Glyceryl 1-undecylenate

Base Information

Chemical Name:Glyceryl 1-undecylenate
CAS No.:62285-15-8
Molecular Formula:C14H26O4
Molecular Weight:
Hs Code.:
UNII:B68LJT9544
DSSTox Substance ID:DTXSID10432858
Nikkaji Number:J501.840D
Wikidata:Q27274427
RXCUI:1607316

Synonyms:Glyceryl 1-undecylenate;1-Monoundecenoin;Undecenoin, 1-mono-;62285-15-8;Glyceryl undecylenate [INCI];10-Undecenoic acid, 2,3-dihydroxypropyl ester;2,3-Dihydroxypropyl 10-undecenoate;2,3-dihydroxypropyl Undec-10-enoate;UNII-B68LJT9544;B68LJT9544;1-Monoundec-10-enoin;SCHEMBL33815;DTXSID10432858;Q27274427

Suppliers and Price of Glyceryl 1-undecylenate

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

Total 12 raw suppliers

Chemical Property of Glyceryl 1-undecylenate

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:13
Exact Mass:258.18310931
Heavy Atom Count:18
Complexity:216

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCCCCCCCCC(=O)OCC(CO)O
General Description **10-Undecenoic acid, 2,3-dihydroxypropyl ester** (also known as glycerol monoundecylenate or monoglyceride of undecylenic acid) is a bio-based monoglyceride derived from the condensation of undecylenic acid with glycerol or its derivatives. It serves as a precursor for synthesizing photopolymerizable monomers, such as diacrylated or dimethacrylated derivatives, which can be cross-linked under UV radiation to form polymeric materials with applications in coatings or surface modifications. Additionally, this monoglyceride can be used to functionalize porous silicon surfaces, enhancing hydrophilicity and stability. 10-Undecenoic acid, 2,3-dihydroxypropyl ester is characterized by its polar head group and fatty acid chain, making it suitable for both material science and surface chemistry applications. **Other names:** Glycerol monoundecylenate, Monoundecylenin, 2,3-Dihydroxypropyl undec-10-enoate.

Technology Process of Glyceryl 1-undecylenate

There total 5 articles about Glyceryl 1-undecylenate 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: 85.0%

: 112-38-9
10-undecenoic acid

: 556-52-5
oxiranyl-methanol

: 62285-15-8
2,3-dihydroxypropyl undec-10-enoate

Guidance literature:: With (4-aminobutyl)silyl-MCM-41 type silica; In toluene; at 79.9 ℃; for 24h;
DOI:10.1021/jo9614001

Reference yield: 84.0%

: 143-07-7
lauric acid

: 931-40-8
4-hydroxymethyl-1,3-dioxolan-2-one

: 62285-15-8
2,3-dihydroxypropyl undec-10-enoate

Guidance literature:: With tetra-(n-butyl)ammonium iodide; at 140 - 142 ℃; for 24h; Reflux;
DOI:10.1007/s11746-013-2375-0

Reference yield: 75.0%

: 142564-38-3
(2-Dec-9-enyl-[1,3]dioxolan-4-yl)-methanol

: 62285-15-8
2,3-dihydroxypropyl undec-10-enoate

: 142564-41-8
β-glycerol monoundecenoate

Guidance literature:: With tert.-butylhydroperoxide; dipyridinium dichromate; In dichloromethane; for 6h; Yields of byproduct given; Ambient temperature;
DOI:10.1021/jo00044a042