PRODUCTS

DI(2-ETHYLHEXYL) MALEATE

Di(2-ethylhexyl) Maleate can also be used as a solvent in cosmetic preparations.
Di(2-ethylhexyl) Maleate is used as a green plasticizer in variety of applications such as adhesives and coatings.
Di(2-ethylhexyl) Maleate is used in the following products: adhesives and sealants, heat transfer fluids, hydraulic fluids, perfumes and fragrances and cosmetics and personal care products.

CAS Number: 142‑16‑5
EC Number: 205‑524‑5
MDL Number: MFCD00027250
IUPAC Name: Bis(2‑ethylhexyl) (2 Z)‑but‑2‑enedioate
Molecular Formula: C₂₀H₃₆O₄
Molecular Weight: ~340.50 g/mol

SYNONYMS:
2-Butenedioic acid (Z)-, bis(2-ethylhexyl) ester, Maleic acid, bis(2-ethylhexyl) ester, Bis-(2-ethylhexyl)ester kyseliny maleinove, Di-(2-ethylhexyl)maleate, DOM, RC Comonomer DOM, Bis(2-ethylhexyl) (2Z)-2-butenedioate, 2-Butenedioic acid (Z), di-2-ethylhexyl ester, 2-Butenedioic acid (2Z)-, 1,4-bis(2-ethylhexyl) ester, 2-Butenedioic acid (2Z)-, bis(2-ethylhexyl) ester, DOM, DICAPRYLYL MALEATE, DIETHYLHEXYL MALEATE, WS4, PCWH, WS2E, WS4C, α-Bulnesene, rccomonomerdom, Rc comonomer dom, Bis(2-ethylhexyl) (2Z)-2-butenedioate, bis(2-ethylhexyl)-2butenedioate , bis(2-ethylhexyl)-2-butenedioate , Bis-(2-ethylhexyl)ester kyseliny maleinove, bis-(2-ethylhexyl)esterkyselinymaleinove , di(2-ethvlhexvl)maleate , Rc comonomer dom, rccomonomerdom, Bis(2-ethylhexyl) (2Z)-but-2-enedioate, Bis(2-ethylhexyl) maleate, Di-2-ethylhexyl maleate, Diethylhexyl maleate, DOM, "Dioctyl" maleate, 2-Butenedioic acid (Z)-, bis(2-ethylhexyl) ester, Bis(2-ethylhexyl) maleate, Bis(2-ethylhexyl)maleate, Bis-(2-ethylhexyl)ester kyseliny maleinove [Czech], Di-(2-ethylhexyl)maleate, Maleic acid, bis(2-ethylhexyl) ester, RC Comonomer DOM, [ChemIDplus]
Bis(2-ethylhexyl) maleate, Di-2-ethylhexyl maleate, Dioctyl maleate, Bis(2-ethylhexyl) maleate, Di-2-ethylhexyl maleate, Dioctyl maleate, 2-Butenedioic Acid (2Z)-Bis(2-ethylhexyl) Ester, 2-Butenedioic Acid (Z)-Bis(2-ethylhexyl) Ester, (USP), bis 2-ethylhexyl maleate, di-2-ethylhexyl maleate, rc comonomer dom, di 2-ethylhexyl maleate, maleic acid, bis 2-ethylhexyl ester, 2-butenedioic acid 2z-, bis 2-ethylhexyl ester, maleic acid dioctyl ester, 2-butenedioic acid z-, bis 2-ethylhexyl ester, (Di(2‑ethylhexyl) Maleate, Dioctyl Maleate, Maleic Acid Di(2‑ethylhexyl) Ester, Maleic Acid Dioctyl Ester, Di‑2‑ethylhexyl maleate, 2‑Butenedioic acid (Z)‑bis(2‑ethylhexyl) ester, DOM), Bis(2-ethylhexyl) maleate, 142-16-5, Bis(2-ethylhexyl)maleate, Di-2-ethylhexyl maleate, RC Comonomer DOM, diethylhexyl maleate, Di-(2-ethylhexyl)maleate, Maleic acid, bis(2-ethylhexyl) ester, bis(2-ethylhexyl) (Z)-but-2-enedioate, HSDB 5481, 2-Butenedioic acid (Z)-, bis(2-ethylhexyl) ester, 2-Butenedioic acid (2Z)-, bis(2-ethylhexyl) ester, diethylhexyl malate, EINECS 205-524-5, C2F7JHI12L, BRN 1729133, DTXSID2027094, DERMOL DOM, AI3-07870, Bis-(2-ethylhexyl)ester kyseliny maleinove, CERAPHYL 45, Bis-(2-ethylhexyl)ester kyseliny maleinove [Czech], LANOL 84 D, 2-Butenedioic acid (2Z)-, 1,4-bis(2-ethylhexyl) ester, DTXCID007094, EC 205-524-5, DI-2-ETHYLHEXYL MALEATE [HSDB], BIS(2-ETHYLHEXYL)MALEATE [USP-RS], Dioctyl" maleate, 2-BUTANEDIOIC ACID (2Z)-, BIS(2-ETHYLHEXYL) ESTER, BIS(2-ETHYLHEXYL)MALEATE (USP-RS), Di(2ethylhexyl)maleate, Bis(2ethylhexyl)maleate, Bis(2ethylhexyl) maleate, DIETHYLHEXYL MALATE [INCI], DIETHYLHEXYL MALEATE [INCI], Maleic acid, bis(2ethylhexyl) ester, Bis(2ethylhexyl)ester kyseliny maleinove, 2Butenedioic acid (Z), bis(2ethylhexyl) ester, 205-524-5, 946-236-6, Di(2-ethylhexyl) Maleate, MFCD00027250, bis(2-ethylhexyl) (2Z)-but-2-enedioate, CAS-142-16-5, 4-02-00-02211 (Beilstein Handbook Reference), UNII-C2F7JHI12L, Bis(2 ethylhexyl)maleate, Maleic Acid Dioctyl Ester, di-(2-ethylhexyl) maleate, SCHEMBL87501, CHEMBL1881816, Bis(2-ethylhexyl) maleate, 90%, Maleic Acid Di(2-ethylhexyl) Ester, Tox21_201422, Tox21_303254, Maleic acid-bis(2-ethylhexyl) ester, NSC345392, SBB060328, AKOS015836338, FB62553, NSC-345392, Bis(2-ethylhexyl) (2Z)-2-butenedioate, NCGC00164190-01, NCGC00164190-02, NCGC00256962-01, NCGC00258973-01, BS-42276, Di(2-ethylhexyl) Maleate;Dioctyl Maleate, di2-ethylhexyl (2Z)but-2-ene-1,4-dioate, CS-0152377, M0011, NS00003256, 2-Butenedioic acid (z), di-2-ethylhexyl ester, Q27275096, Bis(2 ethylhexyl)maleate, Pharmaceutical Secondary Standard; Certified Reference Material, Bis(2-ethylhexyl) maleate, United States Pharmacopeia (USP) Reference Standard, 2-Butenedioic acid (Z)-, bis(2-ethylhexyl) ester, Maleic acid, bis(2-ethylhexyl) ester, Bis-(2-ethylhexyl)ester kyseliny maleinove, Di-(2-ethylhexyl)maleate, DOM, RC Comonomer DOM, Bis(2-ethylhexyl) (2Z)-2-butenedioate, 2-Butenedioic acid (Z), di-2-ethylhexyl ester, 2-Butenedioic acid (2Z)-, 1,4-bis(2-ethylhexyl) ester, 2-Butenedioic acid (2Z)-, bis(2-ethylhexyl) ester, 2- butenedioic acid (2Z)-, bis(2-ethylhexyl) ester, 2- butenedioic acid (Z)-, bis(2-ethylhexyl) ester, 2- butenedioic acid, bis(2-ethylhexyl) ester, (2Z)-, dermol DOM, di-(2-ethylhexyl)maleate, di-2-ethylhexyl maleate, di(2-ethylhexyl) maleate, di2-ethylhexyl (2Z)but-2-ene-1,4-dioate, dioctyl maleate (so called), 2- ethylhexyl maleate, bis(2- ethylhexyl) (2Z)-2-butenedioate, bis(2- ethylhexyl) (2Z)-but-2-enedioate, bis(2- ethylhexyl) (Z)-but-2-enedioate, bis(2- ethylhexyl) maleate, bis(2- ethylhexyl)maleate, hallstar DOM, maleic acid di(2-ethylhexyl) ester, maleic acid dioctyl ester, maleic acid, bis(2-ethylhexyl) ester, RC comonomer DOM

Di(2-ethylhexyl) Maleate is a potential anti-inflammatory and antimicrobial agent, extracted from Urtica dioica L. (Urticaceae) leaves.
Di(2-ethylhexyl) Maleate (C₂₀H₃₆O₄) is a carboxylic acid derivative and an organic ester.
Di(2-ethylhexyl) Maleate appears at room temperature as a colorless to slightly yellowish liquid with a mild, characteristic odor.

Di(2-ethylhexyl) Maleate is typically viscous in consistency and exhibits low volatility under standard atmospheric conditions.
Due to its ester functional groups, Di(2-ethylhexyl) Maleate demonstrates limited solubility in water but is miscible with many common organic solvents such as alcohols, ethers, and hydrocarbons.

Di(2-ethylhexyl) Maleate was first synthesized in the mid-20th century during investigations into plasticizers and polymer modifiers.
Di(2-ethylhexyl) Maleate is commonly prepared via the esterification of maleic acid with 2-ethylhexanol under acidic catalytic conditions, often using sulfuric acid or solid acid catalysts to facilitate the condensation reaction while removing water azeotropically.

Di(2-ethylhexyl) Maleate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 to < 10 000 tonnes per annum.
Di(2-ethylhexyl) Maleate is a fatty acid that is used in pharmaceutical preparations as a basic structure.

Di(2-ethylhexyl) Maleate has a reactive hydroxyl group and can be used as a chemical species.
Di(2-ethylhexyl) Maleate is an alkanoic acid that can be converted to maleic acid by reacting with water vapor.
This conversion increases the reactivity of the hydroxyl group, which makes Di(2-ethylhexyl) Maleate useful for reactions with other chemicals.

Di(2-ethylhexyl) Maleate also reacts with calcium stearate to form dimethyl fumarate, which is used in the production of polycarboxylic acids.
Di(2-ethylhexyl) Maleate is a chemical compound that functions as a plasticizer in experimental applications.

Di(2-ethylhexyl) Maleate interacts at the molecular level by forming strong, flexible bonds with polymer chains, thereby increasing the flexibility and durability of plastic materials.
Di(2-ethylhexyl) Maleate acts by reducing the intermolecular forces between polymer chains, allowing them to slide past one another more easily.

This results in improved flexibility and resistance to breaking or cracking in plastic products.
Di(2-ethylhexyl) Maleate achieves this by effectively lubricating the polymer chains, enhancing their ability to move and bend without becoming brittle.

For safe storage, Di(2-ethylhexyl) Maleate should be kept in tightly sealed containers in a cool, well-ventilated area, away from strong oxidizing agents and heat sources.
Di(2-ethylhexyl) Maleate is a derivative of malic acid, with emollient and skin-conditioning properties.

Di(2-ethylhexyl) Maleate can also be used as a solvent in cosmetic preparations.
Di(2-ethylhexyl) Maleate is synthetically manufactured.

Di(2-ethylhexyl) Maleate is the chemical compound with the structural formula (H3C(−CH2)3−CH(−CH2−CH3)−CH2−O−C(=O)−CH=)2, where the two carboxylate groups are mutually cis.
Di(2-ethylhexyl) Maleate can be described as the double ester of maleic acid with the alcohol 2-ethylhexanol.

Di(2-ethylhexyl) Maleate is commonly called dioctyl maleate (DOM), reflecting the older usage of "octane" to refer to any 8-carbon alkane, straight-chained or branched.
Di(2-ethylhexyl) Maleate is manufactured by treating 2-ethylhexanol with maleic anhydride and an esterification catalyst.

Di(2-ethylhexyl) Maleate is a key intermediate raw material in the production of dioctyl sulfosuccinate (DOSS, docusate) salts, used medically as laxatives and stool softeners, and in many other applications as versatile surfactants
Di(2-ethylhexyl) Maleate is a chemical compound from the group of carboxylic acid esters .

Di(2-ethylhexyl) Maleate is a liquid between -60 and 164∘C(boiling point at 10 mmHg).
Di(2-ethylhexyl) Maleate is a derivative of malic acid, with emollient and skin-conditioning properties.
Di(2-ethylhexyl) Maleate is synthetically manufactured.

Di(2-ethylhexyl) Maleate is an aliphatic ester which is prepared by catalytic esterification of maleic acid and 2-ethylhexyl alcohol.
General description Di(2-ethylhexyl) Maleate is an aliphatic ester which is prepared by catalytic esterification of maleic acid and 2-ethylhexyl alcohol.

USES and APPLICATIONS of DI(2-ETHYLHEXYL) MALEATE:
Di(2-ethylhexyl) Maleate is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Di(2-ethylhexyl) Maleate can also be used as a solvent in cosmetic preparations.

Di(2-ethylhexyl) Maleate is used as a green plasticizer in variety of applications such as adhesives and coatings.
Di(2-ethylhexyl) Maleate is used in the following products: adhesives and sealants, heat transfer fluids, hydraulic fluids, perfumes and fragrances and cosmetics and personal care products.

Other release to the environment of Di(2-ethylhexyl) Maleate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).
Release to the environment of Di(2-ethylhexyl) Maleate can occur from industrial use: industrial abrasion processing with low release rate (e.g. cutting of textile, cutting, machining or grinding of metal).

Di(2-ethylhexyl) Maleate is a key intermediate raw material in the production of dioctyl sulfosuccinate (DOSS, docusate) salts, used medically as laxatives and stool softeners, and in many other applications as versatile surfactants.
Di(2-ethylhexyl) Maleate is used as a comonomer and internal plasticizer with vinyl acetate, acrylates, methacrylates, and n-vinyl-n-methylacetamide.

Di(2-ethylhexyl) Maleate is also used to make sulfosuccinate anionic surfactants.
Di(2-ethylhexyl) Maleate is used in paints, lacquers, varnishes, textiles, and adhesives.

Other release to the environment of Di(2-ethylhexyl) Maleate is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

Di(2-ethylhexyl) Maleate can be found in complex articles, with no release intended: vehicles.
Di(2-ethylhexyl) Maleate can be found in products with material based on: plastic (e.g. food packaging and storage, toys, mobile phones), rubber used for large surface area articles (e.g. construction and building materials for flooring) and plastic used for large surface area articles (e.g. construction and building materials for flooring, insulation).

Di(2-ethylhexyl) Maleate is widely used as a plasticizer and comonomer, particularly in adhesives, coatings, films, rubbers, and polymers like vinyl acetate and acrylics.
Di(2-ethylhexyl) Maleate provides flexibility, transparency, and impact resistance in polymer materials.

Di(2-ethylhexyl) Maleate is employed as a green alternative to phthalate-based plasticizers in sustainable formulations.
Di(2-ethylhexyl) Maleate is used in the following products: adhesives and sealants, coating products and hydraulic fluids.
Di(2-ethylhexyl) Maleate is used for the manufacture of: rubber products and plastic products.

Other release to the environment of Di(2-ethylhexyl) Maleate is likely to occur from: indoor use as processing aid.
Di(2-ethylhexyl) Maleate is used in the following products: inks and toners.
Release to the environment of Di(2-ethylhexyl) Maleate can occur from industrial use: formulation of mixtures.

Di(2-ethylhexyl) Maleate is used as a plasticizer in a variety of applications such as adhesives and coatings.
Di(2-ethylhexyl) Maleate is also used as a comonomer and plasticizer in the production of vinyl acetate , acrylates , and methacrylates
Di(2-ethylhexyl) Maleate is used in the following products: adhesives and sealants.

Di(2-ethylhexyl) Maleate has an industrial use resulting in manufacture of another substance (use of intermediates).
Di(2-ethylhexyl) Maleate is used for the manufacture of: chemicals.
Release to the environment of Di(2-ethylhexyl) Maleate can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates), for thermoplastic manufacture and in the production of articles.

Release to the environment of Di(2-ethylhexyl) Maleate can occur from industrial use: manufacturing of the substance.
Di(2-ethylhexyl) Maleate is also used as a solid catalyst for polymerization reactions and has been shown to be useful for particle synthesis.
Di(2-ethylhexyl) Maleate is also used in the preparation of lubricants additives.

Di(2-ethylhexyl) Maleate is suitable for scientific research.
In experimental applications, Di(2-ethylhexyl) Maleate′s mechanism of action involves enhancing the performance and longevity of plastic materials by modifying their physical properties.

Di(2-ethylhexyl) Maleate's function as a plasticizer allows for the development of more flexible and durable plastic products without compromising their structural integrity.
Di(2-ethylhexyl) Maleate finds primary application in the plastics industry as a secondary plasticizer, particularly in polyvinyl chloride (PVC) formulations, where it contributes flexibility and improved thermal stability.

Di(2-ethylhexyl) Maleate is also used in adhesives, sealants, and coatings due to its compatibility with various resin systems.
Di(2-ethylhexyl) Maleate does not occur naturally in significant quantities and is exclusively produced through industrial synthesis.
The large-scale production process typically involves continuous esterification reactors operating at elevated temperatures with efficient agitation and controlled molar ratios of reactants.

EXTRACTION AND PRESENTATION of DI(2-ETHYLHEXYL) MALEATE:
Di(2-ethylhexyl) Maleate can be produced by catalytic esterification of maleic acid and 2-ethylhexyl alcohol .

CHARACTERISTICS of DI(2-ETHYLHEXYL) MALEATE:
Di(2-ethylhexyl) Maleate is a flammable, difficult to ignite, colorless liquid that is practically insoluble in water.

BENEFITS / KEY CHARACTERISTICS of DI(2-ETHYLHEXYL) MALEATE:
*High molecular weight with very low volatility and thermal stability.
*Excellent compatibility and flexibility-enhancement in polymer systems.
*Transparent and color-stable, with low acid value and moisture content in high-grade grades.
*Hydrophobic character supports durability in coatings and elastomers.

PHYSICAL and CHEMICAL PROPERTIES of DI(2-ETHYLHEXYL) MALEATE:
IUPAC Name: Bis(2‑ethylhexyl) (2 Z)‑but‑2‑enedioate
CAS Number: 142‑16‑5
EC / EINECS Number: 205‑524‑5
PubChem CID: 5365125
ChemSpider ID: 4517207
Appearance: Colorless to pale yellow clear oily liquid
Odor: Mild ester odor, described as slight or faint
Density: ~0.94 g/cm³ at 20 °C
Melting / Pour Point: Around −60 °C
Boiling Point: ~156 °C at ~0.7–1 mmHg (~173 °C at 3 mmHg),
estimated ~410 °C at atmospheric pressure

Flash Point: ~180–185 °C (closed cup)
Vapor Pressure: Negligible (<0.1 Pa at ambient temp)
Refractive Index: ~1.454–1.46 at 20–23 °C
Water Solubility: Practically insoluble (~0.036 mg/L at 20 °C)
log P: ~6.5–7.7 (highly lipophilic)
Other(deleted CASRN): 48075-77-0
ECHA EINECS - REACH Pre-Reg: 205-571-1
FDA UNII: C2F7JHI12L
Nikkaji Web: J36.805I
Beilstein Number: 1729133
MDL: MFCD00027250
XlogP3-AA: 6.50 (est)

Molecular Weight: 340.50372000
Formula: C20 H36 O4
Formula / Mw: C₂₀H₃₆O₄ / ~340.50 g/mol
CAS / EC Number: 142‑16‑5 / 205‑524‑5
Appearance / Odor: Colorless oily liquid / slight ester odor
Density: ~0.94 g/cm³ @ 20 °C
Melting Point: −60 °C
Boiling Point: 156 °C @ ~0.7 mmHg; ~410 °C at atm
Flash Point: 180–185 °C (closed cup)
Vapor Pressure: Negligible (<0.1 Pa)
Refractive Index: ~1.454–1.46 @ 20–23 °C

Water Solubility: ~0.036 mg/L @ 20 °C
log P: ~6.5–7.7
Major Use: Plasticizer/comonomer in polymers
Benefits: Flexibility, transparency, low volatility
Molecular Weight: 340.5 g/mol
XLogP3-AA: 6.5
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 16
Exact Mass: 340.26135963 Da
Monoisotopic Mass: 340.26135963 Da
Topological Polar Surface Area: 52.6 Å²

Heavy Atom Count: 24
Formal Charge: 0
Complexity: 329
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 2
Defined Bond Stereocenter Count: 1
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes

Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Boiling Point: 409.81 °C. @ 760.00 mm Hg (est)
Flash Point: 375.00 °F. TCC (190.40 °C.) (est)
logP (o/w): 7.691 (est)
Soluble in: alcohol
Soluble in: water, 0.001167 mg/L @ 25 °C (est)
Insoluble in: water
Molecular Formula / Molecular Weight: C20H36O4 = 340.50
Physical State (20 deg.C): Liquid

Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN: 142-16-5
Reaxys Registry Number: 1729133
PubChem Substance ID: 87572131
SDBS (AIST Spectral DB): 7571
MDL Number: MFCD00027250
Chemical formula: C20H36O4
Molar mass: 340.504 g·mol−1
Appearance: Colorless liquid
Density: 0.94 g/cm3

Melting point: −60 °C (−76 °F; 213 K)
Boiling point: 156 °C (313 °F; 429 K)
Solubility in water: 0.036 mg/L (20 °C)
Linear Formula: CH3(CH2)3CH(C2H5)CH2O2CCH=CHCO2CH2CH(C2H5)(CH2)3CH3
CAS Number: 142-16-5
Molecular Weight: 340.50
EC Number: 205-524-5
MDL number: MFCD00027250
UNSPSC Code: 12162002
PubChem Substance ID: 24871210
NACRES: NA.23
CBNumber: CB6393335

Molecular Formula: C20H36O4
Molecular Weight: 340.5
MDL Number: MFCD00027250
MOL File: 142-16-5.mol
Melting point: -50°C
Boiling point: 208-209°C 10mm
Density: 0.944 g/mL at 25 °C(lit.)
Pour Point: -50
vapor pressure: 0Pa at 20℃
refractive index: n20/D 1.455(lit.)

Flash point: >230 °F
storage temp.: Sealed in dry, Room Temperature
solubility: Chloroform (Sparingly), Ethyl Acetate(Slightly), Methanol (Slightly)
form: Liquid
color: Colourless
Viscosity: 16cp (25C)
Water Solubility: 18μg/L at 20℃
InChIKey: ROPXFXOUUANXRR-YPKPFQOOSA-N
LogP: 7.24 at 25℃
CAS DataBase Reference: 142-16-5(CAS DataBase Reference)
Indirect Additives used in Food Contact Substances: DI(2-ETHYLHEXYL) MALEATE
FDA 21 CFR: 175.105; 176.180

EWG's Food Scores: 4-7
FDA UNII: C2F7JHI12L
NIST Chemistry Reference: 2-Butenedioic acid (z), di-2-ethylhexyl ester(142-16-5)
EPA Substance Registry System: 2-Butenedioic acid (2Z)-, 1,4-bis(2-ethylhexyl) ester (142-16-5)
UNSPSC Code: 41116107
NACRES: NA.24
Molecular form: C20H36O4
Appearance: Clear Colorless Oil
Mol. Weight: 340.5

Storage: 2-8°C Refrigerator
Molecular Formula: C20H36O4
Molecular Weight: 340.5
InChI: InChI=1S/C20H36O4/c1-5-9-11-17(7-3)15-23-19(21)13-14-20(22)24-16-18(8-4)12-10-6-2/h13-14,17-18H,5-12,15-16H2,1-4H3/b14-13-
InChIKey: ROPXFXOUUANXRR-YPKPFQOOSA-N
Smiles: C(OCC(CC)CCCC)(=O)/C=CC(OCC(CC)CCCC)=O
CAS No: [142-16-5]
Synonyms: Di(2-ethylhexyl) Maleate
Synonyms: Dioctyl Maleate
Product Code: FB62553
MDL No: MFCD00027250
Chemical Formula: C20H36O4

Molecular Weight: 340.5 g/mol
Smiles: CCCCC(CC)COC(=O)/C=CC(=O)OCC(CC)CCCC
Melting Point: -60 °C
Density: 0.944 g/cm3
Flash Point: 185 °C
CAS: 142-16-5
Molecular Formula: C20H36O4
Molecular Weight (g/mol): 340.504
MDL Number: MFCD00027250

InChI Key: ROPXFXOUUANXRR-YPKPFQOOSA-N
PubChem CID: 5365125
IUPAC Name: bis(2-ethylhexyl) (Z)-but-2-enedioate
SMILES: CCCCC(CC)COC(=O)C=CC(=O)OCC(CC)CCCC
Melting Point: -60°C
Color: Colorless
Boiling Point: 173°C
Formula Weight: 340.50

Percent Purity: ≥93.0% (GC)
Physical Form: Liquid
Chemical Name or Material: Bis(2-ethylhexyl) Maleate
InChI: InChI=1S/C20H36O4/c1-5-9-11-17(7-3)15-23-19(21)13-14-20(22)24-16-18(8-4)12-10-6-2/h13-14,17-18H,5-12,15-16H2,1-4H3/b14-13-
InChI Key: ROPXFXOUUANXRR-YPKPFQOOSA-N
Formula: C20H36O4
SMILES: CCCCC(CC)COC(=O)C=CC(=O)OCC(CC)CCCC
Molecular Weight1: 340.50
CAS: 142-16-5

FIRST AID MEASURES of DI(2-ETHYLHEXYL) MALEATE:
-Description of first-aid measures
*General advice:
Show this material safety data sheet to the doctor in attendance.
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with
water/ shower.
*In case of eye contact:
After eye contact:
Rinse out with plenty of water.
Call in ophthalmologist.
Remove contact lenses.
*If swallowed:
After swallowing:
Immediately make victim drink water (two glasses at most).
Consult a physician.
-Indication of any immediate medical attention and special treatment needed.
No data available

ACCIDENTAL RELEASE MEASURES of DI(2-ETHYLHEXYL) MALEATE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Observe possible material restrictions.
Take up dry.
Dispose of properly.
Clean up affected area.

FIRE FIGHTING MEASURES of DI(2-ETHYLHEXYL) MALEATE:
-Extinguishing media:
*Suitable extinguishing media:
Carbon dioxide (CO2)
Foam
Dry powder
*Unsuitable extinguishing media:
For this substance/mixture no limitations of extinguishing agents are given.
-Further information:
Prevent fire extinguishing water from contaminating surface water or the ground water system.

EXPOSURE CONTROLS/PERSONAL PROTECTION of DI(2-ETHYLHEXYL) MALEATE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
Safety glasses
*Body Protection:
protective clothing
*Respiratory protection:
Recommended Filter type: Filter A
-Control of environmental exposure:
Do not let product enter drains.

HANDLING and STORAGE of DI(2-ETHYLHEXYL) MALEATE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Tightly closed.
Dry.

STABILITY and REACTIVITY of DI(2-ETHYLHEXYL) MALEATE:
-Chemical stability:
The product is chemically stable under standard ambient conditions (room temperature).
-Possibility of hazardous reactions:
No data available