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2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxy-phenyl)cyclohexyl]phenol is a synthetic organic compound that belongs to the family of phenols and cyclohexyls. It is characterized by the presence of two chlorine atoms, a phenol group, and a cyclohexyl group, which contribute to its unique chemical properties and potential applications.

13168-35-9

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13168-35-9 Usage

Uses

Used in Cosmetics and Personal Care Products:
2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxy-phenyl)cyclohexyl]phenol is used as an additive in cosmetics and personal care products for its antimicrobial properties. It helps to maintain the freshness and cleanliness of these products, preventing the growth of bacteria and other microorganisms that could spoil the products or cause skin irritation.
Used in Industrial Processes:
This chemical compound is also used in various industrial processes as an additive. Its antimicrobial properties can be beneficial in applications where controlling the growth of microorganisms is essential, such as in the production of certain types of plastics or textiles.
Used in Antimicrobial Applications:
2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxy-phenyl)cyclohexyl]phenol is used as an antimicrobial agent in antibacterial soaps and disinfectants. Its ability to inhibit the growth of bacteria makes it a valuable component in these products, helping to maintain a clean and hygienic environment.
Used in Pharmaceutical Research:
Although its use in this area is still under investigation, 2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxy-phenyl)cyclohexyl]phenol has been studied for its potential antioxidant and anti-inflammatory properties. These characteristics could make it a promising candidate for the development of new pharmaceuticals, particularly in the treatment of conditions where inflammation and oxidative stress play a role.
However, it is important to note that the use of 2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxy-phenyl)cyclohexyl]phenol has been controversial due to concerns about its potential toxicity and environmental impact. As a result, its application in various industries is subject to strict regulations and ongoing research to ensure its safety and efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 13168-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,6 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13168-35:
(7*1)+(6*3)+(5*1)+(4*6)+(3*8)+(2*3)+(1*5)=89
89 % 10 = 9
So 13168-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H16Cl4O2/c19-12-6-10(7-13(20)16(12)23)18(4-2-1-3-5-18)11-8-14(21)17(24)15(22)9-11/h6-9,23-24H,1-5H2

13168-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-[1-(3,5-dichloro-4-hydroxyphenyl)cyclohexyl]phenol

1.2 Other means of identification

Product number -
Other names 1,1'-bis(3,5-dichloro-4-hydroxyphenyl)cyclohexane

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:13168-35-9 SDS

13168-35-9Downstream Products

13168-35-9Relevant academic research and scientific papers

Synthesis and spectral study of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids with antimicrobial activity

Bhadja,Parsania

, p. 1699 - 1704 (2012/06/15)

Synthesis of R,R′,4,4′-cyclohexylidene diphenyloxy acetic acids (R,R′=H,CH3and Cl) by dissolving 0.1 mole bisphenols in 0.4 mole sodim hydroxide with drop wise addition of 0.2 mole chloroacetic acid. The reaction mixture refluxed for 4h at 60°C. Phenoxy acids have been confirmed by IR and NMR spectral characterization. The acids are also characterized by their antimicrobial and antifungal activities. The activities have been interpreted in light of bisphenol structures and the nature of substituent(s). The wide scale uses of bisphenol bioactive agents have brought many advantages to the agricultural industries.

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