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ChemicalBook--->CAS DataBase List--->624-48-6

624-48-6

624-48-6 Structure

624-48-6 Structure
IdentificationMore
[Name]

Dimethyl maleate
[CAS]

624-48-6
[Synonyms]

2-BUTENEDIOIC ACID (Z)-,DIMETHYL ESTER
CIS-DIMETHYL BUTENEDIOATE
DIMETHYL MALEATE
DIMETHYL MALEINATE
DMM
MALEIC ACID, BIS-METHYL ESTER
MALEIC ACID DIMETHYL ESTER
METHYL MALEATE
2-Butendioic acid, dimethyl ester,-E-)
2-Butenedioic acid, dimethyl ester, (Z)-
cis-butenedioicacid,dimethylester
Dimethyl (2Z)-2-butenedioate
Dimethyl cis-butenedioate
Dimethyl cis-ethylenedicarboxylate
Dimethylester kyseliny maleinove
dimethylester,(z)-2-butenedioicaci
dimethylesterkyselinymaleinove
Sipomer DMM
Sipomer DMM 6
sipomerdmm
[EINECS(EC#)]

210-848-5
[Molecular Formula]

C6H8O4
[MDL Number]

MFCD00008459
[Molecular Weight]

144.13
[MOL File]

624-48-6.mol
Chemical PropertiesBack Directory
[Appearance]

colourless liquid
[Melting point ]

-19°C
[Boiling point ]

204-205 °C(lit.)
[density ]

1.152 g/mL at 25 °C(lit.)
[vapor pressure ]

48Pa at 25℃
[refractive index ]

n20/D 1.441(lit.)
[Fp ]

196 °F
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

water: soluble77.9g/L at 20°C
[form ]

Liquid
[color ]

Clear
[Odor]

mild char. odor
[Stability:]

Stable. Combustible. Incompatible with acids, bases, reducing agents, strong oxidizing agents.
[Water Solubility ]

Miscible with water.
[BRN ]

471705
[LogP]

0.52 at 35℃
[CAS DataBase Reference]

624-48-6(CAS DataBase Reference)
[NIST Chemistry Reference]

2-Butenedioic acid (Z)-, dimethyl ester(624-48-6)
[EPA Substance Registry System]

624-48-6(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

R21/22:Harmful in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
R43:May cause sensitization by skin contact.
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37:Wear suitable protective clothing and gloves .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
[RIDADR ]

UN 2810 6.1/PG 3
[WGK Germany ]

1
[RTECS ]

EM6300000
[TSCA ]

Yes
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[HS Code ]

29171990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Methanol-->Dimethyl acetylenedicarboxylate
[Preparation Products]

2-Chloro-6-fluorophenylacetic acid-->METHYL 2-CHLORO-6-FLUOROPHENYLACETATE-->DIMETHYL 2-(2-CHLORO-6-NITROPHENYL)MALONATE-->Dimethyl 4-aminothiophene-2,3-dicarboxylate hydrochloride-->2-Phosphonobutane-1,2,4-tricarboxylic acid-->1,2-Benzenedicarboxylic acid, 3,5-dimethyl-, 1,2-dimethyl ester-->(-)-Dimethyl D-tartrate-->Diisobutyl maleate-->2,3-NAPHTHALENEDICARBOXYLIC ACID DIMETHYL ESTER-->DIMETHYL 3-NITROPHTHALATE-->Dimethyl oxalate-->Tetrahydrofuran-->Methyl 2-(4-benzyl-3-oxo-2-piperazinyl)acetate-->dimethyl (dimethoxyphosphinyl)succinate
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Dimethyl maleate(624-48-6).msds
Hazard InformationBack Directory
[Chemical Properties]

colourless liquid
[Uses]

Dimethyl maleate is widely used in the plastics and chemical industries and as a vaporization retardant of insecticides.
[Definition]

ChEBI: A maleate ester resulting from the formal condensation of both carboxy groups of maleic acid with methanol. It is commonly used as a dienophile for Diels-Alder-type cycloaddition reactions in organic synthesis.
[Preparation]

Dimethyl maleate can be synthesized from maleic anhydride and methanol, with sulfuric acid acting as acid catalyst, via a nucleophilic acyl substitution for the monomethyl ester, followed by a Fischer esterification reaction for the dimethyl ester.
[General Description]

Dimethyl maleate (DMM) is a reactive dienophile and undergoes ultrasonic irradiation promoted Diels-Alder reaction with substituted furans. Mesoporous siliceous SBA-15-supported Cu catalyzed gas phase hydrogenolysis of DMM to 1,4-butanediol (BDO) has been reported. Aluminium chloride has been reported to accelerate the Diels-Alder reaction of DMM and anthracene. DMM can be synthesized by the esterification of maleic anhydride with sulfuric acid and methanol.
[Flammability and Explosibility]

Nonflammable
Spectrum DetailBack Directory
[Spectrum Detail]

Dimethyl maleate(624-48-6)MS
Dimethyl maleate(624-48-6)1HNMR
Dimethyl maleate(624-48-6)13CNMR
Dimethyl maleate(624-48-6)IR1
Dimethyl maleate(624-48-6)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Dimethyl maleate, 96%(624-48-6)
[Alfa Aesar]

Dimethyl maleate, 96%(624-48-6)
[Sigma Aldrich]

624-48-6(sigmaaldrich)
[TCI AMERICA]

Dimethyl Maleate,>95.0%(GC)(624-48-6)
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