Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

Masoprocol

Base Information Edit
  • Chemical Name:Masoprocol
  • CAS No.:27686-84-6
  • Deprecated CAS:334707-72-1,741285-10-9,1050512-02-1,741285-10-9
  • Molecular Formula:C18H22O4
  • Molecular Weight:302.37
  • Hs Code.:
  • European Community (EC) Number:248-606-6
  • UNII:7BO8G1BYQU
  • DSSTox Substance ID:DTXSID5045178
  • Nikkaji Number:J257.424A
  • Wikipedia:Masoprocol
  • Wikidata:Q6783851
  • NCI Thesaurus Code:C701
  • RXCUI:227239
  • Pharos Ligand ID:NPKM56RHNKN7
  • Metabolomics Workbench ID:42587
  • ChEMBL ID:CHEMBL313972
  • Mol file:27686-84-6.mol
Masoprocol

Synonyms:1,2-Benzenediol,4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (R*,S*)- (9CI);Pyrocatechol, 4,4'-(2,3-dimethyltetramethylene)di-,meso- (8CI);Actinex;CHX 100;Masoprocol;meso-NDGA;meso-Nordihydroguaiareticacid;4-[(2S,3R)-4-(3,4-dihydroxyphenyl)-2,3-dimethylbutyl]benzene-1,2-diol;1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-;4,4'-(2,3-Dimethyl-1,4-butanediyl)bis[1,2-benzenediol];4,4'-(2,3-Dimethylbutane-1,4-diyl)dibenzene-1,2-diol;

Suppliers and Price of Masoprocol
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
  • Crysdot
  • Masoprocol 95+%
  • 1g
  • $ 947.00
  • Biosynth Carbosynth
  • 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (r*,s*)-
  • 25 mg
  • $ 409.00
  • Biosynth Carbosynth
  • 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (r*,s*)-
  • 10 mg
  • $ 205.00
  • Biosynth Carbosynth
  • 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (r*,s*)-
  • 5 mg
  • $ 118.00
  • Biosynth Carbosynth
  • 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (r*,s*)-
  • 2 mg
  • $ 59.00
  • Biosynth Carbosynth
  • 1,2-Benzenediol, 4,4'-(2,3-dimethyl-1,4-butanediyl)bis-, (r*,s*)-
  • 50 mg
  • $ 712.00
  • American Custom Chemicals Corporation
  • MASOPROCOL 95.00%
  • 5G
  • $ 603.00
  • American Custom Chemicals Corporation
  • MASOPROCOL 95.00%
  • 1G
  • $ 468.00
  • American Custom Chemicals Corporation
  • MASOPROCOL 95.00%
  • 500MG
  • $ 434.00
Total 38 raw suppliers
Chemical Property of Masoprocol Edit
Chemical Property:
  • Appearance/Colour:crystals 
  • Vapor Pressure:1.06E-11mmHg at 25°C 
  • Melting Point:185.5°C 
  • Refractive Index:1.626 
  • Boiling Point:526.5 °C at 760 mmHg 
  • Flash Point:247.8 °C 
  • PSA:80.92000 
  • Density:1.241 g/cm3 
  • LogP:3.56640 
  • Storage Temp.:2-8°C 
  • XLogP3:4.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:302.15180918
  • Heavy Atom Count:22
  • Complexity:303
Purity/Quality:

99%, *data from raw suppliers

Masoprocol 95+% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(CC1=CC(=C(C=C1)O)O)C(C)CC2=CC(=C(C=C2)O)O
  • Isomeric SMILES:C[C@H](CC1=CC(=C(C=C1)O)O)[C@@H](C)CC2=CC(=C(C=C2)O)O
  • Recent ClinicalTrials:Pharmacokinetic and Efficacy Study of Nordihydroguaiaretic Acid (NDGA) in Non Metastatic Recurrent Prostate Cancer
  • Description Masoprocol is a lipoxygenase inhibitor launched as a topical agent for the treatment of solar or actinic keratoses. It is the first new topical treatment for pre-malignant skin lesions introduced in twenty years. Masoprocol is obtained from the Larrea tridentata plant and is also under investigation for the treatment of lung, breast, colon and ovarian cancers.
  • Uses Antineoplastic.
Technology Process of Masoprocol

There total 34 articles about Masoprocol 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 hydrogen bromide; In water; at 126 ℃; for 10h; Reagent/catalyst; Inert atmosphere;
Guidance literature:
With hydrogenchloride;
DOI:10.1021/ja01198a513
Guidance literature:
With Larrea divaricata Cav. callus cells; In ethanol; Enzymatic reaction;
DOI:10.1016/j.procbio.2010.08.029
Post RFQ for Price