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Trimethylsulphonium Iodide

TMSOI; RARECHEM AQ A1 0066; Trimethylsulfoxonium; trimethyl-sulfoxoniuiodide; TRIMETHYLSULFOXONIUM IODIDE; trimethylsulphoxoniumioidie; Trimethylsulfoxonium iodate; Trimethysulfoxonium Iodide; TRIMETHYLSULPHOXONIUM IODIDE; trimethylsulfoxoniuim iodide

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Trimethylsulphoxonium Iodide

TMSOI; RARECHEM AQ A1 0066; Trimethylsulfoxonium; trimethyl-sulfoxoniuiodide; TRIMETHYLSULFOXONIUM IODIDE; trimethylsulphoxoniumioidie; Trimethylsulfoxonium iodate; Trimethysulfoxonium Iodide; TRIMETHYLSULPHOXONIUM IODIDE; trimethylsulfoxoniuim iodide

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Trimethyltin Chloride

Trimethyltin chloride is an organotin compound. It is used as a source of the trimethylstanyl group. It is a precursor to compounds used in PVC stabilization.

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Trinitrotoluene

Trinitrotoluene is a chemical compound. It is sometimes used as a reagent in chemical synthesis.

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Triphenylarsine

Triphenylarsine is an organoarsenic compound. It is used as a ligand and a reagent in coordination chemistry and organic synthesis. It is the precursor to tetraphenylarsonium chloride, a popular precipitating agent. It forms complexes with low valent metals that are analogous to the corresponding triphenylphosphine derivatives.

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Triphenylmethyl Chloride

Triphenylmethyl chloride is used as an intermediate in preparation of dyes and pharmaceuticals, It is also used as an antiviral drug .

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Triphenylmethyl Hexafluorophosphate

Triphenylmethyl hexafluorophosphate is an organic salt. It is used as a catalyst and reagent in organic syntheses. It is used in hydride and alkoxy abstractions.

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Triphenylsulfonium Triflate

Triphenylsulfonium triflate is a chemical compound. It consists of a sulfonium cation and the triflate anion. Many related salts are known including those with other noncoordinating anions and those with diverse substituents on the phenyl rings. These compounds are photoacids, releasing strong acids upon photolysis, which is useful in photolithography.

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Triphosgene

Triphosgene is a chemical compound that is used as a safer substitute for phosgene, because at room temperature it is a solid crystal, as opposed to phosgene which is a gas. It is used in organic synthesis to bond one carbonyl group to two alcohols, as in the synthesis of octalactin B. It is prepared by exhaustive chlorination of dimethyl carbonate.

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