Ethylmercury(1+);chloride

Base Information

• Chemical Name: Ethylmercury(1+);chloride
• CAS No.: 107-27-7
• Molecular Formula: C2H5 Cl Hg
• Molecular Weight: 265.105
• Hs Code.: 28521000
• UNII: M04218TP6P
• Mol file: 107-27-7.mol

Synonyms:Ethylmercury(1+);chloride;ETHYLMERCURIC CHLORIDE [MI]

Chemical Property of Ethylmercury(1+);chloride

Chemical Property:

• Appearance/Colour: silver crystals or white solid
• Melting Point: 195°C
• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 0.00000
• Density: g/cm³
• LogP: 1.66090
• Water Solubility.: Insoluble in water. Slightly soluble in ether. Soluble in hot alcohol. Sublimes readilyInsoluble in water. Slightly soluble in e
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 265.978621
• Heavy Atom Count: 4
• Complexity: 2.8

Purity/Quality:

99% ^*data from raw suppliers

EthylmercuryChloride(TechnicalGrade) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T+N
• Hazard Codes: T+,N
• Statements: 26/27/28-33-50/53
• Safety Statements: 13-28-36-45-61-60

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC[Hg+].[Cl-]
• Uses: Ethyl mercuric chloride is used as the polymerization catalyst; seed or bulb fungicide. Applied at 2% strength (soln or mixed with solids) as a fungicide for treating seeds.

Technology Process of Ethylmercury(1+);chloride

There total 46 articles about Ethylmercury(1+);chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%

tetraethyllead(IV) (78-00-2) → diethyllead dichloride (13231-90-8) + ethylmercury(II) chloride (107-27-7)

Guidance literature:

With mercury dichloride; In ethanol; 4h heated at 65°C;; precipitation at cooling;;

Reference yield: 30.0%

tetrachloromethane (56-23-5) + diethylmercury (627-44-1) → mercury(I) chloride (104923-33-3) + ethene (74-85-1) + chloroethane (75-00-3) + ethylmercury(II) chloride (107-27-7) + mercury

Guidance literature:

In neat (no solvent); 150°C, 30 h; further products;

Reference yield: 11.0%

tetrachloromethane (56-23-5) + oxygen (80937-33-3) + diethylmercury (627-44-1) → mercury(I) chloride (104923-33-3) + chloroethane (75-00-3) + chloroform (67-66-3,8013-54-5) + ethylmercury(II) chloride (107-27-7) + mercury

Guidance literature:

In neat (no solvent); 150°C, 50 h; further products;

upstream raw materials:

(Dichloroiodo)benzene

diethylmercury

tetraethyltin

ethylmagnesium chloride

Downstream raw materials:

ethyl-dichloro-(4-methoxy-phenyl)-λ⁴-tellane

diethylmercury

2-Ethylpyridine

4-Ethylpyridine

Refernces

• 1、 Mueller et al.. "". . p. 125,132. Retrieved 1967.
• 2、 Nesmeyanov,Reutov. "". . p. 2803,2805, 2806. Retrieved 1964.
• 3、 Kruglaya et al.. "". . . Retrieved 1977.
• 4、 Nies, J. Dirk,Bellama, Jon M.,Ben-Zvi, Nava. "DIRECT TRANSFER OF ALIPHATIC AND AROMATIC SUBSTITUENTS FROM ORGANOSILATRANES TO MERCURY(II) SPECIES". . p. 315 - 320. Retrieved 2007/10/02.
• 5、 Razuvaev, G. A.,Zhil'tsov, S. F.,Shabanov, A. V.,Lavrent'ev, A. A.. "INFLUENCE OF OXYGEN ON THE REACTIONS OF ORGANOMERCURY COMPOUNDS WITH POLYCHLOROMETHANES". . p. 454 - 462. Retrieved 2007/10/02.