Welcome to LookChem.com Sign In|Join Free
  • or
Cyclohexanol, sodium salt is a white to off-white solid chemical compound formed by the reaction of cyclohexanol with sodium hydroxide. It is soluble in water and alcohol and exhibits a wide range of applications due to its surfactant and emulsifying properties.

22096-22-6

Post Buying Request

22096-22-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

22096-22-6 Usage

Uses

Used in Detergent and Cleaning Agents Industry:
Cyclohexanol, sodium salt is used as a surfactant and emulsifier for its ability to reduce surface tension and stabilize mixtures of oil and water, enhancing the cleaning and lathering properties of detergents and cleaning agents.
Used in Personal Care Products Industry:
Cyclohexanol, sodium salt is used as an emulsifying agent in personal care products such as creams, lotions, and shampoos to help blend ingredients and maintain a uniform texture, ensuring product stability and effectiveness.
Used in Organic Synthesis:
Cyclohexanol, sodium salt serves as an intermediate in the synthesis of other organic compounds, contributing to the production of various chemical products and pharmaceuticals.
Used in Pharmaceutical and Healthcare Industries:
Cyclohexanol, sodium salt may be utilized for its potential antimicrobial properties, making it a candidate for applications in the pharmaceutical and healthcare sectors, such as disinfectants and sanitizers.

Check Digit Verification of cas no

The CAS Registry Mumber 22096-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22096-22:
(7*2)+(6*2)+(5*0)+(4*9)+(3*6)+(2*2)+(1*2)=86
86 % 10 = 6
So 22096-22-6 is a valid CAS Registry Number.

22096-22-6SDS

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 sodium cyclohexanolate

1.2 Other means of identification

Product number -
Other names cyclohexanol sodium salt

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:22096-22-6 SDS

22096-22-6Relevant academic research and scientific papers

Reversible Hydrogen Uptake/Release over a Sodium Phenoxide–Cyclohexanolate Pair

Yu, Yang,He, Teng,Wu, Anan,Pei, Qijun,Karkamkar, Abhijeet,Autrey, Tom,Chen, Ping

, p. 3102 - 3107 (2019/01/04)

Hydrogen uptake and release in arene–cycloalkane pairs provide an attractive opportunity for on-board and off-board hydrogen storage. However, the efficiency of arene–cycloalkane pairs currently is limited by unfavorable thermodynamics for hydrogen release. It is shown here that the thermodynamics can be optimized by replacement of H in the -OH group of cyclohexanol and phenol with alkali or alkaline earth metals. The enthalpy change upon dehydrogenation decreases substantially, which correlates with the delocalization of the oxygen electron to the benzene ring in phenoxides. Theoretical calculations reveal that replacement of H with a metal leads to a reduction of the HOMO–LUMO energy gap and elongation of the C?H bond in the α site in cyclohexanolate, which indicates that the cyclohexanol is activated upon metal substitution. The experimental results demonstrate that sodium phenoxide–cyclohexanolate, an air- and water-stable pair, can desorb hydrogen at ca. 413 K and 373 K in the solid form and in an aqueous solution, respectively. Hydrogenation, on the other hand, is accomplished at temperatures as low as 303 K.

Preparation method for low residual granular sodium alkoxide or potassium alcoholate

-

Paragraph 0055-0046, (2017/01/17)

The invention provides a preparation method for low residual granular sodium alkoxide or potassium alcoholate. The method includes using sodium or potassium and alcohol as raw materials, mixing the mixture with a solvent, reacting in inert gas atmosphere by using a microwave heating method, and removing the residual alcohol and solvent in the presence of microwave after the reaction to get the granular sodium alkoxide or potassium alcoholate. The microwave frequency is 2450 +/- 50 MHz. The method can prepare sodium alkoxide or potassium alcoholate with low residual solvent, and the prepared sodium alkoxide or potassium alcoholate is large granular solid, so that the development from powdered product to granular product can be realized, and the problems of residual solvent and potential risk troubled human for a long time can be overcome.

Spiro Compounds As NPY Y5 Receptor Antagonists

-

Page/Page column 50, (2009/08/18)

The present invention relates to novel compounds of formula (I), or a pharmaceutically acceptable salt thereof, wherein R is an aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano;Z1 is H, C1-C4 alkyl or F;Z is CH2, CH(C1-C4 alkyl), C(C1-C4 alkyl)2 or a bond;A is a 6-10 membered aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; or —C(═O)—X; or —O(CH2)0-1R1;B is hydrogen or is a 5-6 membered heteroaryl, or a 4-6 membered heterocycle, or phenyl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, hydroxyl, cyano; A and B being linked via any atom;R1 is —(C1-C4)alkyl(C1-C4)alkoxy; or C3-C8 cycloalkyl; or R1 is an aryl or heteroaryl, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano; or R1 is a 4-6 membered heterocycle, which may be substituted by one or more: halogen, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkoxy, cyano;X is OR2 or NR3R4;R2 is C1-C4 alkyl;R3 is hydrogen or together with R4 and the nitrogen form a 5-6 saturated membered ring;R4 is C3-C8 cycloalkyl; processes for their preparation, intermediates used in these processes, pharmaceutical compositions containing them and their use in therapy, as NPY Y5 receptor antagonists and as agents for the treatment and/or prophylaxis of eating disorders such as a binge eating disorder.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 22096-22-6