7706-01-6 Usage
Uses
Used in Polymer and Resin Production:
Methyl ricinelaidate is used as a raw material for the production of polymers and resins, leveraging its thermal stability and chemical resistance to enhance the performance of these materials.
Used in Lubricant Formulation:
It serves as a key ingredient in the formulation of lubricants, where its properties contribute to the efficiency and longevity of the lubricating products.
Used in Coatings, Adhesives, and Plasticizers:
Methyl ricinelaidate is used as an additive in the formulation of coatings, adhesives, and plasticizers, improving their overall performance and adaptability for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, methyl ricinelaidate is utilized for its moisturizing and emollient properties, making it a valuable component in the development of various medicinal products.
Used in Cosmetics Industry:
Similarly, in cosmetics, it is employed to provide moisturization and emollience, contributing to the texture, feel, and effectiveness of cosmetic products.
Check Digit Verification of cas no
The CAS Registry Mumber 7706-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7706-01:
(6*7)+(5*7)+(4*0)+(3*6)+(2*0)+(1*1)=96
96 % 10 = 6
So 7706-01-6 is a valid CAS Registry Number.
7706-01-6Relevant academic research and scientific papers
[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles
Ishmuratov, G. Yu.,Yakovleva,Vydrina,Rubleva,Ishmuratova,Tolstikov
, p. 231 - 233 (2017/07/05)
The reactivities of the keto analogs of methyl ricinolate and its triglyceride with hydrazine hydrate were studied. The ester was found to be inert, which made it possible to synthesize a macrocyclic azine with a side chain hydrazone moiety from a 12-oxo-derivative.
Synthesis of enantiomerically pure 2,3,4,6-tetrasubstituted tetrahydropyrans by Prins-type cyclization of methyl ricinoleate and aldehydes
Biermann, Ursula,Luetzen, Arne,Metzger, Juergen O.
, p. 2631 - 2637 (2007/10/03)
The AlCl3-catalyzed Prins-type cyclization of methyl ricinoleate (1), an enantiomerically pure renewable compound, with aldehydes such as heptanal (2a), isobutyraldehyde (2b), pivaldehyde (2c) and benzaldehyde (2d) is a simple reaction for the diastereoselective synthesis of enantiomerically pure 2,3,6-trialkyl-substituted 4-chlorotetrahydropyrans. The respective 4-hydroxytetrahydropyrans are obtained e.g. with aldehydes 2a and 2d using montmorillonite KSF/O as the catalyst. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.
