Bis(2-ethylhexyl) maleate

Base Information Edit

Chemical Name:Bis(2-ethylhexyl) maleate
CAS No.:142-16-5
Deprecated CAS:48075-77-0,77666-69-4,77666-69-4
Molecular Formula:C20H36O4
Molecular Weight:340.503
Hs Code.:2917.19 DERIVATION
European Community (EC) Number:205-524-5,946-236-6
NSC Number:345392
UNII:C2F7JHI12L
DSSTox Substance ID:DTXSID2027094
Nikkaji Number:J36.805I
Wikipedia:Bis(2-ethylhexyl)_maleate
Wikidata:Q27275096
ChEMBL ID:CHEMBL1881816
Mol file:142-16-5.mol

Synonyms:Bis(2-ethylhexyl) maleate;142-16-5;Di-2-ethylhexyl maleate;Bis(2-ethylhexyl)maleate;RC Comonomer DOM;Di(2-ethylhexyl) Maleate;Maleic acid, bis(2-ethylhexyl) ester;Di-(2-ethylhexyl)maleate;diethylhexyl maleate;bis(2-ethylhexyl) (Z)-but-2-enedioate;Dioctyl" maleate;2-Butenedioic acid (Z)-, bis(2-ethylhexyl) ester;2-Butenedioic acid (2Z)-, bis(2-ethylhexyl) ester;HSDB 5481;EINECS 205-524-5;UNII-C2F7JHI12L;BRN 1729133;C2F7JHI12L;Bis-(2-ethylhexyl)ester kyseliny maleinove;AI3-07870;DTXSID2027094;Bis-(2-ethylhexyl)ester kyseliny maleinove [Czech];2-Butenedioic acid (2Z)-, 1,4-bis(2-ethylhexyl) ester;EC 205-524-5;DTXCID007094;MFCD00027250;bis(2-ethylhexyl) (2Z)-but-2-enedioate;CAS-142-16-5;4-02-00-02211 (Beilstein Handbook Reference);diethylhexyl malate;DERMOL DOM;Dioctyl Maleate (DOM);bis-2-ethylhexyl maleate;Bis(2 ethylhexyl)maleate;CERAPHYL 45;di-(2-ethylhexyl) maleate;LANOL 84 D;SCHEMBL87501;Maleic acid bis(2-ethylhexyl);CHEMBL1881816;Bis(2-ethylhexyl)-2-butenedioate;Bis(2-ethylhexyl) maleate, 90%;DIETHYLHEXYL MALATE [INCI];DIETHYLHEXYL MALEATE [INCI];Maleic Acid Di(2-ethylhexyl) Ester;Tox21_201422;Tox21_303254;Maleic acid-bis(2-ethylhexyl) ester;NSC345392;AKOS015836338;NSC-345392;DI-2-ETHYLHEXYL MALEATE [HSDB];Bis(2-ethylhexyl) (2Z)-2-butenedioate;NCGC00164190-01;NCGC00164190-02;NCGC00256962-01;NCGC00258973-01;BS-42276;LS-88638;BIS(2-ETHYLHEXYL)MALEATE [USP-RS];M0011;2-Butenedioic acid (z), di-2-ethylhexyl ester;A885223;2-Butenedioic acid, (Z)-, bis(2-ethylhexyl) ester;W-109077;Q27275096;2-BUTANEDIOIC ACID (2Z)-, BIS(2-ETHYLHEXYL) ESTER;Bis(2 ethylhexyl)maleate, Pharmaceutical Secondary Standard;Certified Reference Material;Bis(2-ethylhexyl) maleate, United States Pharmacopeia (USP) Reference Standard

Suppliers and Price of Bis(2-ethylhexyl) maleate

Supply Marketing:Edit

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

TRC
Bis(2 ethylhexyl)maleate
50g
$ 215.00

TCI Chemical
Bis(2-ethylhexyl) Maleate >93.0%(GC)
25mL
$ 24.00

TCI Chemical
Bis(2-ethylhexyl) Maleate >93.0%(GC)
500mL
$ 48.00

Sigma-Aldrich
Bis(2-ethylhexyl) maleate 90%
100ml
$ 47.60

Sigma-Aldrich
Bis(2 ethylhexyl)maleate Pharmaceutical Secondary Standard; Certified Reference Material
2x1g
$ 106.00

Sigma-Aldrich
Bis(2-ethylhexyl) maleate United States Pharmacopeia (USP) Reference Standard
2g
$ 1160.00

Medical Isotopes, Inc.
Bis(2 ethylhexyl)maleate
100 g
$ 800.00

Medical Isotopes, Inc.
Bis(2 ethylhexyl)maleate
50 g
$ 675.00

Matrix Scientific
Bis(2-ethylhexyl) maleate 95+%
5g
$ 908.00

Matrix Scientific
Bis(2-ethylhexyl) maleate 95+%
1g
$ 341.00

Total 106 raw suppliers

Chemical Property of Bis(2-ethylhexyl) maleate Edit

Chemical Property:

Appearance/Colour:Clear to yellow liquid
Vapor Pressure:0Pa at 20℃
Melting Point:-50°C
Refractive Index:1.445 - 1.456
Boiling Point:409.8 °C at 760 mmHg
Flash Point:190.4 °C
PSA：52.60000
Density:0.945 g/cm³
LogP:5.06180
Storage Temp.:Sealed in dry,Room Temperature
Solubility.:Chloroform (Sparingly), Ethyl Acetate(Slightly),Methanol (Slightly)
Water Solubility.:18μg/L at 20℃
XLogP3:6.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:16
Exact Mass:340.26135963
Heavy Atom Count:24
Complexity:329

Purity/Quality:

99% ^*data from raw suppliers

Bis(2 ethylhexyl)maleate ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi,N,Xn
Statements: 36/38-51/53-48/22
Safety Statements: 26-36-61

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Other Classes -> Esters, Other
Canonical SMILES:CCCCC(CC)COC(=O)C=CC(=O)OCC(CC)CCCC
Isomeric SMILES:CCCCC(CC)COC(=O)/C=C\C(=O)OCC(CC)CCCC
Uses Bis(2-ethylhexyl) maleate is a derivative of malic acid, with emollient and skin-conditioning properties. It can also be used as a solvent in cosmetic preparations. It is synthetically manufactured. These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Technology Process of Bis(2-ethylhexyl) maleate

There total 5 articles about Bis(2-ethylhexyl) maleate 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: 100.0%

: 108-31-6
maleic anhydride

: 104-76-7
2-Ethylhexyl alcohol

: 142-16-5,128111-61-5,77666-69-4
bis(2-ethylhexyl) maleate

Guidance literature:: With 3,3′-(2,2-bis(hydroxymethyl)propane-1,3-diyl)bis(1-methyl-1H-imidazol-3-ium) hydrogen sulfate; for 2h; Dean-Stark; Reflux;
DOI:10.1016/j.molliq.2016.11.121