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3.3'.4.4'-Tetra Aminobenzophenone, also known as TAABP, is a chemical compound characterized by its molecular formula C13H14N4O. It is a yellow powder that exhibits high stability and non-volatility, with solubility in organic solvents but not in water. TAABP is utilized in various applications due to its unique properties, including the manufacturing of dyes and pigments, photoprotective and antistatic agents, and materials for electronic devices. Additionally, it serves as a fluorescent probe in biological studies. However, it is classified as a hazardous chemical, necessitating careful handling and adherence to proper safety measures.

5007-67-0

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5007-67-0 Usage

Uses

Used in Dye and Pigment Manufacturing:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a key component in the production of dyes and pigments for its ability to impart color and stability to these substances.
Used in Photoprotective Agents:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a photoprotective agent to safeguard materials from the damaging effects of ultraviolet radiation, thereby extending their lifespan and performance.
Used in Antistatic Agents:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as an antistatic agent to reduce the buildup of static electricity on surfaces, which is crucial in industries such as electronics and textiles to prevent damage to sensitive components or materials.
Used in Electronic Device Production:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a material in the production of electronic devices, leveraging its stability and properties to enhance the performance and reliability of these devices.
Used in Biological Studies as a Fluorescent Probe:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used as a fluorescent probe in biological research, allowing for the visualization and tracking of cellular processes and components due to its fluorescent properties.
Used in Safety and Handling Procedures:
3.3'.4.4'-TETRA AMINOBENZOPHENONE is used in the development of safety and handling procedures due to its classification as a hazardous chemical, ensuring that workers and the environment are protected during its use and disposal.

Check Digit Verification of cas no

The CAS Registry Mumber 5007-67-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5007-67:
(6*5)+(5*0)+(4*0)+(3*7)+(2*6)+(1*7)=70
70 % 10 = 0
So 5007-67-0 is a valid CAS Registry Number.

5007-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3.3.4.4-Tetra Aminobenzophenone

1.2 Other means of identification

Product number -
Other names bis(3,4-diaminophenyl)methanone

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:5007-67-0 SDS

5007-67-0Relevant academic research and scientific papers

Studies in antiparasitic agents: Part 20 - Synthesis of probenzimidazoles, benzimidazoles and purimidobenzimidazoles as possible anthelmintics

Srivastava, Ravi P.,Singh, Sudhir K.,Abuzar, Syed,Sharma, Satyavan,Gupta, Suman,et al.

, p. 1035 - 1044 (2007/10/02)

A series of tetrasubstituted benzophenones (1-35) have been synthesized as probenzimidazoles.Some 2,5-disubstituted benzimidazoles (36-39 and 43-61) and pyrimidobenzimidazoles (40-42) have also been prepared.Of these compounds 4, 5, 15, 27, 29, 30, and 51 exhibit 100percent antihookworm activity against A. ceylanicum in hamsters at an oral dose of 250 mg/kg*3 while compounds 3, 4, 26-30 cause 100percent elimination of tapeworms, H. nana at a dose of 250 mg/kg.Compound 4 kills 90percent of the microfilariae of L. carinii at an intraperitoneal dose of 30 mg/kg*5.Another compound, 48 shows 6 4-78percent microfilaricidal and 38-62percent macrofilaricidal action against L. carinii and B. malayi at a dose of 50 mg/kg*5.

Synthesis and Anthelmintic Activity of Bisbenzimidazole-2-carbamates

Viswanathan, N.,Joshi, B. S.,Gawad, D. H.,Gokhale, U. B.,Sidhaye, A. R.,Rajasekariah, G. R.

, p. 730 - 732 (2007/10/02)

The synthesis of bisbenzimidazole-2-carbamates (1-6) linked directly or by a one-atom bridge (CH2, CO, O, SO2, or S) at the 5 positions is described.Compound (4) shows interesting anthelmintic activity.

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