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4-(4-Propylcyclohexyl)cyclohexanone, also known as PCHP, is a synthetic chemical compound with the molecular formula C18H30O. It is a member of the cyclohexanone family, characterized by its clear, colorless appearance and a distinctive odor. PCHP is insoluble in water but readily soluble in organic solvents. 4-(4-Propylcyclohexyl)cyclohexanone is known for its low toxicity, contributing to its relative safety in industrial applications, although proper handling and storage are still essential to mitigate any potential risks.

87625-09-0

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87625-09-0 Usage

Uses

Used in Lubricant Industry:
4-(4-Propylcyclohexyl)cyclohexanone is used as a lubricant for its ability to reduce friction between surfaces, which is crucial in various mechanical applications to prevent wear and tear and to enhance the longevity of machinery.
Used in Plasticizer Industry:
In the plastics industry, 4-(4-Propylcyclohexyl)cyclohexanone serves as a plasticizer, helping to increase the flexibility and workability of plastic materials. This property is particularly valuable in the manufacturing of certain types of plastics that require enhanced flexibility for specific applications.
Given the provided materials, there are no specific applications mentioned for industries other than lubricants and plasticizers. However, the compound's properties of being a synthetic chemical, its solubility in organic solvents, and its low toxicity suggest that it may have potential uses in other areas such as chemical synthesis, coatings, or adhesives, depending on further research and development in those fields.

Check Digit Verification of cas no

The CAS Registry Mumber 87625-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,2 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 87625-09:
(7*8)+(6*7)+(5*6)+(4*2)+(3*5)+(2*0)+(1*9)=160
160 % 10 = 0
So 87625-09-0 is a valid CAS Registry Number.

87625-09-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4'-Propyl-1,1'-bi(cyclohexyl)-4-one

1.2 Other means of identification

Product number -
Other names 4-(TRANS-4'-N-PENTYLCYCLOHEXYL)CYCLOHEXANONE

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:87625-09-0 SDS

87625-09-0Relevant academic research and scientific papers

Synthesis method of 4-substituent cyclohexanone liquid crystal intermediate

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Paragraph 0052; 0054-0055, (2021/05/19)

The invention discloses a synthesis method of a 4-substituent cyclohexanone liquid crystal intermediate, which comprises the following step: carrying out oxidation catalytic reaction on 4-substituent cyclohexanol under the action of trichloroisocyanide urea to obtain the 4-substituent cyclohexanone liquid crystal intermediate. The method is high in reaction selectivity, high in yield, environment-friendly, simple in post-treatment and suitable for industrial production.

Aerobic alcohol oxidation using a PdCl2/N,N-dimethylacetamide catalyst system under mild conditions

Wang, Lian-Yue,Li, Jun,Lv, Ying,Zhang, Heng-Yun,Gao, Shuang

experimental part, p. 3257 - 3263 (2011/10/09)

A new and simple PdCl2/DMA catalytic system for the alcohol oxidation has been developed using molecular oxygen as the sole oxidant under mild conditions. The catalytic system could be reused for three runs without significant loss of catalytic activity. A variety of active and non-active alcohols were oxidized to their corresponding carbonyl compounds in good to excellent yields. Gas-uptake kinetics for the catalytic system was also investigated. The ca. 1:1 molar ratio of O2 uptake to product yield is observed, suggesting the in situ formation of H2O2.

Process for the preparation of cyclohexanones

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, (2008/06/13)

The invention relates to a process for the preparation of cyclohexanones from the corresponding phenols by partial hydrogenation, characterized in that the reaction mixture obtained by means of the hydrogenation is treated with sulfonating agents before the isolation of the cyclohexanone.

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