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Tocoretinate

Base Information Edit
  • Chemical Name:Tocoretinate
  • CAS No.:40516-48-1
  • Molecular Formula:C49H76O3
  • Molecular Weight:713.141
  • Hs Code.:
  • UNII:0WN694NBMM,CTD060B1SS
  • ChEMBL ID:CHEMBL262520
  • DSSTox Substance ID:DTXSID6046923
  • Metabolomics Workbench ID:70544
  • NCI Thesaurus Code:C66628
  • Nikkaji Number:J378.032E
  • RXCUI:1313259
  • Wikidata:Q27114835
  • Mol file:40516-48-1.mol
Tocoretinate

Synonyms:3,4-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)-2H-1-benzopyran-6-yl-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraenoate;9-cis-tretinoin tocoferil;tocoretinate;tretinoin tocoferil

Suppliers and Price of Tocoretinate
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
  • TRC
  • dl-α-TocopherylRetinoate
  • 10mg
  • $ 55.00
  • American Custom Chemicals Corporation
  • TOCORETINATE 95.00%
  • 250MG
  • $ 730.00
  • American Custom Chemicals Corporation
  • TOCORETINATE 95.00%
  • 500MG
  • $ 1020.00
  • AHH
  • Tocoretinate 98%
  • 1g
  • $ 910.00
Total 45 raw suppliers
Chemical Property of Tocoretinate Edit
Chemical Property:
  • Vapor Pressure:4.49E-23mmHg at 25°C 
  • Boiling Point:761.3°Cat760mmHg 
  • Flash Point:339.8°C 
  • PSA:35.53000 
  • Density:0.959g/cm3 
  • LogP:14.57160 
  • XLogP3:16.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:19
  • Exact Mass:712.57944628
  • Heavy Atom Count:52
  • Complexity:1280
Purity/Quality:

99% *data from raw suppliers

dl-α-TocopherylRetinoate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC(=O)OC2=C(C3=C(C(=C2C)C)OC(CC3)(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C
  • Isomeric SMILES:CC1=C(C(CCC1)(C)C)/C=C/C(=C/C=C/C(=C/C(=O)OC2=C(C3=C(C(=C2C)C)O[C@](CC3)(C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)C)/C)/C
  • Recent EU Clinical Trials:RANDOMIZED PHASE II-STUDY ON VALPROIC ACID, ALL-TRANS RETINOIC ACID AND THEIR COMBINATION IN INDUCTION AND CONSOLIDATION THERAPY AS WELL AS PEGFILGRASTIM AFTER CONSOLIDATION THERAPY IN YOUNGER PATIENTS WITH NEWLY DIAGNOSED ACUTE MYELOID LEUKEMIA
  • Description Tretinoin tocoferil, the a-tocopherol ester of all-trans-retinoic acid, was launched for the treatment of bedsores and skin ulcers such as burn, leg, and diabetic ulcers. It is also an orally active agent for gastric ulcer treatment. Tretinoin tocoferil represents a new class of antiulcer drugs which act by directly promoting tissue repair, distinguished from common drugs that exert an indirect function by suppression of acid-secretion and mucosa protection. The mode of its action has been proposed to relate to its ability to stimulate DNA synthesis of growth-arrested human skin fibroblasts by promoting expression of the epidermal growth factor receptor.
  • Uses dl-α-Tocopheryl Retinoate is an α-tocopherol ester of all-trans retinoic acid (R250200) and is safely used in the treatment of skin ulcer. ?dl-α-Tocopheryl Retinoate inhibited proliferation of human promyelocytic leukemia HL-60 cells and induced granulocytic differentiation of the cells, but to a lesser extent than did retinoic acid.
Technology Process of Tocoretinate

There total 1 articles about Tocoretinate 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:
Refernces Edit
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