- Chlorodiphenylphosphine
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- $0.00 / 200KG
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2024-11-01
- CAS:1079-66-9
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1000mt/year
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| Chlorodiphenylphosphine Basic information |
| Chlorodiphenylphosphine Chemical Properties |
Melting point | 14-16°C | Boiling point | 320 °C(lit.) | density | 1.229 g/mL at 25 °C(lit.) | vapor density | 7.8 (vs air) | vapor pressure | 1.3 hPa (20 °C) | refractive index | n20/D 1.636(lit.) | Fp | >230 °F | storage temp. | Store below +30°C. | solubility | Miscible with alcohol. Slightly miscible with ammonia. | form | Liquid | color | Colorless to yellow | Specific Gravity | 1.229 | Water Solubility | Reacts violently | Sensitive | Air & Moisture Sensitive | Hydrolytic Sensitivity | 8: reacts rapidly with moisture, water, protic solvents | BRN | 512032 | InChIKey | XGRJZXREYAXTGV-UHFFFAOYSA-N | LogP | 5.330 (est) | CAS DataBase Reference | 1079-66-9(CAS DataBase Reference) | NIST Chemistry Reference | Chlorodiphenylphosphine(1079-66-9) | EPA Substance Registry System | Phosphinous chloride, diphenyl- (1079-66-9) |
Hazard Codes | C | Risk Statements | 14-34-29-36 | Safety Statements | 26-36/37/39-45-8-30-25-27 | RIDADR | UN 3265 8/PG 2 | WGK Germany | 2 | F | 1-9-19 | Autoignition Temperature | 320 °C | TSCA | Yes | HazardClass | 8 | PackingGroup | II | HS Code | 29310095 | Toxicity | LD50 orally in Rabbit: 316 mg/kg |
| Chlorodiphenylphosphine Usage And Synthesis |
Chemical Properties | Colorless to light yellow liqui | Uses | Chlorodiphenylphosphine is used to introduce the diphenylphosphinyl moiety by aryl ortho-lithiation. It is also used as an intermediate to make antioxidants, flame retardants, stabilizers, catalysts, photoinitiators, and optical brighteners. Used as a halogenation reagent for the conversion of alcohols into halides, in the preparation of solid-phase reagent for the conversion of alcohols to alkyl halides. | Production Methods |
The specific synthesis steps of Chlorodiphenylphosphine are as follows: In a sealed NMR tube filled with argon,Dissolve Ph2P (O) H (0.05 mmol) in 0.5 mL of tetrahydrofuran,Add acetyl chloride (the amount of acetyl chloride added is 1.2 times the equivalent of Ph2P (O) H),The mixture was reacted at 100 ° C for 12 hours with a yield of 99%.
| Synthesis Reference(s) | Journal of the American Chemical Society, 77, p. 3526, 1955 DOI: 10.1021/ja01618a030 | Flammability and Explosibility | Non flammable | Purification Methods | This air-sensitive, pale yellow lachrymatory liquid is purified by careful fractional distillation and discarding the lower boiling fraction which contains the main impurity PhPCl2 (b 48-51o/0.7mm), and checking for impurities by NMR. [Weinberg J Org Chem 40 3586 1975, Honer et al. Chem Ber 94 2122 1961, Beilstein 16 IV 969.] |
| Chlorodiphenylphosphine Preparation Products And Raw materials |
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