40716-42-5 Usage
Description
[R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide is a complex organic compound with a unique molecular structure that features a hydroxyl group, amide linkage, and a long-chain hydrocarbon tail. This molecule is characterized by its amphiphilic nature, which allows it to interact with both polar and nonpolar substances, making it versatile in various applications.
Uses
Used in Personal Care Industry:
[R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide is used as an emulsifier for its lubricating, wetting, and softening properties. It helps to blend and stabilize formulations, making it an essential component in the creation of personal care products such as creams, lotions, and shampoos.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide can be utilized as a component in drug delivery systems. Its amphiphilic properties enable it to facilitate the transport and absorption of drugs, potentially improving their bioavailability and efficacy.
Used in Cosmetics Industry:
[R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide is used as a foam booster and formula stabilizer when blended with anionic surfactants such as lauryl sulfates. This application is particularly relevant in the development of cosmetics, where foaming and consistency are important factors in product performance and user experience.
Used in Lubricant Formulations:
Due to its lubricating properties, [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide can be employed in the formulation of lubricants for various industrial applications, including automotive, mechanical, and manufacturing processes. Its ability to reduce friction and wear can contribute to improved performance and longevity of machinery and equipment.
Used in Textile Industry:
In the textile industry, [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide can be used as a softening agent to improve the手感 (hand feel) and texture of fabrics. Its wetting properties can also aid in the dyeing and finishing processes, ensuring even distribution of dyes and treatments for consistent color and quality.
Overall, [R-(Z)]-12-hydroxy-N,N-bis(2-hydroxyethyl)-9-octadecenamide is a versatile compound with a wide range of applications across different industries, thanks to its unique chemical properties and ability to interact with various substances.
Check Digit Verification of cas no
The CAS Registry Mumber 40716-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,1 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40716-42:
(7*4)+(6*0)+(5*7)+(4*1)+(3*6)+(2*4)+(1*2)=95
95 % 10 = 5
So 40716-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H43NO4/c1-2-3-4-11-14-21(26)15-12-9-7-5-6-8-10-13-16-22(27)23(17-19-24)18-20-25/h9,12,21,24-26H,2-8,10-11,13-20H2,1H3/b12-9-/t21-/m1/s1
40716-42-5Relevant articles and documents
Synthesis and characterization of ricinoleamide-based polyurethane
Kashif, Mohammad,Sharmin, Eram,Zafar, Fahmina,Ahmad, Sharif
, p. 1989 - 1996 (2011)
Ricinus communis (RC) oil-based materials are currently receiving increasing attention because of economic and environmental concerns. In the present work, RC oil - a natural triol has been utilized for the development of an advanced polymeric material - poly(urethanericinoleamide) (PUR) through very simple synthesis and curing strategy, omitting derivatization steps or side reactions, chain extenders and crosslinkers. The synthesis of PUR was carried out in two steps. The first step is the introduction of an amide group in the RC oil (89.5% ricinoleic acid) via base catalyzed amidation, which results in N, N-bis (2-hydroxyethyl) ricinoleamide (HERA). The second step is urethanation of HERA by the reaction of toluene-2,4-diisocyanate (TDI) in minimal possible organic solvent by one-shot technique, which results in the formation of polyurethane along with amide linkages. The physico-chemical and spectral studies (FT-IR, 1H-NMR and 13C-NMR techniques) confirm these two reactions and the structure of PUR. The resin was cured at ambient temperature without any cross linker. Solubility of the resin was investigated in different polar and non-polar solvents. Thermo-gravimetric analysis (TGA)/differential thermal analysis (DTA) and Differential Scanning Calorimetry (DSC) were used to determine the thermal stability and curing behavior of PUR. An ambient cured ricinoleamide modified polyurethane resin exhibited thermal resistance up to 200-220 °C. AOCS 2011.
