Grundinformationen
- Standard-SMILES
CCCCCCCCP(CCCCCCCC)CCCCCCCC- InChIKey
RMZAYIKUYWXQPB-UHFFFAOYSA-N- Summenformel
- C24.H51.P
- Durchschnittliche Molmasse
- 370,6 g/mol
- Monoisotopische Masse
- 370,37283826
Namen und Bezeichner
- Bevorzugter Name
- Trioctylphosphine
- IUPAC
- trioctylphosphane
- Lokaler Name
- Trioctylphosphin
- Englischer Name
- Trioctylphosphine
- Summenformel
- C24H51P
- Molmasse
- 370.64
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
4731-53-7- PubChem CID
- 20851
- DTXSID
DTXSID9063582- UNII
- VE0Y037UCN
- EC Number
- 225-234-2
- Nikkaji
- J151.214E
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 10,2
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 21
- Schwere Atome
- 25
- Formalladung
- 0
- Komplexität
- 188
Experimentelle und physikochemische Eigenschaften
Physical Description
Liquid
Colorless liquid with an odor like garlic; [Alfa Aesar MSDS]
Physikochemische Eigenschaften
- Schmelzpunkt
- 30 °C · 30°C
- Siedepunkt
- 284 · 284-291 °C50 mm Hg(lit.)
- Dichte
- 0.831 g/mL · 0.831 g/mL at 25 °C(lit.)
- Brechungsindex
- 20 · n20/D 1.468(lit.)
- Flammpunkt
- 297 °F · 297 °F
- storage temp.
- 2 · 2-8°C, protect from light, stored under nitrogen
- Aggregatzustand
- Powder or Crystalline Powder
- Farbe
- White to off-white
- Wichte
- 0.831 · 0.831
- Wasserlöslichkeit
- Immiscible with water.
- BRN
- 1776995 · 1776995
- InChI
- InChI=1S/C24H51P/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3
- InChIKey
- RMZAYIKUYWXQPB-UHFFFAOYSA-N
- SMILES
- P(CCCCCCCC)(CCCCCCCC)CCCCCCCC
- CAS Datenbank
- 4731 · 4731-53-7(CAS DataBase Reference)
- EPA chemische Informationen
- Phosphine, trioctyl- (4731-53-7)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H314 (75.9%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]
P260, P261, P264, P264+P265, P271, P280, P301+P330+P331, P302+P352, P302+P361+P354, P304+P340, P305+P351+P338, P305+P354+P338, P316, P319, P321, P332+P317, P337+P317, P362+P364, P363, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 87 reports by companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Regulatory Information
Phosphine, trioctyl- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Phosphine, trioctyl- 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)
Status: Active Update: 09-08-2021 https://echa.europa.eu/registration-dossier/-/registered-dossier/19595
Sicherheit und Schutzausrüstung
Protective Action Criteria (PAC)
0.11 [mg/m3]
1.2 [mg/m3]
7.2 [mg/m3]
Toxikologische Informationen
Sicherheitsdaten
- F
- 10-13-23
- wgk
- 2
- tsca
- TSCA listed
- ridadr
- UN 1760 8/PG 2
- hs_code
- 29310099
- RTECS-Nr.
- SZ3450000
- risk_code
- 34-36/37/38
- hazard_code
- C,Xi
- safety_code
- 26-36/37/39-45-37/39
- hazard_class
- 8
- packing_group
- II
- Speicherklasse
- 8A - Combustible corrosive hazardous materials
- Hazard Classifications
- Eye Dam. 1Skin Corr. 1B
Chemie und Industrie
Verwendung und Herstellung
General Manufacturing Information
Computer and Electronic Product Manufacturing
Phosphine, trioctyl-: ACTIVE
Anwendungen
BeschreibungTrioctylphosphine (also known as Tri-n-octylphosphine, abbreviated as TOP) is a weakly basic organophosphorus compound that can be used in the synthesis of nanomaterials (such as metallic nanoparticles). It also serves as the most popular organophosphorus source in oil-phase synthesis, a stabiliser for certain nanorods, and acts as a solvent in certain chemical processes.
VerwendenTri-n-octylphosphine is used for coating zinc sulfide shells on cadmium-selenium quantum dot core by successive ionic layer adsorption and reaction method. It acts as a precursor to trioctylphosphine oxide. Further, it is used as a solvent for cadmium and selenium precursors. It also serves as a common reagent in the chemical synthesis of nanoparticles. It acts as a precursor to trioctylphosphine oxide.
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