOGY,    (1-8). 
5. Kuirong Feng, Lingxin Meng, Jingmei Xu, Pengyun Zhao, Na Li, Jinxuan Lei.  (2024)  Introduction of Bifunctionalized UIO-66-NH2 for Highly Conductive and Long-Term Stable Fluorene-Based Sulfonated Poly(aryl ether ketone sulfone) PEMs.  ACS Applied Polymer Materials,  (17): (10916-10926). 

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