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676-83-5

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676-83-5 Usage

Chemical Properties

Colorless to light yellow liqui

Uses

Methyldichlorophosphine is used to prepare difunctional phosphonoamidite coupling reagents in nucleoside chemistry and "phospha-Wittig"reagents.

General Description

A colorless liquid with a pungent odor. Very toxic by inhalation. Denser than water.

Air & Water Reactions

Highly flammable. Forms fumes containing HCl in moist air. Can spontaneously ignite on contact with moist air. Reacts with water to form hydrochloric acid, reaction may be violent and ignite unreacted material.

Reactivity Profile

METHYLDICHLOROPHOSPHINE is water reactive. Incompatible with strong oxidizing agents, alcohols, bases (including amines). May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Health Hazard

Fire will produce irritating, corrosive and/or toxic gases. Inhalation of decomposition products may cause severe injury or death. Contact with substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution.

Fire Hazard

Flammable/combustible material. May ignite on contact with moist air or moisture. May burn rapidly with flare-burning effect. Some react vigorously or explosively on contact with water. Some may decompose explosively when heated or involved in a fire. May re-ignite after fire is extinguished. Runoff may create fire or explosion hazard. Containers may explode when heated.

Safety Profile

A poison. A corrosive irritant to the skin, eyes, and mucous membranes. Flammable when exposed to heat or flame; can react vigorously with oxidtzing materials. When heated to decomposition it emits very toxic fumes of Cland POx.

Check Digit Verification of cas no

The CAS Registry Mumber 676-83-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,7 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 676-83:
(5*6)+(4*7)+(3*6)+(2*8)+(1*3)=95
95 % 10 = 5
So 676-83-5 is a valid CAS Registry Number.
InChI:InChI=1/CH3Cl2P/c1-4(2)3/h1H3

676-83-5 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (30211)  Methyldichlorophosphine, 97+%   

  • 676-83-5

  • 1g

  • 219.0CNY

  • Detail
  • Alfa Aesar

  • (30211)  Methyldichlorophosphine, 97+%   

  • 676-83-5

  • 5g

  • 1094.0CNY

  • Detail

676-83-5SDS

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 Methyldichlorophosphine

1.2 Other means of identification

Product number -
Other names dichloro(methyl)phosphane

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:676-83-5 SDS

676-83-5Relevant articles and documents

Methylation of Some Cyclic Triphosphenium Ions

Dillon, Keith B.,Olivey, Richard J.

, p. 150 - 154 (2004)

Six cyclic triphosphenium ions, including examples of five-, six-, and seven-membered ring systems, have been successfully methylated by excess methyl triflate to form the corresponding di-cations. This has been unequivocally established by means of

Ulmer et al.

, p. 82 (1961)

Mass spectral study of the CWC-related S-alkyl methylphosphonochloridothioites/S,S′-dialkyl (alkyl′)methylphosphonodithioites under gas chromatography-mass spectrometry conditions

Saeidian, Hamid,Mirkhani, Valiollah,Faraz, Sajjad Mousavi,Sarabadani, Mansour,Naseri, Mohammad Taghi,Ashrafi, Davood,Mirjafary, Zohreh,Babri, Mehran

, p. 13 - 21 (2016)

A class of S-alkyl methylphosphonochloridothioites 3 (11 compounds), S,S′-dialkyl methylphosphonodithioites 4 (12 compounds) and S-alkyl S′-alkyl′ methylphosphonodithioites 5 (9 compounds) were synthesized and were analyzed using gas chromatography-electron ionization mass spectrometer (GC-EIMS). Generalized fragmentation pathways under experimental condition for synthesized compounds are proposed based on analysis of fragment ions of deuterated analogs and density functional theory (DFT) calculations. Results of the study were undertaken with a view to enrich the Organization for the Prohibition of Chemical Weapons (OPCW) Central Analytical Database (OCAD), which may be used for detection and identification of Chemical Weapons Convention (CWC)-related chemicals during on-site inspection and/or off-site analysis, such as OPCW proficiency tests.

Method for synthesizing methyl phosphorus dichloride based on carbon microsphere loaded iron-nickel-cerium catalyst

-

Paragraph 0014; 0016-0018; 0020-0022; 0024-0027, (2021/10/16)

The invention discloses a method for synthesizing methyl phosphorus dichloride based on a carbon microsphere loaded iron-nickel-cerium catalyst. The method comprises the following steps: preparing impregnation liquid, preparing the carbon microsphere loaded iron-nickel-cerium catalyst and synthesizing the methyl phosphorus dichloride. According to the synthesis method, a carbon microsphere loaded iron-nickel-cerium catalyst is adopted, the loading amount of three elements of iron, nickel and cerium accounts for 0.2-1% of the total mass of a carbon microsphere carrier, and the molar ratio of iron-nickel-cerium atoms loaded into carbon microspheres is (49-62): (29-48): (3-9). According to the method, the reaction temperature is low, the temperature is 300-400 DEG C, the conversion rate of phosphorus trichloride is 20.4-30.1%, the yield of methyl phosphorus dichloride is 94.6-97.5%, the catalyst is solid, non-toxic and easy to separate from a reaction system, the service life is 2800-3400 hours, and 3.6-6.5 kg of methyl phosphorus dichloride can be produced by per gram of the carbon microsphere loaded iron-nickel-cerium catalyst.

Method for preparing dichloro monoalkyl phosphine

-

Paragraph 0060-0062, (2017/08/29)

The invention discloses a method for preparing dichloro monoalkyl phosphine. When sodium chloride is used for decomplexing reaction of a binary complex of dichloro monoalkyl aluminum or alkyl aluminum sesquichloride and phosphorus trichloride, alkane solvents are added, the dissociated dichloro monoalkyl phosphine enters the alkane solvents, alkane solution of the dichloro monoalkyl phosphine and newly-generated NaAlCl4 solids are filtered and separated, mixture of the product dichloro monoalkyl phosphine and the alkane solvents can be distilled and separated and can also directly enter a next application process without separation, decomposition of traditional dichloro monoalkyl phosphine in high-temperature distillation is avoided, yield is improved, and waste residues are reduced.

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