- Thionyl chloride
or thionyl dichloride is an inorganic compound with the formula SOCl2.
- SOCl2 is a
reactive chemical reagent used in chlorination reactions.
- It is a
colorless, distillable liquid at room temperature and pressure that
decomposes above 140 °C.
- Thionyl chloride
is a colorless to pale yellow liquid used in the production of
batteries.
- N-Acylhydrazones of
o-hydroxyaryl ketones react with thionyl chloride to give
N-arylhydrazonoyl chlorides in good yields.
- Some heteroaromatic
compounds with methyl substituents in the heterocyclic ring, such as
2-methylbenzothiazole, 2-methylbenzoxazole, and analogues, undergo rapid
methyl group chlorination when heated with thionyl chloride.
-
The slow monochlorination, observed in
a few cases, is probably a simple free radical reaction. Thionyl
chloride slowly decomposes at reflux temperature into sulphur monoxide
and chlorine.
-
Lithium thionyl chloride batteries are mainly used in
implantable devices which consume higher power in milliwatt range such
as drug pumps and neurostimulators.
-
When the equilibrium is shifted by the expansion lowering
the pressure in the manifold, more thionyl chloride desorbs from the
carbon increasing the pressure back to the original value.
-
If the thionyl chloride was irreversibly adsorbed or
reacted, the pressure would be expected to decrease and remain at that
lower pressure upon expansion. This discovery lead to a search for a new
getter for Li/SOClz batteries.
-
Alcohols investigated include polyvinyl alcohol, cellulose
and sugars. Alcohols are quite reactive with thionyl chloride.
- Thionyl chloride is
used inside lithium-thionyl chloride batteries as the positive active
material with lithium as the negative active material.
- It is also used as a
reagent for the production of other chemical compounds or
materials.
- It is also used during
synthesis of drugs, vitamins, and herbicides. It is commercially
available and used in industrial chemical reactions.
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General & Process
- About thionyl chloride
- Purification of Thionyl Chloride
- Reactions of N-acylhydrazones with thionyl chloride
- The Reaction of Thionyl Chloride with Methyl-Substituted
Heteroaromatic Compounds
Patent & Technology
- Recovery of thionyl chloride
- Purification of thionyl chloride
- Absorption media for irreversibly gettering thionyl chloride
- Coating for lithium anode, thionyl chloride active cathode
electrochemical cell
- Production of thionyl chloride from hydrogen chloride, sulfur, and
oxygen
- Processes for production of thionyl chloride
- Preparation of thionyl chloride and phosphorus oxyhloride from
sulfur dioxide
- Process for the preparation of thionyl chloride
- An Integrated Battery-Hardware Model for Portable Electronics
- Histochemical Specific Demonstration of the Carboxyl Group in Tissue
Sections
Company Profiles
- Company from Japan
- Company from Mumbai
- Company from Shandong Province
- Company from Zhejiang
Functions
- Synthesis and Characterization of New Diketone Analogues of
Podophyllotoxin
- The synthesis of esters of ursolic acid
- A facile synthesis of
10-methoxy-4,8-dinitro-6H-benzothieno2,3-chromen-6-one
- Synthesis of amino acid methyl ester hydrochloride
- Properties of carbonyl compounds -carboxylic acid derivatives
- Synthesis and Properties of Thiadiazolo pyrimidine Derivatives
Including Their Mesoionic Compounds
- Solid-Phase Stereoselective Synthesis of Disubstituted Ethenes from
Polymer-Sopported α-Selenoaldehydes
- Synthesis of N-chloromethanimidoyl Chloride
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Consultants
- Consultant from Gujarat
- Another consultant from Gujarat
- Consultant from Indiana
- Consultant from Minnesota
- Consultant from New York
Material Safety Data
Sheet
- Thionyl Chloride
- Lithium Thionyl Chloride Battery
- Msds of thionyl chloride
- MSDS of lithium thionyl chloride battery
- Thionyl chloride, 99.5+%
- Safety
data for thionyl chloride
- Lithium /Thionyl chloride single cells and multi-cell battery packs
Products &
Applications
- Thionyl chloride reagent grade, 97%
- Thionyl chloride ReagentPlusŪ, 99.5%, low iron
- Thionyl chloride solution 2.0 M in methylene chloride
- Bioengineering Applications of Lithium Batteries
- How to Choose a Primary Battery
- Particle size reduction and distribution from harnmer-milling
Safety & Hazards
- Chemical data sheet for thionyl chloride
- Thionyl chloride
- Occupational safety and health guideline for thionylchloride
- Nerve Agent Precursor: Thionyl chloride
Pocket guide for thionyl chloride
Thionyl chloride
Report
- Thionyl-Chiorideinduced Lung Injury and Bronchiolitis Obliterans
- Guideline levels for thionyl chloride
- Analysis of a Lithium/Thionyl Chloride Battery under Moderate-Rate
Discharge
- Computational Fluid Dynamics Modeling of a Lithium/Thionyl Chloride
Battery with Electrolyte Flow
- Eastern horizons
- Analytical problem solving in lithium battery
technology
- Advanced Lithium Battery Technology Key to AMR Market
Suppliers
- Suppliers of Thionyl chloride
- Exporters of thionyl chloride
- Thionyl chloride suppliers
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