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guanosine 5'-(tetrahydrogen triphosphate)

Base Information Edit
  • Chemical Name:guanosine 5'-(tetrahydrogen triphosphate)
  • CAS No.:86-01-1
  • Molecular Formula:C10H16 N5 O14 P3
  • Molecular Weight:523.183
  • Hs Code.:
  • Mol file:86-01-1.mol
guanosine 5'-(tetrahydrogen triphosphate)

Synonyms:Guanosinetriphosphate (6CI); 5'-GTP; GTP; Guanosine 5'-triphosphate; Guanosine5'-triphosphoric acid; Guanosine, mono(tetrahydrogen triphosphate) (ester)

Suppliers and Price of guanosine 5'-(tetrahydrogen triphosphate)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • American Custom Chemicals Corporation
  • GTP 95.00%
  • 1G
  • $ 832.18
  • American Custom Chemicals Corporation
  • GTP 95.00%
  • 500MG
  • $ 715.75
  • American Custom Chemicals Corporation
  • GTP 95.00%
  • 250MG
  • $ 664.82
Total 17 raw suppliers
Chemical Property of guanosine 5'-(tetrahydrogen triphosphate) Edit
Chemical Property:
  • Boiling Point:1028.3oC at 760 mmHg 
  • PKA:pK3:3.0(-2);pk5:7.10(-3);pK6:9.3(-4) (25°C,μ=0.1) 
  • Flash Point:575.7oC 
  • PSA:328.53000 
  • Density:2.75g/cm3 
  • LogP:-1.75450 
Purity/Quality:

99%, *data from raw suppliers

GTP 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Guanosine 5''-Triphosphate is used in studying the mechanism of action of selected nucleotide analogs. It is used in the screening or evaluating nucleotide-?based drugs targeting SARS-?CoV-?2 RdRp.
Technology Process of guanosine 5'-(tetrahydrogen triphosphate)

There total 29 articles about guanosine 5'-(tetrahydrogen triphosphate) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With phosphorotriimidazolide; magnesium chloride; at 22 ℃; for 72h; N-ethylmorpholine buffer (pH 7.0);
DOI:10.1016/S0040-4039(00)74092-5
Guidance literature:
With pyridine; water; iodine; In N,N-dimethyl-formamide; at 20 ℃; for 2.25h;
Guidance literature:
With sodium hydroxide; potassium phosphate; nuclease P1; PAN-immobilized PNPase; phospho(enol)pyruvic acid mono potassium salt; magnesium chloride; manganese(ll) chloride; Yield given. Multistep reaction. Yields of byproduct given; 1.) water, 50 deg C, 1 h, 2.) room temperature, 4 days;
DOI:10.1021/ja00339a021
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