2432-87-3 Usage
Description
SEBACIC ACID DI-N-OCTYL ESTER, also known as Dioctyl sebacate, is a synthetic organic compound that belongs to the ester class. It is characterized by its liquid state, with a pour point of -55°C and a boiling point of 248°C at 4 mmHg. SEBACIC ACID DI-N-OCTYL ESTER is known for its plasticizing properties, making it a versatile material in various industries.
Uses
Used in Plastic Industry:
SEBACIC ACID DI-N-OCTYL ESTER is used as a plasticizer for its ability to increase the flexibility, workability, and processability of plastics. It is particularly useful in the production of various types of polymers, such as polyvinyl chloride (PVC), where it helps to improve the material's overall performance and durability.
Used in Lubricant Industry:
In the lubricant industry, SEBACIC ACID DI-N-OCTYL ESTER is used as an additive to enhance the performance of lubricants. Its liquid state and low pour point make it an effective component in formulating lubricants with improved low-temperature properties, ensuring smooth operation and reduced wear under cold conditions.
Used in Personal Care Industry:
SEBACIC ACID DI-N-OCTYL ESTER is also utilized in the personal care industry, where it serves as an ingredient in various cosmetic and skincare products. Its compatibility with the skin and ability to improve the texture and feel of formulations make it a valuable component in creams, lotions, and other skincare products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, SEBACIC ACID DI-N-OCTYL ESTER is employed as an excipient in the formulation of various drug delivery systems. Its plasticizing properties help to improve the stability, bioavailability, and overall performance of medications, ensuring their effectiveness and safety for patients.
Flammability and Explosibility
Notclassified
Check Digit Verification of cas no
The CAS Registry Mumber 2432-87-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2432-87:
(6*2)+(5*4)+(4*3)+(3*2)+(2*8)+(1*7)=73
73 % 10 = 3
So 2432-87-3 is a valid CAS Registry Number.
InChI:InChI=1/C26H50O4/c1-3-5-7-9-15-19-23-29-25(27)21-17-13-11-12-14-18-22-26(28)30-24-20-16-10-8-6-4-2/h3-24H2,1-2H3
2432-87-3Relevant articles and documents
Biomass-derived dibasic acids to diesters with inorganic ligand-supported catalyst: synthesis, optimization, characterization
Chen, Zhe,Han, Sheng,Lu, Deli,Xu, Yumeng
, (2021/08/23)
Several attempts have been made to obtain aliphatic dicarboxylic diesters from esterification reaction to develop the biomass-derived platform molecules and green manufacturing processes. In this paper, Na3(H2O)6[AlMo6O18(OH)6], an Anderson-type polyoxometalate, firstly, was reported as a catalyst for diester synthesis from dicarboxylic acid to diester which showed an well productivity and selectivity characterized by 1H and 13C. Response surface methodology (RSM) integrated with the desirability function approach was used to determine the best operative conditions, and the optimal reaction parameters for maximum dipropyl succinate yield (77 ± 2.5%) were identified as 1.19?mol.% catalyst loading, 4.9:1 propanol/succinic acid ratio, 113?°C, and 9.6?h. Three batches of tests were carried for catalyst recycling with 78–75% yield even after 6 cycles of esterification. In addition, the substrate carbon chain was increased for investigation of substrate scope achieving satisfactory results and all products were characterized by 1H and 13C nuclear magnetic resonance spectroscopy.
SKIN EXTERNAL PREPARATIONS AND COSMETICS
-
, (2010/12/29)
An object of the present invention is to provide skin external preparations and cosmetics which contain a branched acyl carnitine and have excellent formulation stability. A skin external preparation of the present invention includes a carnitine derivative represented by the following Formula (1) and/or a carnitine derivative salt represented by the following Formula (2), and an amphoteric surfactant. In Formula (1), R1 and R2 are each independently a C1-18 optionally branched, saturated or unsaturated aliphatic hydrocarbon group. In Formula (2), R1 and R2 are the same as in Formula (1), X? is a specific anion and Y+ is a specific cation.
