M188

Maleic anhydride

99%

• Synonyme(s) : 2,5-Furandione
• Formule empirique (notation de Hill) : C₄H₂O₃
• CAS Number: 108-31-6
• Poids moléculaire : 98.06
• Beilstein: 106909
• Numéro CE : 203-571-6
• Numéro MDL: MFCD00005518
• Code UNSPSC : 12162002
• ID de substance PubChem : 24896701
• Nomenclature NACRES : NA.23

Propriétés

• Densité de vapeur: 3.4 (vs air)
• Niveau de qualité: 200
• Pression de vapeur: 0.16 mmHg ( 20 °C)
• Essai: 99%
• Température d'inflammation spontanée: 870 °F
• Limite d'explosivité: 7.1 %
• pb: 200 °C (lit.)
• Pf: 51-56 °C (lit.)
• Chaîne SMILES: O=C1OC(=O)C=C1
• InChI: 1S/C4H2O3/c5-3-1-2-4(6)7-3/h1-2H
• Clé InChI: FPYJFEHAWHCUMM-UHFFFAOYSA-N

Description

Description générale

Maleic anhydride (MA) belongs to the class of monomers known as cyclic dicarboxylic anhydrides. It is commonly used in polymerization reactions to produce various types of polymers such as poly(maleic anhydride) (PMA), maleic anhydride-based resins, and maleic anhydride-butadiene copolymers (MABS), etc. These MA-based polymers find applications in various fields including, polymer blends and coatings, epoxy resins, semiconductor devices, secondary batteries, lithium-ion batteries, resin films, glass fiber, coatings, packaging, water treatment, and drug delivery systems. Additionally, MA can be grafted onto other polymers, to enhance their performance and compatibility with other materials. Grafted polymers find applications in the automotive, packaging, and construction industries. Maleic anhydride is also used as an electron-acceptor monomer in the development of various antimicrobial polymers due to their reactive double bonds and reactive anhydride groups.

The structure of maleic acid consists of four carbon molecules along with carboxylate groups on either ends, with a double bond between the central carbon atoms. The anhydride of maleic acid has five atoms in its cyclic molecule, the unsaturated bond undergoes free radical polymerization in the presence of an initiator.

Application

Maleic anhydride can be used as a monomer:

• In the grafting process of high-density polyethylene (HDPE) by the monomer microencapsulation technique, which enables the introduction of enhanced functionality and improved properties to the polymer for functional coatings, membranes, or surface treatments, adhesives, and coatings.
• In the functionalization of polylactic acid (PLA) and acts as a coupling agent in natural fiber biocomposites. The functionalization improves the compatibility and interfacial adhesion between PLA and natural fibers, leading to enhanced mechanical properties and expanded applications of the resulting biocomposite materials.
• Maleic anhydride may be used in the synthesis of unsaturated polyester resins and as a reactant in synthesizing important products such as agricultural chemicals, lubricant additives, and food acidulatents.

Forme physique

briquettes

Informations sur la sécurité

• Pictogrammes: GHS08,GHS05,GHS07
• Mention d'avertissement: Danger
• Mentions de danger: H302,H314,H317,H334,H372
• Conseils de prudence: P260 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
• Classification des risques: Acute Tox. 4 Oral - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1A - STOT RE 1 Inhalation
• Organes cibles: Respiratory system
• Risques supp: EUH071
• Code de la classe de stockage: 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
• Classe de danger pour l'eau (WGK): WGK 1
• Point d'éclair (°F): 217.4 °F - closed cup
• Point d'éclair (°C): 103 °C - closed cup
• Équipement de protection individuelle: Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges