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Isodecanol is a clear, colorless liquid that belongs to the family of alcohols. It is also known as decyl alcohol and is commonly used in the cosmetics and personal care industry as an emollient, emulsifier, and thickening agent in various products such as lotions, creams, and hair care products. Isodecanol is also used in the production of surfactants, lubricants, and fragrances.
Product List
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Catalog Number | Product Name | Inquiry |
ACM25339177 | Isodecanol | INQUIRY |
ACM93685484 | Isodecanol, mixed esters with C4-6 dicarboxylic acids and heptanol | INQUIRY |
ACM112301 | Decanol, CAS 112-30-1 | INQUIRY |
ACM36729585 | Decanol, CAS 36729-58-5 | INQUIRY |
ACM85995864 | Decanol, branched | INQUIRY |
ACM90342328 | Decanol, branched and linear | INQUIRY |
ACMA00008872 | Decanol Impurities | INQUIRY |
ACMA00008873 | Decanol FCC | INQUIRY |
Isodecanol can be prepared using several methods, including hydroformylation of 1-decene or hydrogenation of isodecyl aldehydes. Here is a general process for preparing isodecanol through the hydrogenation of isodecyl aldehydes:
1. Synthesis of Isodecyl Aldehydes:
Isodecyl aldehydes can be prepared by the hydroformylation of 1-decene using a catalyst such as cobalt carbonyl or rhodium catalyst.
2. Hydrogenation of Isodecyl Aldehydes:
Isodecyl aldehydes are then subjected to hydrogenation in the presence of a hydrogenation catalyst such as nickel, palladium, or platinum. The hydrogenation process converts the aldehydes into the corresponding alcohols, including isodecanol.
3. Distillation and Purification:
The crude isodecanol obtained from the hydrogenation reaction is usually subjected to distillation to separate and purify the isodecanol from other by-products and impurities.
4. Refining and Further Processing:
The purified isodecanol can be further refined through processes such as filtration, solvent extraction, or crystallization to obtain a high-purity product. The final product can be used in various industries such as personal care, household products, and industrial applications.
Overall, the preparation of isodecanol involves several steps, including the synthesis of isodecyl aldehydes and their subsequent hydrogenation to produce the desired product. Careful attention to the reaction conditions and purification steps is essential to ensure the quality and purity of the final isodecanol product.
Nb and Ta were simultaneously extracted from the processed sulfate solution, and the solvent isodecanol (C10H22O) was chosen due to its low availability and cost. In general, the good solubility of isodecanol may be due to its high dipole moment and the presence of electronegative O-H bonds. The molecular formula of isodecanol is {CH3(CH3)CH(CH2)6CH3(OH)}, with a density of 0.841. Alcohols with C8-C12 chain length may be of particular interest as potential extractants for liquid-liquid extraction, with n-octanol exhibiting efficiency comparable to MIBK and TBP in liquid-liquid extraction. The main advantages of isodecanol are its insolubility in water, low volatility, and low risk.
Figure 1. Proposed technical flowsheet for the treated sulfate solution.
Isodecanol has a variety of applications across different industries. Some of the common applications of isodecanol include:
Overall, isodecanol is a versatile ingredient with a wide range of applications in various industries, thanks to its emollient, surfactant, solvent, and dispersing properties.