2-(Methacryloyloxy)ethyl acetoacetate

• Catalog No.: 360767
• CAS Number: 21282-97-3
• M. F.: C10H14O5
• M. W.: 214.21516
• Purity: 95%

SYNONYMS

• Title: 乙酰乙酸甲基丙烯酸乙二醇酯
• IUPAC name: 2-[(2-methylprop-2-enoyl)oxy]ethyl 3-oxobutanoate
• IUPAC Traditional name: 2-[(2-methylprop-2-enoyl)oxy]ethyl 3-oxobutanoate
• Synonyms: Ethylene glycol monoacetoacetate monomethacrylate; 3-氧代丁酸-2-[2-甲基-2-丙烯酰基)氧]乙基酯; 2-甲基丙烯酸乙酰乙酸氧乙酯; Lonzamon AAMEA PQ; (2-Acetoacetoxy)ethyl methacrylate

DATABASE IDS

• MDL Number: MFCD00054405
• Beilstein Number: 2099809
• CAS Number: 21282-97-3
• EC Number: 244-311-1

PROPERTIES

• Contains: 3,000 ppm BHT as inhibitor
• Linear Formula: CH3COCH2CO2CH2CH2O2CC(CH3)=CH2
• Purity: 95%
• Boiling Point: 100 °C/0.8 mmHg(lit.)
• Density: 1.122 g/mL at 25 °C(lit.)
• Flash Point: 113 °C
• Flash Point: 235 °F
• Refractive Index: n20/D 1.456(lit.)
• European Hazard Symbols: Irritant (Xi)
• Risk Statements: 36/37/38-43
• Safety Statements: 26-36
• German water hazard class: 1

DETAILS

Description (English)

Application
Comonomer in coatings and adhesives. Binds to proteins.
Features and Benefits
Acrylic monomer. Forms chelates with metal salts. Functional groups available for condensation reactions and cross-linking. Promotes adhesion to metal surfaces.

Description (简体中文)

Application
用于涂料和粘合剂中的共聚单体。与蛋白质结合。
Features and Benefits
丙烯酸单体。与金属盐形成螯合物。缩合反应和交联可用的官能团。促进与金属表面的粘附。