Customization: | Available |
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CAS No.: | 68-94-0 |
Formula: | C5h4n4o |
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Raw Materials Hypoxanthine CAS 68-94-0 98% White Crytalline Powder For Sale
About Hypoxanthine
It is one of the products of the action of xanthine oxidase on xanthine. However, more frequently in purine degradation, xanthine is formed from oxidation of hypoxanthine by xanthine oxidoreductase.
Hypoxanthine-guanine phosphoribosyltransferase converts hypoxanthine into IMP in nucleotide salvage.
Hypoxanthine is also a spontaneous deamination product of adenine. Because of its resemblance to guanine, the spontaneous deamination of adenine can lead to an error in DNA transcription/replication, as it binds with cytosine.
Basic Information
Product Name | Hypoxanthine |
Specification | 98% |
Molecular Formula | C5H4N4O |
Molecular Weight | 136.11 |
CAS No. | 68-94-0 |
Description | White or almost white |
Packing | 25KG/Drum |
Storage | Keep away from sunliht,sealed in dry place. |
Function
Hypoxanthine is a naturally occurring purine derivative. It is occasionally found as a constituent of nucleic acids where it is present in the anticodon of tRNA in the form of its nucleoside inosine. It has a tautomer known as 6-Hydroxypurine.
Hypoxanthine is a necessary additive in certain cell, bacteria, and parasite cultures as a substrate and nitrogen source. For example, it is commonly a required reagent in malaria parasite cultures, since Plasmodium falciparum requires a source of hypoxanthine for nucleic acid synthesis and energy metabolism.
Application
Hypoxanthine is a biological fermentation, and chemical synthesis of nucleoside antiviral drugs is also an intermediate for pharmaceutical raw materials. Used as a raw material for bismuth and azathioprine, and also as an intermediate for the anti-malignant drug 6-Hydrophobic purine.
Packing & Shipment
Quality Control of Health Sources
1) A system in accordance with GMP standard, supervision on whole production process.
2) Health Sources is equipped with advanced detecting device, such as AFS, GC, HPLC, UV etc, supply the
detailed Certificate of Analysis.
3) Procurement-Strictly on selecting raw materials.
4) Production-Strictly according to the standard specifications, conform to USP, EP, BP, CP, AJI, FCC etc
pharmaceutical and/or food standards.
5) Warehousing and storage: Clear and dry condition with suitable temperature.
6) Transportation - Audit and supervise the logistics environment to ensure storage safety.
7) Keep samples for all batches goods to be traceable in case of quality discrepance.
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