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S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID, also known as ADTGA, is a thiol-based chemical compound with the molecular formula C6H11NO2S2. It is recognized for its strong chelating and binding properties, which make it a versatile component in the production of metal chelating agents, pharmaceuticals, and as a building block for organic synthesis. Its utility extends to various industrial and scientific applications, including its role as a corrosion inhibitor in industrial processes and as an ingredient in personal care products and cosmetics. Furthermore, ADTGA has potential applications in the treatment of metal poisoning and as a chemoprotective agent in medical research.

4007-01-6

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4007-01-6 Usage

Uses

Used in Chemical Synthesis:
ADTGA is used as a building block in organic synthesis for the creation of various chemical compounds due to its reactive thiol group and strong chelating properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ADTGA is used as a precursor in the development of new drugs, leveraging its chelating capabilities to enhance drug delivery and effectiveness.
Used as a Metal Chelating Agent:
ADTGA is utilized as a metal chelating agent for the removal or stabilization of metal ions in various applications, including environmental remediation and industrial processes.
Used in Corrosion Inhibition:
ADTGA serves as a corrosion inhibitor in industrial processes, protecting metal surfaces from degradation and extending the lifespan of equipment.
Used in Personal Care Products and Cosmetics:
In the personal care and cosmetics industry, ADTGA is used as an ingredient for its chelating properties, which can improve the stability and effectiveness of formulations.
Used in Treatment of Metal Poisoning:
ADTGA has potential applications in the medical field for the treatment of metal poisoning, where its strong binding affinity can aid in the detoxification process.
Used as a Chemoprotective Agent in Medical Research:
In medical research, ADTGA is explored as a chemoprotective agent, potentially protecting healthy cells from the toxic effects of chemotherapy while allowing the treatment to target cancer cells more effectively.

Check Digit Verification of cas no

The CAS Registry Mumber 4007-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,0 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4007-01:
(6*4)+(5*0)+(4*0)+(3*7)+(2*0)+(1*1)=46
46 % 10 = 6
So 4007-01-6 is a valid CAS Registry Number.

4007-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylcarbamothioylsulfanyl)acetic acid

1.2 Other means of identification

Product number -
Other names S-Dimethylthiocarbamoyl-thioglykolsaeure

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:4007-01-6 SDS

4007-01-6Relevant articles and documents

Hapten synthesis for the development of a competitive inhibition enzyme-immunoassay for thiram

Gueguen,Boisde,Queffelec,Haelters,Thouvenot,Corbel,Nodet

, p. 4492 - 4499 (2007/10/03)

An enzyme-linked immunosorbent assay (ELISA) was developed for the fungicide thiram. Two types of haptens were synthesized. The first type exhibits the two symmetrical N-alkyl dithiocarbamate patterns of thiram with a spacer arm linked to one of the N-methyl terminal group. The second type exhibits one of the two symmetrical N-alkyl dithiocarbamate patterns of thiram with a variable-length spacer arm linked to one sulfur atom. Polyclonal antibodies suitable for thiram detection were obtained from immunization with an hapten of the first type, while haptens of the second type were used as coating antigens to develop a competitive ELISA against thiram. The IC50 value for thiram was estimated to be 0.24 μg/mL, with a detection limit of 0.03 μg/mL. The assay seems to be thiram-specific since no or little cross-reaction with other dithiocarbamates were observed.

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