Retinol oleate

Base Information

Chemical Name:Retinol oleate
CAS No.:631-88-9
Molecular Formula:C38H62 O2
Molecular Weight:550.909
Hs Code.:
UNII:8HU01DH65P
DSSTox Substance ID:DTXSID601021962
Metabolomics Workbench ID:65240
Nikkaji Number:J676.472J
Wikidata:Q27139070
Mol file:631-88-9.mol

Synonyms:retinol oleate;retinyl oleate

Suppliers and Price of Retinol oleate

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

Usbiological
all-trans-Retinyl Oleate
100mg
$ 460.00

Medical Isotopes, Inc.
all-trans-RetinylOleate
1 g
$ 2200.00

Medical Isotopes, Inc.
all-trans-RetinylOleate
100 mg
$ 650.00

Total 4 raw suppliers

Chemical Property of Retinol oleate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:631.644°C at 760 mmHg
Flash Point:75.728°C
PSA：26.30000
Density:0.923g/cm³
LogP:12.09870
Storage Temp.:Amber Vial, -86°C Freezer, Under inert atmosphere
Solubility.:Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
XLogP3:13.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:22
Exact Mass:550.47498122
Heavy Atom Count:40
Complexity:875

Purity/Quality:

99% ^*data from raw suppliers

all-trans-Retinyl Oleate ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCC=CCCCCCCCC(=O)OCC=C(C)C=CC=C(C)C=CC1=C(CCCC1(C)C)C
Isomeric SMILES:CCCCCCCC/C=C\CCCCCCCC(=O)OC/C=C(\C)/C=C/C=C(\C)/C=C/C1=C(CCCC1(C)C)C
Uses retinol oleate is used for the preparation of oil-based composition for acne treatment. all-trans-Retinyl Oleate is used for the preparation of oil-based composition for acne treatment.

Technology Process of Retinol oleate

There total 3 articles about Retinol oleate 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: 69.0%

: 112-80-1,2027-47-6
cis-Octadecenoic acid

: 127-47-9,64536-04-5
Retinol acetate

: 631-88-9,79433-57-1
retinyl stearate

: 68-26-8
RETINOL

Guidance literature:: With Novozyme 435 (from Candida antarctica immobilized on acrylic resin); Amberlyst A-21; In toluene; at 20 ℃; for 15h; Product distribution / selectivity; Enzymatic reaction;

Reference yield:

: 112-80-1,2027-47-6
cis-Octadecenoic acid

: 127-47-9,64536-04-5
Retinol acetate

: 631-88-9,79433-57-1
retinyl stearate

Guidance literature:: With novozyme 435; In toluene; at 20 ℃; for 20h; Schlenk technique; Inert atmosphere; Enzymatic reaction;
DOI:10.1194/jlr.D040204