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2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one, commonly referred to as CTC, is a synthetic organic compound belonging to the class of halogenated aryl compounds. It is characterized by its unique chemical structure, which includes a dihydro-isoindole core with four chlorine atoms and an imino group. 2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one is widely recognized for its versatile applications in various industries, primarily as a chemical intermediate in the production of dyes, pigments, and pharmaceuticals. Additionally, CTC is known for its potent antimicrobial and disinfectant properties, which have led to its use in bactericides and algaecides. However, due to its high toxicity and potential environmental impact, CTC has become a subject of regulation and environmental monitoring in many countries. Its use necessitates careful handling and disposal to mitigate any adverse effects on human health and the environment.

5358-09-8

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5358-09-8 Usage

Uses

Used in Chemical Intermediates Industry:
2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one is used as a chemical intermediate for the production of dyes, pigments, and pharmaceuticals. Its unique chemical structure and reactivity make it a valuable component in the synthesis of various organic compounds.
Used in Antimicrobial Applications:
In the field of antimicrobial agents, 2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one is used as a disinfectant and bactericide due to its strong antimicrobial properties. It is effective against a wide range of microorganisms, making it a common ingredient in products designed to control microbial growth and prevent infections.
Used in Algaecide Formulations:
2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one is used as an active ingredient in algaecides for the control of algae growth in various settings, such as water treatment facilities, swimming pools, and industrial cooling systems. Its effectiveness in inhibiting algae growth helps maintain water quality and prevent the formation of harmful algal blooms.
Environmental Monitoring and Regulation:
Due to the high toxicity and potential environmental impact of 2,3-Dihydro-4,5,6,7-tetrachloro-3-imino-1H-isoindole-1-one, it has become a target for regulation and environmental monitoring in many countries. This involves the development of guidelines and standards for its use, handling, and disposal to minimize its adverse effects on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 5358-09-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,5 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5358-09:
(6*5)+(5*3)+(4*5)+(3*8)+(2*0)+(1*9)=98
98 % 10 = 8
So 5358-09-8 is a valid CAS Registry Number.

5358-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-4,5,6,7-tetrachloroisoindol-1-one

1.2 Other means of identification

Product number -
Other names tetrachloro-3-iminoisoindolin-1-one

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:5358-09-8 SDS

5358-09-8Upstream product

5358-09-8Downstream Products

5358-09-8Relevant academic research and scientific papers

Preparation of tetrachloro-3-iminoisoindolin-1-one

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, (2008/06/13)

Tetrachloro-3-iminosisoindolin-1-one (I) or its alkali metal salt (Ia) is prepared by reacting tetrachloro-ortho-phthalodinitrile with lithium hydroxide, sodium hydroxide and/or potassium hydroxide in substantially anhydrous tert-butanol and, if desired, liberating (I) from (Ia) by means of a dilute acid.

Process for producing phthalimido derivatives

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, (2008/06/13)

A process for producing a 3-iminohaloisoindoline-1-one which comprises treating a halophthalodinitrile with ammonia and/or an organic amine together with hydrogen peroxide in a mixed reaction medium comprising water and an organic solvent.

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