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Safety Information

246808

Sigma-Aldrich

Trimethylolpropane triacrylate

contains monomethyl ether hydroquinone as inhibitor, technical grade

Synonym(s):

TMPTA

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About This Item

Linear Formula:
(H2C=CHCO2CH2)3CC2H5
CAS Number:
Molecular Weight:
296.32
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

grade

technical grade

Quality Level

vapor density

>1 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)

contains

monomethyl ether hydroquinone as inhibitor

refractive index

n20/D 1.474 (lit.)

density

1.1 g/mL at 25 °C (lit.)

SMILES string

CCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C

InChI

1S/C15H20O6/c1-5-12(16)19-9-15(8-4,10-20-13(17)6-2)11-21-14(18)7-3/h5-7H,1-3,8-11H2,4H3

InChI key

DAKWPKUUDNSNPN-UHFFFAOYSA-N

General description

Trimethylolpropanetriacrylate (TMPTA) is a tri-functional monomer that is used in the productionof various types of polymers with a wide range of applications. The most commonuse of trimethylolpropane triacrylate is in the production of UV-curedcoatings, inks, and adhesives, resins, photosensitive materials, andsuperabsorbent materials. Additionally, TMPTA-based polymers are utilized in theproduction of thermosetting resins, which are used in the production ofcomposites, laminates, and coatings. TMPTA can also be copolymerized with othermonomers to tailor the properties of the resulting polymers to meet specificrequirements.

Application

Trimethylolpropane triacrylate can be used as a starting material in the preparation of:
  • Poly(trimethylolpropane triacrylate/Al(PTMPTA/Al) nanocomposites by in situ solution polymerization.
  • Cross-linkable acrylamide/crotonic acid water retainer hydrogels.
  • Polymer electrolyte for dye-sensitized solar cells.

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

382.1 °F - closed cup

Flash Point(C)

194.5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

246808-100G:
246808-500G:
246808-VAR:
246808-5G:
246808-BULK:


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Keng-Chi Cho et al.
Optics express, 19(12), 11732-11739 (2011-07-01)
In this study, the intensity of two-photon excited fluorescence (TPEF) of xanthene dye, Rose Bengal (RB), was significantly enhanced via bovine serum albumin (BSA) microstructures fabricated by the two-photon crosslinking (TPC) technique. The RB was utilized as the photoactivator in
G Gunadi et al.
Dental materials : official publication of the Academy of Dental Materials, 13(1), 7-12 (1997-01-01)
The purpose of this study was to prepare a light-cured adhesive applicable for orthodontics by mixing monomers and a polymerized reactive organic composite filler (prepolymerized trimethylolpropane trimethacrylate-filler, TMPT-filler). The monomer component was a mixture of 3.0 wt% 2-hydroxy-3-(2-naphthoxy)propyl methacrylate (HNPM)
Surface-tension-induced synthesis of complex particles using confined polymeric fluids.
Chang-Hyung Choi et al.
Angewandte Chemie (International ed. in English), 49(42), 7748-7752 (2010-09-04)
Shin-Hyun Kim et al.
Journal of the American Chemical Society, 130(18), 6040-6046 (2008-04-09)
Double emulsion droplets encapsulating crystalline colloidal arrays (CCAs) with a narrow size distribution were produced using an optofluidic device. The shell phase of the double emulsion was a photocurable resin that was photopolymerized downstream of the fluidic channel within 1
Paul Delrot et al.
Optics express, 26(2), 1766-1778 (2018-02-07)
Two-photon polymerization (TPP) processes have enabled the fabrication of advanced and functional microstructures. However, most TPP platforms are bulky and require the use of expensive femtosecond lasers. Here, we propose an inexpensive and compact alternative to TPP by adapting an

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