Substance
ID:306193
Names and Identifiers
IUPAC name
di-tert-butyl(2,2-dimethylpropyl)phosphane
IUPAC Traditional name
di-tert-butyl(2,2-dimethylpropyl)phosphane
Synonyms
Bis(1,1-dimethylethyl)(2,2-dimethylpropyl)phosphineDi-tert-butylneopentylphosphine二叔丁基新戊基膦
Properties
Product Information
Empirical Formula (Hill Notation)
C13H29P
Purity
95%
Physical Property
Boiling Point
40 °C/0.1 mmHg
Density
0.839 g/mL at 25 °C
Refractive Index
n20/D 1.478
Safety Information
European Hazard Symbols
Corrosive (C)
Flammable (F)Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
Risk Statements
17-21/22-34
GHS Pictograms
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Storage Temperature
-20°C
MSDS Link
Safety Statements
26-36/37/39-45
Packing Group
1
German water hazard class
3
GHS Hazard statements
H250-H302-H312-H314
GHS Signal Word
Danger
GHS Precautionary statements
P222-P231-P280-P305+P351+P338-P310-P422
UN Number
2845
Hazard Class
4.2
RID/ADR
UN 2845 4.2/PG 1
Molecule Details
Packaging
1 g in glass bottle
Application
Reactant for:
• Highly active palladium complexes1
• Synthesis of organometallic compounds of iridium and rhodium2Ligand for cross coupling of aryl bromides and chlorides3
1 g in glass bottle
Application
Reactant for:
• Highly active palladium complexes1
• Synthesis of organometallic compounds of iridium and rhodium2Ligand for cross coupling of aryl bromides and chlorides3
Molecular Spectra
No Data Available
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References
No Data Available
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