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

Encyclopedia

16-Methylheptadecan-1-ol

Base Information Edit
  • Chemical Name:16-Methylheptadecan-1-ol
  • CAS No.:41744-75-6
  • Deprecated CAS:120528-41-8,179607-17-1,59231-38-8,524700-18-3
  • Molecular Formula:C18H38 O
  • Molecular Weight:270.499
  • Hs Code.:2905199090
  • European Community (EC) Number:248-470-8,255-529-1
  • UNII:W29XHH208C
  • DSSTox Substance ID:DTXSID80892268
  • Nikkaji Number:J278.263D
  • Wikidata:Q27158175
  • NCI Thesaurus Code:C174869
  • RXCUI:1362928
  • ChEMBL ID:CHEMBL2107291
  • Mol file:41744-75-6.mol
16-Methylheptadecan-1-ol

Synonyms:isooctadecyl alcohol;isostearyl alcohol

Suppliers and Price of 16-Methylheptadecan-1-ol
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
  • IsostearylAlcoholEX
  • 500mg
  • $ 560.00
Total 3 raw suppliers
Chemical Property of 16-Methylheptadecan-1-ol Edit
Chemical Property:
  • Boiling Point:331.6°Cat760mmHg 
  • Flash Point:124.9°C 
  • PSA:20.23000 
  • Density:0.836g/cm3 
  • LogP:6.09610 
  • XLogP3:8.1
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:15
  • Exact Mass:270.292265831
  • Heavy Atom Count:19
  • Complexity:154
Purity/Quality:

98%Min *data from raw suppliers

IsostearylAlcoholEX *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Chemical Classes:Other Classes -> Alcohols and Polyols, Other
  • Canonical SMILES:CC(C)CCCCCCCCCCCCCCCO
  • Uses Isostearyl Alcohol can be used as reactant/reagent for preparation of organic compounds having linear aliphatic hydrocarbon groups as precipitation accelerators and precipitation methods using them.
Technology Process of 16-Methylheptadecan-1-ol

There total 12 articles about 16-Methylheptadecan-1-ol 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 triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; at 0 - 20 ℃; for 0.75h; Inert atmosphere;
DOI:10.3762/bjoc.9.210
Guidance literature:
With water; toluene-4-sulfonic acid; In methanol; at 50 ℃; for 2h;
Guidance literature:
Multi-step reaction with 3 steps
1: 1.65 g / PPTS / CH2Cl2 / 3 h / 20 °C
2: dilithium tetrachlorocuprate / tetrahydrofuran / -10 - 0 °C
3: 330 mg / p-toluenesulphonic acid monohydrate; water / methanol / 2 h / 50 °C
With dilithium tetrachlorocuprate; water; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; In tetrahydrofuran; methanol; dichloromethane; 1: Addition / 2: coupling / 3: Hydrolysis;
Refernces Edit
Post RFQ for Price