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Dibenzylammonium dibenzyl dithiocarbamate is a white to light yellow crystalline powder that is soluble in organic solvents such as benzene and toluene. It is a member of the dithiocarbamate class of chemicals and is commonly used as a rubber accelerator in the production of vulcanized rubber. DIBENZYLAMMONIUM DIBENZYLDITHIOCARBAMATE is known for its high efficiency in promoting the cross-linking of rubber molecules, resulting in improved tensile strength and resistance to abrasion and aging.

66216-84-0

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  • Carbamodithioic acid, bis(phenylmethyl)-, compd. with N-(phenylmethyl)benzenemethanamine (1:1)

    Cas No: 66216-84-0

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  • Carbamodithioic acid, bis(phenylmethyl)-, compd. with N-(phenylmethyl)benzenemethanamine (1:1)

    Cas No: 66216-84-0

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66216-84-0 Usage

Uses

Used in Rubber Industry:
Dibenzylammonium dibenzyl dithiocarbamate is used as a rubber accelerator for the production of vulcanized rubber. It accelerates the vulcanization process, which is essential for creating rubber products with improved tensile strength, resistance to abrasion, and aging. Its high efficiency in promoting the cross-linking of rubber molecules makes it a valuable component in the rubber industry.
However, it is important to handle dibenzylammonium dibenzyl dithiocarbamate with caution, as it is considered to be toxic and may cause skin and eye irritation upon contact. Proper safety measures should be taken to minimize exposure and potential health risks associated with this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 66216-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,1 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66216-84:
(7*6)+(6*6)+(5*2)+(4*1)+(3*6)+(2*8)+(1*4)=130
130 % 10 = 0
So 66216-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H15NS2.C14H15N/c17-15(18)16(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14;1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2,(H,17,18);1-10,15H,11-12H2

66216-84-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-1-phenylmethanamine,dibenzylcarbamodithioic acid

1.2 Other means of identification

Product number -
Other names n-benzyl(phenyl)methanaminium dibenzylcarbamodithioate

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:66216-84-0 SDS

66216-84-0Relevant articles and documents

Barium and titanium dithiocarbamates as precursors for colloidal nanocrystals of emerging optoelectronic materials

Creutz, Sidney E.,Donnadieu, Bruno,Ingram, Nicole E.,Jordan, Brian J.

supporting information, p. 15978 - 15982 (2021/11/27)

The synthesis and structures of N,N-dialkyldithiocarbamate complexes of barium are reported; the compounds crystallize as one-dimensional coordination polymers. In combination with a titanium dithiocarbamate precursor, the compounds are demonstrated as competent single-source precursors for the solution-based preparation of colloidal BaTiS3 nanorods. This journal is

Glycosyl dithiocarbamates: β-selective couplings without auxiliary groups

Padungros, Panuwat,Alberch, Laura,Wei, Alexander

, p. 2611 - 2624 (2014/04/17)

In this article, we evaluate glycosyl dithiocarbamates (DTCs) with unprotected C2 hydroxyls as donors in β-linked oligosaccharide synthesis. We report a mild, one-pot conversion of glycals into β-glycosyl DTCs via DMDO oxidation with subsequent ring opening by DTC salts, which can be generated in situ from secondary amines and CS2. Glycosyl DTCs are readily activated with Cu(I) or Cu(II) triflate at low temperatures and are amenable to reiterative synthesis strategies, as demonstrated by the efficient construction of a tri-β-1,6-linked tetrasaccharide. Glycosyl DTC couplings are highly β-selective despite the absence of a preexisting C2 auxiliary group. We provide evidence that the directing effect is mediated by the C2 hydroxyl itself via the putative formation of a cis-fused bicyclic intermediate.

Dibenzylammonium and Sodium Dibenzyldithiocarbamates as Precipitants for Preconcentration of Trace Elements in Water for Analysis by Energy Dispersive X-ray Fluorescence

Moore, Robert V.

, p. 895 - 897 (2007/10/02)

Precipitation with combined dibenzylammonium dibenzyldithiocarbamate and sodium dibenzyldithiocarbamate at pH 5.0 can be used to separate 22 trace elements from water.Membrane filtration of the precipitate yielded a thin sample, suitable for analysis by energy dispersive X-ray fluorescence spectrometry.Alkalis, alkaline earths, lanthanides, and halides were not precipitated, permitting a clean separation of trace elements from the macro constituents of drinking water and drinking water supplies.Methods are given for preparation of reagents of higher purity than previo usly described.

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