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oleyl acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13533-18-1

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13533-18-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13533-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13533-18:
(7*1)+(6*3)+(5*5)+(4*3)+(3*3)+(2*1)+(1*8)=81
81 % 10 = 1
So 13533-18-1 is a valid CAS Registry Number.
InChI:InChI=1/C21H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23-21(22)4-2/h4,11-12H,2-3,5-10,13-20H2,1H3/b12-11-

13533-18-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name octadec-9-enyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names Oleyl acrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13533-18-1 SDS

13533-18-1Downstream Products

13533-18-1Relevant academic research and scientific papers

Efficient organic solvent and oil sorbent co-polyesters: Poly-9-octadecenylacrylate/methacrylate with 1-hexene

Dutta, Priyanka,Gogoi, Bedanta,Dass, Narendra Nath,Sen Sarma, Neelotpal

, p. 457 - 464 (2013)

In this work, highly absorbent cross linked co-polymer gels of cis-9-octadecen-1-ol with acrylic/methacrylic acid and 1-hexene in different molar ratios were synthesized by thermal polymerization techniques and studied. The polymers were characterized by

Lipid modified spermine derivatives and the use of the derivatives of the prepared liposome

-

Paragraph 0119-0121; 0124-0125, (2017/08/25)

The invention provides a liposome-modified spermine derivative and a liposome prepared by the derivative. The spermine derivative is directly applied or is mixed with one or more selected from cholesterol, neutral lipids and polyethylene glycol (PEG)-modified lipids, which can be adopted as a carrier for entrapping or absorbing bioactive molecular drugs to be loaded into cells. In this way, the effect of regulation, intervention or treatment is realized. In a general formula (1), X1 represents -(CH2)- or carbonyl group, wherein n represents 1, 2 or 3; X2 represents -(CH2)-, ester group, amide group, oxygen, or sulfur; R1 and R2 independently represent C6-C18 alkyl group or lipophilic cholesterol molecules, respectively.

A three-step-one-pot chemo-enzymatic synthesis of epoxyalkanolacylates

Klaas, M. Ruesch,Warwel

, p. 251 - 260 (2007/10/03)

Using the ability of Novozym 435 to catalyze both the perhydrolysis and the interesterification of esters, unsaturated primary alcohols are converted with an ester and hydrogen peroxide to give esters of epoxidized alcohols directly in a convenient three-step-one-pot synthesis with yields of 66-89%.

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