43035-11-6

Basic information

• Product Name: 2-amino-5-dimethylaminophenylthiosulphonic acid
• Synonyms: 2-amino-5-dimethylaminophenylthiosulphonic acid
• CAS NO: 43035-11-6
• Molecular Weight: 248.327
• Mol File: 43035-11-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 2-amino-5-dimethylaminophenylthiosulphonic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-5-dimethylaminophenylthiosulphonic acid(43035-11-6)
• EPA Substance Registry System: 2-amino-5-dimethylaminophenylthiosulphonic acid(43035-11-6)

Safety Data

• Hazardous Substances Data: 43035-11-6(Hazardous Substances Data)

Upstream product

• 138-89-6 p-dimethylaminonitrosobenzene 
• 7732-18-5 water 
• 64-19-7 acetic acid 
• 99-98-9 4-amino-N,N-dimethylaniline 
• 7664-93-9 sulfuric acid 
• 2836-03-5 N,N-dimethyl-1,2-phenylenediamine 
• 121-69-7 N,N-dimethyl-aniline 
• 536-47-0 N,N-dimethyl-1,4-phenylenediamine sulfate 
• 57842-97-4 N,N-dimethyl-p-phenylenediamine,radical ion[1+]; bromide 

Downstream Products

• 79138-22-0 N,N-dimethyl-1,3-benzothiazol-6-amine 
• 43000-36-8 4-(6-dimethylamino-benzothiazol-2-yl)-phenol 
• 10205-77-3 [2-(4-dimethylamino-phenyl)-benzothiazol-6-yl]-dimethyl-amine 
• 101632-41-1 {2-[4-(2-diethylamino-ethoxy)-phenyl]-benzothiazol-6-yl}-dimethyl-amine 
• 15967-15-4 (4-(2-(thiosulfate)-4-(dimethylamino)-phenylimino)-cyclohex-2,5-dienylidene)-N,N-dimethyl ammonium 
• 55565-65-6 2-(6-dimethylamino-benzothiazol-2-yl)-phenol 
• 10205-73-9 6-dimethylamino-2-phenylbenzothiazole 
• 43036-43-7 2-amino-5-dimethylamino-phenyl mercaptan 
• 2941-73-3 6-(N,N-dimethylamino)-2-methylbenzothiazole 
• 64334-41-4 N⁶,N⁶-dimethyl-benzothiazole-2,6-diamine 
• 1334305-29-1 3-amino-7-(dimethylamino)-2-phenylphenothiazinium hydrogensulphate 
• 26283-09-0 methylene Blue; zinc chloride-double salt 

Relevant articles and documents

Molecular probe derived from calcium-sensitive receptor protein antagonist and application of molecular probe in parathyroid gland resection surgery

The invention discloses a molecular probe derived from a calcium-sensitive receptor protein antagonist and application of the molecular probe in parathyroid gland resection surgery. The molecular probe is specifically a molecular probe which is derived fr

A preparation method of methylene blue

The invention discloses a preparation method of methylene blue, and belongs to the technical field of intermediate synthesis in fine chemical engineering. The preparation method comprises the following steps: in a condensed hydrochloric acid solution, carrying out nitrosation reactions between sodium nitrite and N,N-dimethylaniline so as to obtain an intermediate namely p-nitroso-N,N-dimethylaniline; subjecting p-nitroso-N,N-dimethylaniline to hydrogenation reduction to prepare p-amino-N,N-dimethylaniline; oxidizing p-amino-N,N-dimethylaniline, then adding sodium thiosulfate to carry out addition reactions to prepare 2-amino-5-dimethylaminophenyl thiosulfonic acid, adding N,N-dimethylaniline into 2-amino-5-dimethylaminophenyl thiosulfonic acid to carry out oxidative condensation reactions to generate bis(4-dimethylaminophenyl) thiosulfonic acid; and making bis(4-dimethylaminophenyl) thiosulfonic acid carry out ring-closing reactions to obtain methylene blue. The provided preparation method has the advantages of high product purity, simple technology flow, low manufacture cost, suitability for industrial production, easily-available raw materials, and little pollution to the environment.

Phenothiazinium photosensitisers XI. Improved toluidine blue photoantimicrobials

The phenothiazinium derivative toluidine blue O (TBO) is widely employed as a photoantimicrobial agent in clinical trialling, particularly in dentistry. However, its activity against a range of pathogenic microbial species is not significantly different t