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627-49-6

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627-49-6 Usage

General Description

Diethylphosphine, also known as DEP, is a chemical compound with the formula (C2H5)2PH. It is a colorless, highly flammable liquid with a strong, disagreeable odor. Diethylphosphine is primarily used as a reagent in organic synthesis and as a ligand in coordination chemistry. It is also used in the production of pesticides, flame retardants, and other organic phosphorus compounds. Diethylphosphine is highly toxic and can cause irritation to the eyes, skin, and respiratory system upon exposure. It should be handled with extreme caution and appropriate protective measures should be taken when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 627-49-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 627-49:
(5*6)+(4*2)+(3*7)+(2*4)+(1*9)=76
76 % 10 = 6
So 627-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11P/c1-3-5-4-2/h5H,3-4H2,1-2H3

627-49-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylphosphane

1.2 Other means of identification

Product number -
Other names Phosphine, diethyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:627-49-6 SDS

627-49-6Relevant articles and documents

OBERFLAECHEN-REAKTIONEN 15 Heterogene Dechlorierungen von Phosphorchloriden (X)PCl3 und R-PCl2 an , , x/TiO2> und sowie spektroskopische Evidenz fuer das Entstehen von Diphospha-dicyan PC-CP aus Cl2P-CC-PCl2

Bock, H.,Bankmann, M.

, p. 167 - 191 (2007/10/02)

Stimulated by the successful generation of unsaturated molecules with low-coordinated phosphorus centers by heterogeneous surface dechlorination, Cl2P-CC-PCl2 is synthesized and characterized by PE and mass spectra.In addition, curls, wool and catalysts x/TiO2> or are tested as potential dechlorinating agents for phosphorus halides like OPCl3, SPCl3, H3C-PCl2, H5C2-PCl2, (H3C)3C-PCl2 or H5C6-PCl2 in a gasflow reactor under reduced pressure and yield, inter alia, the following representative results: due to the thermodynamically favored formation of , or at the Mg surface, P4 is the only gaseous product identified from reactions of OPCl3 and SPCl3 with metal at higher temperatures.On the contrary, passing H3C-PCl2 at 600K over yields a reaction mixture containing P(CH3)3, (H3C)2P-P(CH3)2 (H3C-P)5 and CH4, which suggests an intermediate formation of surface phosphinidenes Mg>.Analogously, the pentamer (H3C-H2C-P)5 can be isolated from ethyldichlorophosphane.Reaction of the evaporated diphospha-cyanogen precursor Cl2P-C-PCl2 with the catalyst produces predominantly PCl3, and P4, but PE and mass spectra provide evidence that also minor amounts of the hitherto unknown molecule PC-CP are formed.

Evidence for Surface Phosphinidene Intermediates Mg> in the Heterogeneous Dechlorination of Alkyldichlorophosphanes RPCl2 by Mg Metal

Bock, Hans,Bankmann, Martin

, p. 1130 - 1132 (2007/10/02)

The heterogeneous dechlorination of alkyldichlorophosphanes by Mg metal at 600 K yields chemisorbed products which include penta-alkylcyclopentaphosphanes (RP)5, in addition to RnPH(3-n), R2P-PR2, P4, RH, and R-R, and thus provides evidence for surface phosphinidene intermediates Mg>.

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