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3,7-bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine, also known as KM-294, is a chemical compound belonging to the phenothiazine family. It is recognized for its stabilizing properties in various industrial applications, particularly in the manufacturing of polymers, plastics, rubber, and in the formulation of lubricants and oils. Its ability to prevent material degradation due to heat, light, and oxygen exposure makes it a valuable additive in these industries. Furthermore, it has been investigated for its potential as a pharmaceutical agent, with studies suggesting its use as an antipsychotic and antidepressant due to its interaction with dopamine receptors in the brain.

10538-33-7

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10538-33-7 Usage

Uses

Used in Polymer and Plastics Industry:
3,7-bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine is used as a stabilizer to prevent the degradation of polymers and plastics caused by exposure to heat, light, and oxygen, thereby enhancing their durability and longevity.
Used in Rubber Production:
In the rubber industry, 3,7-bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine serves as an antioxidant, which helps to maintain the elasticity and structural integrity of rubber products over time, protecting them from oxidative damage.
Used in Lubricants and Oils Formulation:
As a stabilizer in the formulation of lubricants and oils, 3,7-bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine helps to extend the lifespan of these products by reducing oxidation and wear, thus improving their performance and efficiency.
Used in Pharmaceutical Research:
3,7-bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine is being studied for its potential applications in medicine, particularly as an antipsychotic and antidepressant agent. Its interaction with dopamine receptors in the brain suggests a role in modulating neurotransmission, which could be beneficial for the treatment of certain psychiatric disorders. However, further research is necessary to fully understand its pharmacological properties and therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 10538-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,3 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10538-33:
(7*1)+(6*0)+(5*5)+(4*3)+(3*8)+(2*3)+(1*3)=77
77 % 10 = 7
So 10538-33-7 is a valid CAS Registry Number.
InChI:InChI=1/C28H41NS/c1-25(2,3)17-27(7,8)19-11-13-21-23(15-19)30-24-16-20(12-14-22(24)29-21)28(9,10)18-26(4,5)6/h11-16,29H,17-18H2,1-10H3

10538-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7-bis(2,4,4-trimethylpentan-2-yl)-10H-phenothiazine

1.2 Other means of identification

Product number -
Other names 3,7-Bis(1,1,3,3-tetramethylbutyl)-10H-phenothiazine

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:10538-33-7 SDS

10538-33-7Downstream Products

10538-33-7Relevant academic research and scientific papers

Synthetic method and application of phenothiazine and/or derivative thereof

-

Paragraph 0065, (2016/11/24)

The invention discloses a synthetic method for phenothiazine and/or a derivative thereof. The synthetic method comprises the following steps: mixing diphenylamine and/or a diphenylamine derivative, sulphur and a solid acid catalyst; then subjecting the obtained mixture to full reaction in a protective atmosphere; and then carrying out post-treatment so as to obtain phenothiazine and/or the derivative thereof. The invention also discloses application of phenothiazine and/or the derivative thereof. The synthetic method for phenothiazine and/or the derivative thereof is a safe, energy-saving, green and environment-friendly process which is simple to operate, mild in reaction conditions, short in reaction period, convenient to control, high in process security, low in production energy consumption and high in yield; the prepared phenothiazine and/or the derivative thereof has high purity; water, organic solvents and the like are not needed in the reaction process; post-treatment is simple; raw materials, the solid acid catalyst and the like are widely and easily available and cheap; the solid acid catalyst can be recovered and reused; and the method has low cost and is applicable to large scale production.

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