4007-01-6

Basic information

• Product Name: S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID
• Synonyms: S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID;Dimethylthiocarbamoylthioglycolicacid;2-(dimethylcarbamothioylsulfanyl)acetic acid;2-(dimethylcarbamothioylsulfanyl)ethanoic acid;2-(dimethylthiocarbamoylthio)acetic acid;{[(Dimethylamino)carbonothioyl]thio}acetic acid;S-(N,N-Dimethylthiocarbamoyl)thioglycolic Acid;S-(N,N-DIMETHYLTHIOCARBAMOYL)MERCAPTOACETIC ACID
• CAS NO: 4007-01-6
• Molecular Formula: C₅H₉NO₂S₂
• Molecular Weight: 179.26
• Mol File: 4007-01-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 148.0 to 152.0 °C
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID(4007-01-6)
• EPA Substance Registry System: S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID(4007-01-6)

Safety Data

• Hazardous Substances Data: 4007-01-6(Hazardous Substances Data)

Usage

General Description

S-(N,N-DIMETHYLTHIOCARBAMOYL)THIOGLYCOLIC ACID, also known as ADTGA, is a chemical compound with the molecular formula C6H11NO2S2. It is a thiol-based compound that is commonly used in the production of metal chelating agents, pharmaceuticals, and as a building block for organic synthesis. ADTGA is known for its strong chelating and binding properties, making it useful in various industrial and scientific applications. It is also used as a corrosion inhibitor in industrial processes and as an ingredient in personal care products and cosmetics. Additionally, it has potential applications in the treatment of metal poisoning and as a chemoprotective agent in medical research.

Upstream product

• 79-08-3 bromoacetic acid 
• 128-04-1 sodium dimethyldithiocarbamate 
• 3926-62-3 sodium monochloroacetic acid 
• 75-15-0 carbon disulfide 
• 124-40-3 dimethyl amine 
• 79-11-8 chloroacetic acid 
• 128-03-0 potassium dimethyldithiocarbamate 
• 20821-67-4 S-Aethoxycarbonylmethyl-N,N-dimethyl-dithiocarbamat 
• 61540-35-0 S-(Dimethylthiocarbamoyl)thioglycolonitrile 
• 79-04-9 chloroacetyl chloride 

Downstream Products

• 135327-50-3 triphenyltin dimethyldithiocarbamylacetate 
• 135327-46-7 tri-cyclohexyltin dimethyldithiocarbamate 
• 816-75-1 S-Carbamoylmethyl-N,N-dimethyl-dithiocarbamat 
• 6926-58-5 4,4-dimethylthiosemicarbazide 
• 70031-49-1 dimethylthiocarbamoylsulfanyl-acetic acid butyl ester 
• 20821-67-4 S-Aethoxycarbonylmethyl-N,N-dimethyl-dithiocarbamat 
• 27888-12-6 dimethylthiocarbamoylsulfanyl-acetic acid methyl ester 

Relevant articles and documents

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

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.