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1,24,25-trihydroxyvitamin D3

Base Information
  • Chemical Name:1,24,25-trihydroxyvitamin D3
  • CAS No.:50648-94-7
  • Molecular Formula:C27H44O4
  • Molecular Weight:432.644
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40432720
  • Mol file:50648-94-7.mol
1,24,25-trihydroxyvitamin D3

Synonyms:1,24,25-trihydroxycholecalciferol;1,24,25-trihydroxyvitamin D3;1,24,25-trihydroxyvitamin D3, (1alpha,3beta,5Z,7E)-isomer;1,24,25-trihydroxyvitamin D3, (1alpha,3beta,5Z,7E,24R)-isomer;1,24,25-trihydroxyvitamin D3, (1alpha,3beta,5Z,7E,24S)-isomer;1,24,25-trihydroxyvitamin D3, (3beta,5Z,7E,24R)-isomer

Suppliers and Price of 1,24,25-trihydroxyvitamin D3
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1,24,25-trihydroxyvitamin D3
Chemical Property:
  • Vapor Pressure:2.6E-17mmHg at 25°C 
  • Boiling Point:607.8°C at 760 mmHg 
  • Flash Point:258.5°C 
  • PSA:80.92000 
  • Density:1.1g/cm3 
  • LogP:4.67550 
  • XLogP3:3.9
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:432.32395988
  • Heavy Atom Count:31
  • Complexity:721
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CCC(C(C)(C)O)O)C1CCC2C1(CCCC2=CC=C3CC(CC(C3=C)O)O)C
  • Isomeric SMILES:C[C@H](CCC(C(C)(C)O)O)[C@H]1CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](C[C@@H](C3=C)O)O)C
Technology Process of 1,24,25-trihydroxyvitamin D3

There total 14 articles about 1,24,25-trihydroxyvitamin D3 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 D-glucose 6-phosphate; bovine adrenodoxin reductase; mouse 25-hydroxyvitamin D3 1α-hydroxylase; mouse adrenodoxin; water; NADPH; glucose 6-phosphate dehydrogenase; at 37 ℃; pH=7.4; Concentration; Kinetics; aq. buffer; phospholipid vesicles; Enzymatic reaction;
DOI:10.1016/j.jsbmb.2010.02.022
Guidance literature:
Multi-step reaction with 2 steps
1: nBu4NF*3H2O / tetrahydrofuran / 22 h
2: AG 50W-X4 resin / methanol / 22 h
With AG 50W-X4 resin; tetrabutyl ammonium fluoride; In tetrahydrofuran; methanol;
DOI:10.1002/1521-3765(20020617)8:12<2747::AID-CHEM2747>3.0.CO;2-J
Guidance literature:
Multi-step reaction with 5 steps
1.1: 89 percent / aq. H2SO4 / acetone / 2.5 h / ultrasonication
2.1: 99 percent / PDC / CH2Cl2 / 6 h
3.1: nBuLi / hexane; tetrahydrofuran / 5 h / -78 - 0 °C
3.2: 92 percent / tetrahydrofuran; hexane / 5 h / 20 °C
4.1: nBu4NF*3H2O / tetrahydrofuran / 22 h
5.1: AG 50W-X4 resin / methanol / 22 h
With dipyridinium dichromate; n-butyllithium; AG 50W-X4 resin; sulfuric acid; tetrabutyl ammonium fluoride; In tetrahydrofuran; methanol; hexane; dichloromethane; acetone; 3.1: Wittig-Horner reaction / 3.2: Wittig-Horner reaction;
DOI:10.1002/1521-3765(20020617)8:12<2747::AID-CHEM2747>3.0.CO;2-J
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