Uridine 5'-triphosp...

Uridine 5'-triphosphoric acid trisodium salt CAS 19817-92-6
Uridine 5'-triphosphoric acid trisodium salt CAS 19817-92-6
Uridine 5'-triphosphoric acid trisodium salt CAS 19817-92-6

Uridine 5'-triphosphoric acid trisodium salt CAS 19817-92-6

Min.Order / FOB Price:Get Latest Price

25 Kilogram

FOB Price: USD 200.0000

  • Min.Order :25 Kilogram
  • Purity: ≥98.0%
  • Payment Terms : T/T,,MoneyGram,Other

Keywords

Uridine triphosphoric acid trisodium Uridine 5'-triphosphoric acid trisodium salt 19817-92-6

Quick Details

  • Appearance:White powder
  • Application:Nucleoside
  • PackAge:25kgs/drum paper-drums and two plastic-bags inside
  • ProductionCapacity:2000|Kilogram|Day
  • Storage:Store in tight containers, in a cool dry place
  • Transportation:Express(DHL/FedEx/TNT),AIR,SEA

Superiority:

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Details:

Product Name

 Uridine-5'-triphosphoric acid trisodium salt

Synonyms

 Uridine 5'-triphosphatetrisodium salthydrate;

URIDINE-5'-triphosphate trisodium salt;

Uridine-5'-triphosphoric acid trisodium salt;

Uridine 5'-(disodium dihydrogen triphosphate);

Uridine 5 -Triphosphate TrisodiuM Salt 

CAS

 19817-92-6

Assay

≥98.0

Mol. Formula

 C9H12N2Na3O15P3

Mol. Weight

 550.09

EINECS

 243-347-5

Appearance

White powder

Packing

25kgs/drum (standard packing)

Storage

Tight container, protect from light

Structural formula

 

Function

1. UTP can be used for prevention and treatment of pneumonia, treatment of sinusitis, ciliary dyskinesia, otitis media, bronchitis and other diseases,

2. UTP is a direct precursor of RNA synthesis. It is closely with the carbohydrate metabolism. UTP and 1 - phosphate glucose to generate UDP-glucose and glucose phosphate pyrophosphate catalyzed by enzymes. It is also possible to generate UDP-galactose, UDP-glucose aldehyde acid.

3. UTP can be used as biochemical reagent and intermediate in the production of nucleotide drugs.

 

Quality Standard

Item

Specification

Specific rotation

+39.5 to +41.5°

State of solution(transmittance)

Clear 98.0% min.

Chloride[cl]

0.020% max.

Ammonium [NH4]

0.02% max.

Sulfate[SO4]

0.020% max

Iron[Fe]

10ppm max.

Heavy metals [Pb]

10ppm max

Arsenic[As2O3]

1ppm max

Other amino acids

Chromatographically not detectable

Loss on drying

0.20% max.

Residue on ignition[sulfated]

0.10% max.

Assay

99.0% min

 

 

Shanghai Soyoung Biotechnology Inc. a faithful and professional supplier and exporter of healthcare raw materials for pharmacy, nutrition and food industries for years with own laboratory and GMP standard factories.

Shanghai Soyoung has R&D Center and Testing Center, and has international advanced facilities of HPLC, GC, AAS, UV, TLC, LC-MS and IR equipments. 

Shanghai Soyoung has nearly 20 years production experience, it is producing in GMP workshop, each batch pass strict testing before shipment. Strict quality control is performed in every procedure from material sourcing, processing and testing to packing.

Company name

Shanghai Soyoung Biotechnology Inc.

Main Products

Health care ingredients

Location

Shanghai,China

Business Type

Manufacturer & Trader 

Year start exporting

2011

Number of employees

60-70 people

Factory area

18,000 square meters

Total annual sales volume

US$3,000,000-5,000,000

Main Markets

America,Europe,Mid East,Asia,South Africa and etc.

Certifications

GMP,ISO,HACCP,Kosher

Shanghai SOYOUNG onsite assessment conducted by Bureau Veritas commissioned at June 2018. Assessed Supplier of Shanghai SOYOUNG is a faithful and professional supplier of health raw materials in pharmacy, food, cosmetic and other fields for many years, with own laboratories and GMP standard factories.

1. 12 years specialized in health products field.
2. GMP/ISO certificated factories and stable supply chain.
3. Quality first, strictly control before shipments.
4. Custom synthesis by more than 20 professional chemists.
5. Small order,free sample and one step service available.
6. Rapid delivery, 1-6 business days from China warehouse.
7. Support 7 days refund money in case delay shipment.
8. Assessment conducted by Bureau Veritas at 2018.

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