3524-66-1

Basic information

• Product Name: PENTAERYTHRITOL TRIMETHACRYLATE
• Synonyms: 2,2,2-Tris(methacryloyloxymethyl)ethanol;Bismethacrylic acid 2-hydroxymethyl-2-[(methacryloyloxy)methyl]-1,3-propanediyl ester;Dimethacrylic acid 2-(hydroxymethyl)-2-[(methacryloyloxy)methyl]-1,3-propanediyl ester;Penthaerythritol trimethacrylate;Tetramethylolmethane trimethacrylate;[2-(hydroxymethyl)-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate;2-methylacrylic acid [3-hydroxy-2,2-bis(methacryloyloxymethyl)propyl] ester;PENTAERYTHRITOL TRIMETHACRYLATE
• CAS NO: 3524-66-1
• Molecular Formula: C₁₇H₂₄O₇
• Molecular Weight: 340.37
• EINECS: 222-539-2
• Product Categories: monomer
• Mol File: 3524-66-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 463°Cat760mmHg
• Flash Point: 158.8°C
• Appearance: /
• Density: 1.127g/cm³
• PKA: 13.60±0.10(Predicted)
• CAS DataBase Reference: PENTAERYTHRITOL TRIMETHACRYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: PENTAERYTHRITOL TRIMETHACRYLATE(3524-66-1)
• EPA Substance Registry System: PENTAERYTHRITOL TRIMETHACRYLATE(3524-66-1)

Safety Data

• Statements: 36/38-43
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 3524-66-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H24O7/c1-11(2)14(19)22-8-17(7-18,9-23-15(20)12(3)4)10-24-16(21)13(5)6/h18H,1,3,5,7-10H2,2,4,6H3

Upstream product

• 115-77-5 Pentaerythritol 
• 79-41-4 poly(methacrylic acid) 
• 80-62-6 methacrylic acid methyl ester 

Relevant articles and documents

Process for the Preparation of (Meth)Acrylates of Tetra-Or Polyhydric Alcohols

Process for the preparation of acrylic and methacrylic acid esters by transesterification of (meth)acrylic acid esters of the formula I: where R1 is H or CH3 and R2 is an alkyl radical having 1 to 40 carbon atoms, with alkanols which have four or more esterifiable hydroxyl groups, characterized in that 0.01 to 10% by weight, based on the total reaction mixture, of lithium amide catalysts are used as transesterification catalyst.

ADAMANTANE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF

Adamantane derivatives are represented by Formula (1), (6) or (9) : [In Formula (1), R1 is a hydrogen atom or a methyl group; each of R2 and R3 is, identical to or different from each other, a hydrogen atom or a methyl group; each of A1 and A2 is, identical to or different from each other, a -C(=O)-O- group or -O-C(=O)- group, where the right-hand side of these two groups is on the adamantane ring side; each of X1 and X2 is, identical to or different from each other, a straight- or branched-chain alkylene group having 1 to 12 carbon atoms. In Formula (6), each of R4 and R5 is, identical to or different from each other, a hydrogen atom or a methyl group; each of R6 and R7 is, identical to or different from each other, a hydrogen atom or a methyl group; each of A3 and A4 is, identical to or different from each other, a group represented by the following formula:-A-O-C(=O)- (wherein A5 is a straight- or branched-chain alkylene group having 1 to 6 carbon atoms, where the right-hand side of the above formula is on the adamantane ring side); X is a straight- or branched-chain alkylene group having 1 to 12 carbon atoms; and each of m and n is 0 or 1. In Formula (9), R8 is a hydrogen atom or a methyl group; each of R9 and R10 is, identical to or different from each other, a hydrogen atom or a methyl group; R11 is a hydrogen atom, a straight- or branched-chain alkyl group having 1 to 4 carbon atoms, or a group represented by the following Formula (10): (wherein R12 is an acryloyl group, methacryloyl group, 1-adamantylcarbonyl group or 3,5-dimethyladamant-1-ylcarbonyl group; and s is an integer from 1 to 6); and each of p, q and r is an integer from 1 to 6.] These adamantane derivatives are useful as, for example, raw materials for dental materials.