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415952

Sigma-Aldrich

Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide

97%

Synonym(s):

(2,4,6-Trimethylbenzoyl)diphenylphosphine oxide, (Diphenylphosphoryl)(mesityl)methanone, 2,4,6-Trimethylbenzoylphenyl phosphinate

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About This Item

Linear Formula:
(CH3)3C6H2COP(O)(C6H5)2
CAS Number:
75980-60-8
Molecular Weight:
348.37
EC Number:
278-355-8
MDL number:
MFCD00192110
UNSPSC Code:
12162002
PubChem Substance ID:
24866046
NACRES:
NA.23

Assay

97%

form

powder

mp

88-92 °C (lit.)

SMILES string

Cc1cc(C)c(c(C)c1)C(=O)P(=O)(c2ccccc2)c3ccccc3

InChI

1S/C22H21O2P/c1-16-14-17(2)21(18(3)15-16)22(23)25(24,19-10-6-4-7-11-19)20-12-8-5-9-13-20/h4-15H,1-3H3

InChI key

VFHVQBAGLAREND-UHFFFAOYSA-N

General description

Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO) is a monoacylphosphine oxide based photoinitiator that can be incorporated in a variety of polymeric matrixes for efficient curing and color stability of the resin.

Application

TPO can be used in the photo-crosslinking of PMMA composite, which can further be used as a gate insulator in organic thin film transistors (OTFTs). It can also be used in the formation of UV curable urethane-acrylate coatings. It may also be used in the photoinduced reaction for the formation of organophosphine compounds, which potentially find their usage as ligands with metal catalysts and reagents.

Storage and Stability

light sensitive

Signal Word

Warning

Hazard Statements

H317,H361f,H411

Hazard Classifications

Aquatic Chronic 2 - Repr. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Coating performance and characteristics for UV-curable aliphatic urethane acrylate coatings containing norrish type I photoinitiators
Lee B, et al.
Journal of Coatings Technology and Research, 3(3), 221-229 (2006)
Amirali Nojoomi et al.
Nature communications, 12(1), 603-603 (2021-01-29)
Two-dimensional (2D) growth-induced 3D shaping enables shape-morphing materials for diverse applications. However, quantitative design of 2D growth for arbitrary 3D shapes remains challenging. Here we show a 2D material programming approach for 3D shaping, which prints hydrogel sheets encoded with
Tomasz Szymborski et al.
Micromachines, 9(4) (2018-11-15)
Organic syntheses based on photochemical reactions play an important role in the medical, pharmaceutical, and polymeric chemistry. For years, photochemistry was performed using high-pressure mercury lamps and immersion-wells. However, due to excellent yield, control of temperature, selectivity, low consumption of
Yong-Chan Jeong et al.
Materials (Basel, Switzerland), 12(7) (2019-04-11)
Despite their excellent electrical and optical properties, Ag nanowires (NWs) suffer from oxidation when exposed to air for several days. In this study, we synthesized a Cs carbonate-incorporated overcoating layer by spin-coating and ultraviolet curing to prevent the thermal oxidation
PMMA-based patternable gate insulators for organic thin-film transistors
Kim TG, et al.
Synthetic Metals, 159(7-8), 749-753 (2009)
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