Stearyl behenate

Base Information

Chemical Name:Stearyl behenate
CAS No.:24271-12-3
Deprecated CAS:677033-14-6
Molecular Formula:C40H80O2
Molecular Weight:593.074
Hs Code.:2915900090
European Community (EC) Number:246-115-1
UNII:A68S9UI39D
DSSTox Substance ID:DTXSID3066974
Nikkaji Number:J287.198J
Wikidata:Q27273686
RXCUI:1313978
Metabolomics Workbench ID:3705
Mol file:24271-12-3.mol

Synonyms:Stearyl behenate;Octadecyl docosanoate;24271-12-3;Docosanoic acid, octadecyl ester;octadecanyl docosanoate;UNII-A68S9UI39D;A68S9UI39D;EINECS 246-115-1;WE(18:0/22:0);Behenic acid stearyl ester;STEARYLBEHENATE;MFCD00048672;SCHEMBL136531;docosanoic acid octadecyl ester;STEARYL BEHENATE [INCI];DTXSID3066974;Octadecyl docosanoate List Acronyms;BCP32500;LMFA07010060;AKOS037645062;HY-W127424;AS-56718;CS-0185658;FT-0700553;D93433;J-015427;Q27273686

Suppliers and Price of Stearyl behenate

Supply Marketing:

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
STEARYL BEHENATE 95.00%
1G
$ 952.01

Total 13 raw suppliers

Chemical Property of Stearyl behenate

Chemical Property:

Vapor Pressure:7.42E-14mmHg at 25°C
Boiling Point:589.1oC at 760 mmHg
Flash Point:322.8oC
PSA：26.30000
Density:0.856g/cm3
LogP:14.61300
Storage Temp.:2-8°C
XLogP3:19.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:38
Exact Mass:592.61583179
Heavy Atom Count:42
Complexity:488

Purity/Quality:

99.9% ^*data from raw suppliers

STEARYL BEHENATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Esters, Other
Canonical SMILES:CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCC

Technology Process of Stearyl behenate

There total 2 articles about Stearyl behenate 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:

Reference yield: 97.0%

: 112-92-5
1-octadecanol

: 112-85-6
n-docosanoic acid

: 24271-12-3
stearyl behenate

Guidance literature:: With triphenylphosphine-sulfur trioxide adduct; In neat (no solvent); at 110 ℃; for 2h; Green chemistry;
DOI:10.1080/10426507.2020.1845681