Grundinformationen
- Standard-SMILES
Cc1cc(C)c(C(=O)P(=O)(C(=O)c2c(C)cc(C)cc2C)c2ccccc2)c(C)c1- InChIKey
GUCYFKSBFREPBC-UHFFFAOYSA-N- Summenformel
- C26H27O3P
- Durchschnittliche Molmasse
- 418,5 g/mol
- Monoisotopische Masse
- 418,16978135
Namen und Bezeichner
- Bevorzugter Name
- Bis-trimethylbenzoyl phenylphosphine oxide
- IUPAC
- [phenyl-(2,4,6-trimethylbenzoyl)phosphoryl]-(2,4,6-trimethylphenyl)methanone
- Englischer Name
- Phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide
- Summenformel
- C26H27O3P
- Molmasse
- 418.47
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
162881-26-7- PubChem CID
- 164512
- DTXSID
DTXSID8044597- ChEMBL
CHEMBL3182971- UNII
- JOV61FMS35
- EC Number
- 423-340-5、605-307-9
- Nikkaji
- J1.013.677F
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 6
- Polarare Oberfläche (TPSA)
- 51,2 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 3
- Frei drehbare Bindungen
- 5
- Schwere Atome
- 30
- Formalladung
- 0
- Komplexität
- 610
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 131 · 131-135 °C(lit.)
- Siedepunkt
- 590 · 590.0±60.0 °C(Predicted)
- Dichte
- 1.17 · 1.17±0.1 g/cm3(Predicted)
- Dampfdruck
- 0 Pa · 0Pa at 20℃
- storage temp.
- Sealed in dry,Room Temperature
- Löslichkeit
- acetone, acetonitrile, toluene, and hexanedioldiacrylate: soluble
- Aggregatzustand
- powder
- Farbe
- Pale Yellow to Yellow
- Wasserlöslichkeit
- 100 μg/L · 100μg/L at 20-21℃
- Kosmetik-Inhaltsstoffe Funktionen
- LIGHT STABILIZER
- InChI
- InChI=1S/C26H27O3P/c1-16-12-18(3)23(19(4)13-16)25(27)30(29,22-10-8-7-9-11-22)26(28)24-20(5)14-17(2)15-21(24)6/h7-15H,1-6H3
- InChIKey
- GUCYFKSBFREPBC-UHFFFAOYSA-N
- SMILES
- P(C1C=CC=CC=1)(=O)(C(C1C(=CC(C)=CC=1C)C)=O)C(C1C(=CC(C)=CC=1C)C)=O
- LogP
- 5.77 · 5.77-5.8 at 22℃
- CAS Datenbank
- 162881 · 162881-26-7
- EPA chemische Informationen
- Phosphine oxide, phenylbis(2,4,6-trimethylbenzoyl)- (162881-26-7)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Warning
H317: May cause an allergic skin reaction [Warning Sensitization, Skin]
P261, P272, P273, P280, P302+P352, P321, P333+P317, P362+P364, and P501 (click each P-code to see the statement)
This chemical does not meet GHS hazard criteria for 0.1% (1 of 776) of reports.
Warning
H317 (99.9%): May cause an allergic skin reaction [Warning Sensitization, Skin]
Gefahrenhinweise
Regulatory Information
Chemical: Methanone, 1,1â²-(phenylphosphinylidene)bis[1-(2,4,6-trimethylphenyl)-
Methanone, 1,1'-(phenylphosphinylidene)bis[1-(2,4,6-trimethylphenyl)- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Methanone, 1,1'-(phenylphosphinylidene)bis[1-(2,4,6-trimethylphenyl)- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
PMN - indicates a commenced PMN (Pre-Manufacture Notices) substance.
Status: Active Update: 11-10-2022 https://echa.europa.eu/registration-dossier/-/registered-dossier/11625
Phosphine oxide, phenylbis(2,4,6-trimethylbenzoyl)-: Does not have an individual approval but may be used under an appropriate group standard
Hazard Classes and Categories
Skin Sens. 1 (99.9%)
Skin Sens. 1 (99.8%)
Skin sensitisation - category 1A
Skin sensitization - Category 1A
Skin Sens. 1A
Sicherheitsdaten
- wgk
- -
- tsca
- TSCA listed
- hs_code
- 29319090
- risk_code
- 43-53
- hazard_code
- Xi
- safety_code
- 22-24-37-61
- Speicherklasse
- 11 - Combustible Solids
- Hazard Classifications
- Aquatic Chronic 4Skin Sens. 1
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
Adhesive Manufacturing
Methanone, 1,1'-(phenylphosphinylidene)bis[1-(2,4,6-trimethylphenyl)-: ACTIVE
Anwendungen
VerwendenPhenylbis(2,4,6-trimethylbenzoyl)phosphine oxide is a useful research chemical compound.
Vor- und nachgelagerte Produkte
Vorgelagerte Rohstoffe
Anbieter50 Anbieter
Ergänzende Hinweise
DefinitionPhenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (PPO) has a local absorption maximum in the visible spectrum at 405 nm and could provide sufficient initiating radicals to crosslink polyamic diacrylate ester in NMP[1]. Phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (GR-XBPO) could be used as the reductant, and Monoethanolamine as the oxygen inhibition agent. After UV irradiation, oxygen-containing groups (OCGs) on the graphene oxide (GO) plane and edges are largely removed due to the reduction of GO by free radicals generated by photoinitiator decomposition[2].
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