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19817-92-6

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19817-92-6 Usage

Description

Uridine-5'-triphosphoric acid trisodium salt, also known as UTP, is a polyphosphate analogue of uridine that is used in the synthesis of agonists at the G-protein-coupled P2Y receptors.

Chemical Properties

White crystalline powder

Uses

Different sources of media describe the Uses of 19817-92-6 differently. You can refer to the following data:
1. psychostimulant
2. Uridine-5'-triphosphoric acid trisodium salt is a polyphosphate analogue of the nucleoside uridine used in the preparation of potent and selective agonists at the G-protein-coupled P2Y receptors.
3. P2Y receptor agonist.

Biochem/physiol Actions

Uridine-5′-Triphosphate?(UTP) is a cytosolic nucleotide component of nucleic acids. It serves as a signaling molecule in the extracellular space. Uridine-5′-Triphosphate?(UTP) is involved in various pathophysiological responses in the nervous system.?UTP also plays a major role in the regeneration process.

Check Digit Verification of cas no

The CAS Registry Mumber 19817-92-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19817-92:
(7*1)+(6*9)+(5*8)+(4*1)+(3*7)+(2*9)+(1*2)=146
146 % 10 = 6
So 19817-92-6 is a valid CAS Registry Number.

19817-92-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (U0022)  Uridine 5'-Triphosphate Trisodium Salt Hydrate  >95.0%(HPLC)

  • 19817-92-6

  • 100mg

  • 415.00CNY

  • Detail
  • Sigma

  • (U6625)  Uridine5′-triphosphatetrisodiumsalthydrate  from yeast, Type III, ≥96%

  • 19817-92-6

  • U6625-25MG

  • 307.71CNY

  • Detail
  • Sigma

  • (U6625)  Uridine5′-triphosphatetrisodiumsalthydrate  from yeast, Type III, ≥96%

  • 19817-92-6

  • U6625-100MG

  • 1,031.94CNY

  • Detail
  • Sigma

  • (U6625)  Uridine5′-triphosphatetrisodiumsalthydrate  from yeast, Type III, ≥96%

  • 19817-92-6

  • U6625-500MG

  • 3,329.82CNY

  • Detail
  • Sigma

  • (U6625)  Uridine5′-triphosphatetrisodiumsalthydrate  from yeast, Type III, ≥96%

  • 19817-92-6

  • U6625-1G

  • 5,733.00CNY

  • Detail
  • Sigma

  • (U6750)  Uridine5′-triphosphatetrisodiumsalthydrate  Type IV, 90-95%

  • 19817-92-6

  • U6750-100MG

  • 499.59CNY

  • Detail
  • Sigma

  • (U6750)  Uridine5′-triphosphatetrisodiumsalthydrate  Type IV, 90-95%

  • 19817-92-6

  • U6750-250MG

  • 833.04CNY

  • Detail
  • Sigma

  • (U6750)  Uridine5′-triphosphatetrisodiumsalthydrate  Type IV, 90-95%

  • 19817-92-6

  • U6750-500MG

  • 1,443.78CNY

  • Detail
  • Sigma

  • (U6750)  Uridine5′-triphosphatetrisodiumsalthydrate  Type IV, 90-95%

  • 19817-92-6

  • U6750-1G

  • 2,521.35CNY

  • Detail

19817-92-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Uridine-5'-triphosphoric acid trisodium salt

1.2 Other means of identification

Product number -
Other names UTP trisodium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19817-92-6 SDS

19817-92-6Relevant articles and documents

Sulfonyl imidazolium salts as reagents for the rapid and efficient synthesis of nucleoside polyphosphates and their conjugates

Mohamady, Samy,Desoky, Ahmed,Taylor, Scott D.

, p. 402 - 405 (2012/02/16)

A procedure for the synthesis of nucleoside polyphosphates and their conjugates using sulfonylimidazolium salts as key reagents is described. The procedure is rapid and high yielding, does not require prior protection and subsequent deprotection of the donors or acceptors, and can be used to activate nucleoside mono-, di- and triphosphates, and a wide variety of acceptors and donors can be used.

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