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Phosphonic acid, cyclohexyl-, dibutyl ester is an ester derivative of cyclohexyl phosphonic acid, a type of organophosphorus compound. It is an industrial intermediate and specialty chemical known for its versatile applications across various industries.

1085-92-3

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1085-92-3 Usage

Uses

Used in Plasticizer Applications:
Phosphonic acid, cyclohexyl-, dibutyl ester is used as a plasticizer in the production of polymers, resins, and adhesives. It enhances the flexibility and workability of these materials, improving their performance in various applications.
Used in Flame Retardant Applications:
This chemical compound is used as a flame retardant, providing fire resistance to materials and reducing the risk of fire-related incidents. It is particularly useful in industries where fire safety is a critical concern.
Used in Water Treatment Applications:
Phosphonic acid, cyclohexyl-, dibutyl ester is used as an anti-scaling agent in water treatment applications. It helps prevent the formation of scale deposits in water systems, ensuring efficient operation and reducing maintenance requirements.
Used in Lubricant Additive Applications:
As a lubricant additive, this chemical compound improves the performance of lubricants, enhancing their ability to reduce friction and wear in mechanical systems. It is particularly useful in industries where machinery operates under high loads and temperatures.
Used in Agricultural Formulations:
Phosphonic acid, cyclohexyl-, dibutyl ester is used in agricultural formulations to enhance the effectiveness of pesticides and other agrochemicals. It helps improve the delivery and absorption of these chemicals, increasing their efficacy in crop protection.
Used in Chemical Synthesis Industry:
Phosphonic acid, cyclohexyl-, dibutyl ester is used as a chemical intermediate in the synthesis of various specialty chemicals and pharmaceuticals. Its unique properties make it a valuable building block for the development of new compounds with specific applications.
However, it is important to handle Phosphonic acid, cyclohexyl-, dibutyl ester with care, as it is toxic and may cause skin and eye irritation upon contact. Proper safety measures should be taken during its use to minimize potential health risks.

Check Digit Verification of cas no

The CAS Registry Mumber 1085-92-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1085-92:
(6*1)+(5*0)+(4*8)+(3*5)+(2*9)+(1*2)=73
73 % 10 = 3
So 1085-92-3 is a valid CAS Registry Number.

1085-92-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name dibutoxyphosphorylcyclohexane

1.2 Other means of identification

Product number -
Other names Cyclohexyl-phosphonsaeure-dibutylester

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:1085-92-3 SDS

1085-92-3Downstream Products

1085-92-3Relevant academic research and scientific papers

Extraction of actinides by Tri-n-butyl phosphate derivatives: Effect of substituents

Annam, Suresh,Gopakumar, Gopinadhanpillai,Brahmmananda Rao,Sivaraman,Sivaramakrishna, Akella,Vijayakrishna, Kari

, p. 123 - 132 (2017/09/18)

Tri-n-butyl phosphate (TBP) is most extensively used extractant in the nuclear fuel cycle. The present work investigates the effect of substituents and their role in the basicity of organophosphorus extractant on the uptake of actinides. In this connection, we have synthesized six different analogues of TBP by altering one of its butoxy group. The synthesized TBP derivatives were well characterized and evaluated for their solvent extraction behavior towards U(VI), Th(IV), Pu(IV) and Am(III), as well as acid uptake as a function of nitric acid ranging from 0.01 to 6 M and the data provides the comparison of their extraction behavior with that of 30% (1.1 M) tri-n-butyl phosphate under identical conditions. It was observed that distribution coefficient values strongly depend on the nature and size of the substituents. The presence of electron donating groups enhances the uptake of the actinides and the distribution coefficient values were significantly larger as compared to that of TBP. In addition, the effect of sodium nitrate on the extraction of uranium and enthalpy of extraction were also studied and revealed that the extraction process was exothermic.

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