General description Sodium diethyldithiocarbamate trihydrate may be used: • To synthesize cis-dichlorobis(N,N-diethyldithiocarbamato) tin(IV) by reacting with tin(II) chloride. • As an alternative to xanthates to generate carbamoyl radical precursors.
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tdec pd (*) tellurium diethyl dithiocarbamate 20 500 orange 20941-65-5 . dbtu cra dibutyl thiourea p 20 500 white 109-46-6 p detu cr diethyl thiourea p 20 500 white 105-55-5 p dptu pd diphenyl thiourea p 20 400 white 102-08-9 p etu c ethylene thiourea p 20 500 white 96-45-7 p
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Tellurium Diethyl Dithiocarbamate; ： ：,,25 ： ：; ： CAS NO：20941-65-5 /： /：C 20 H 40 N 4 S 8 Te ：721 ： .
Tellurium dimethyl-bis(alkylxanthates) of the type R2Te(S2COR')2 with R = CH3 and R' = CH3, C2H 5, i-CsH 7 are obtained by reaction of tellurium dimethyldiiodide with freshly prepared sodium xanthates.
Hazardous Substances Data Bank - Ethyl Tellurac. EPA - Substance Registry Services - Ethyl Tellurac. Local: Primary or secondary rubber accelerator used invery fast curing. SALES SPECIFICATION: APPEARANCE. orange to yellow powder dust suppressed. CONTENT. 96.0 - 99.0%. MELTING POINT. 108 C min. TELLURIUM. 17.0-19.0%. HEAT LOSS. 0.5% max. OIL .
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Typical Product Specifications & Properties Tellurium diethyl dithiocarbamate CAS Number: 20941-65-5 Specifications Limits Molecular weight 720.68 EINECS 244-121-9
Synthesis, Spectroscopic Studies, and Structural Studies of O,O-Alkylene Dithiophosphate and N,N-Dimethyl and Diethyl Dithiocarbamate Derivatives of Halodimethyltellurium(IV). Inorganic Chemistry 1999, 38 (18), 3994-4004. DOI: 10.1021/ic990281f.
Abstract Triphenyltellurium(IV) diethyldithiocarbamate has been synthesized and subjected to single crystal structure determination which indicates that in the solid state the molecule exists as a centrosymmetric dimer in which the diethyl dithiocarbamate ligand can be considered as acting as a bridge (through its two sulfur atoms) with long Te—S bonds.
FUNGICIDAL AND PHYTOCIDAL PROPERTIES OF SOME METAL DIALKYL DITHIOCARBAMATES ' By M. C. GOLDS WORTHY, associate pathologist, E. L. GREEN, associate biochemist, and M, A. SMITH, associate pathologist.Division of Fruit and Vegetable Crops and Diseases, Bureau of Plant Industry, Agricultural Research Administration,
2009 8 – 2017 2 7 7 . "A synthesis method of tellurium diethyl dithiocarbamate" has been granted the national patent (patent number: ZL01105884.6) through our self-reliance and innovation. Green production technology of TETD has been developed and superseded the traditional process with the nitrite as the raw .
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We pay great attentions to increasing the scientific and technological contents in the meantime of promoting innovation and deepening enterprises management. "A synthesis method of tellurium diethyl dithiocarbamate" has been granted the national patent (patent number: ZL01105884.6) through our self-reliance and innovation.
synthesis and characterization of some new heterocyclic tellurium(iv)– dithiocarbamate complexes Article (PDF Available) · January 2005 with 34 Reads How we measure 'reads'
TDEC PD (*) Tellurium diethyl dithiocarbamate 20 500 Orange 20941-65-5 244-121-9 ZBEC C/PD Zinc dibenzyl dithiocarbamate 15 300 White 14726-36-4 238-778-0 . DBTU CRA Dibutyl thiourea 20 500 White 109-46-6 203-647-6 DETU CR Diethyl thiourea 20 500 White 105-55-5 203-308-5
Accelerator MZX (Zinc Dibutyl Dithiocarbamate) Accelerator CuDD (Copper Dibutyl Dithiocarbamate) Accelerator CZ-1 (N, N Dimethyl Cyclohexyl Ammonium Dithiocarbamate) Accelerator TDEC (Tellurium Diethyl Dithiocarbamate) Accelerator ZBED (Zinc Dibenzyl Dithiocarbamate) Accelerator ZDBCX (Zinc Dibutyl Dithiocarbamate Dibutylamine Complex)
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