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2915-53-9

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2915-53-9 Usage

Uses

dioctyl maleate is a film former and emollient derived from maleic acid.

Check Digit Verification of cas no

The CAS Registry Mumber 2915-53-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2915-53:
(6*2)+(5*9)+(4*1)+(3*5)+(2*5)+(1*3)=89
89 % 10 = 9
So 2915-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H36O4/c1-3-5-7-9-11-13-17-23-19(21)15-16-20(22)24-18-14-12-10-8-6-4-2/h15-16H,3-14,17-18H2,1-2H3/b16-15-

2915-53-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dioctyl (Z)-but-2-enedioate

1.2 Other means of identification

Product number -
Other names dicapryl maleate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Surface active agents
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:2915-53-9 SDS

2915-53-9Relevant articles and documents

Porous polymer oil sorbents based on PET fibers with crosslinked copolymer coatings

Atta, Ayman M.,Brostow, Witold,Hagg Lobland, Haley E.,Hasan, Abdul-Raheim M.,Perez, Jose M.

, p. 25849 - 25857 (2013/12/04)

Oil sorbents - namely materials that can be used to extract oil after a spill - were fabricated from non-woven polyethylene terephthalate (NWPET) fibers modified by the adherence of crosslinked polymer coatings to the fiber surface. The NWPET fibers, which serve as a structural support for the applied functional coatings, were produced from recycled PET (polyethylene terephthalate) bottles. The oil absorbing coatings were comprised of crosslinked homopolymers and copolymers based on octadecyl acrylate (ODA), maleic anhydride (MA), and related esters of MA. The crosslinked polymer networks were synthesized by both suspension and bulk polymerization techniques using divinylbenzene (DVB) as the crosslinking agent. Efficacy of the coated NWPET fibers as oil sorbers was determined by oil absorption tests in toluene and in 10% crude oil in toluene. Rigidity, porosity and swelling of the crosslinked polymers were evaluated and correlated to the chemical structures, composition, and reaction media. Suspension polymerization yielded the desired morphology and function, providing higher porosity and in consequence a high absorption capacity.

Role of the succinate skeleton in the disorder-order transition of AOT and its analogous molecules: Detection by infrared absorption spectra of the configurations arising from the difference in torsion angles of the succinate skeleton

Okabayashi, Hiro-Fumi,Izawa, Ken-Ichi,Sumiya, Akiko,Eastoe, Julian,O'Connor, Charmian J.

experimental part, p. 651 - 659 (2010/08/08)

The IR spectra in the 13001450 cm-1 region, which reflect the CH and CH2 deformation vibrational modes of the succinate skeleton, have been investigated in detail for sodium dialkylsulfonates (alkyl groups: Ethyl, n-propyl, n-butyl, n-hexyl, n-heptyl, n-octyl, n-decyl, and n-dodecyl) and sodium 1,2-bis(2-ethylhexyl)sulfosuccinate (sodium 1,2-bis(2- ethylhexyloxycarbonyl)ethanesulfonate) (AOT). The results have provided clear evidence that two configurations, arising from the difference in the torsion angles of the succinate skeleton, are preferentially stabilized in aqueous solution as well as in the solid state, depending upon the concentration. Thus, the IR spectra of this region can be used as a powerful tool for elucidation of the mechanism of the disorderorder transition in aggregate systems of AOT or its homologs at the molecular level.

Solubilities of AOT analogues surfactants in supercritical CO2 and HFC-134a fluids

Liu, Zhao-Tie,Wu, Jin,Liu, Ling,Sun, Changan,Song, Liping,Gao, Ziwei,Dong, Wensheng,Lu, Jian

, p. 1761 - 1768 (2007/10/03)

A series of sodium bis(2-ethylhexyl) sulfosuccinate (AOT) analogue surfactants [sodium dibutyl sulfosuccinate (DBSS), sodium dipentyl sulfosuccinate (DPSS), sodium dihexyl sulfosuccinate (DHSS), and sodium dioctyl sulfosuccinate (DOSS)] were synthesized and characterized with 1H NMR and elemental analysis. The solubilities of surfactants in supercritical CO2 (scCO2) and supercritical 1,1,1,2-tetrafluoroethane (HFC-134a) fluids at a temperature range from (308 to 338) K and under pressures of (10 to 30) MPa were measured using a static method coupled with gravimetric analysis. The solubilities of these surfactants are much higher in HFC-134a fluid as compared with that in scCO2. The solubilities increased with increasing temperature and pressure for both scCO2 and HFC-134a fluids. The solubilities in scCO2 increased with increasing carbon atom number of surfactant, whereas they decreased with increasing carbon atom number of surfactant in HFC-134a. The density of scCO2 was simulated with the Peng-Robinson (P-R) equation. The experimental data were used to validate the accuracy of the P-R equation.

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