79397-78-7

Usage

Uses

Used in Cleaning Agents and Detergents:
(S)-3,7-dimethyloctyl 4-methylbenzenesulfonate is used as a surfactant and emulsifier for enhancing the cleaning efficiency and effectiveness of various cleaning agents and detergents. Its ability to reduce surface tension and stabilize mixtures of oil and water makes it a valuable component in these products.
Used in Personal Care Products:
In the personal care industry, (S)-3,7-dimethyloctyl 4-methylbenzenesulfonate is used as an ingredient in the formulation of products such as shampoos, conditioners, and lotions. Its emulsifying properties help create stable and homogenous mixtures, improving the texture and performance of these products.
Used in Industrial Applications:
(S)-3,7-dimethyloctyl 4-methylbenzenesulfonate is also employed in various industrial applications, where it serves as an intermediate in the synthesis of other compounds and materials. Its unique chemical structure and properties make it an essential component in the development of new products and technologies.

Upstream product

• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 68680-98-8 S-(-)-dihydrocitronellol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 137304-94-0 5-[4-((S)-3,7-Dimethyl-octyloxy)-phenyl]-2-octyl-pyrimidine 
• 264906-28-7 ethyl 3-[(S)-3,7-dimethyloctyloxy]benzoate 
• 325770-71-6 (S)-4-(3,7-dimethyloctyloxy)nitrobenzene 
• 325770-72-7 (S)-(+)-4-((3,7-dimethyloctyl)oxy)aniline 
• 325770-73-8 (S)-N-[4-(3,7-dimethyloctyloxy)phenyl]-2,3,4-tris(hexyloxy)-benzalimine 
• 293328-36-6 4-[(3S)-3,7-dimethyloctyloxy]benzoic acid 
• 264906-29-8 3-[(S)-3,7-dimethyloctyloxy]benzoic acid 
• 798567-89-2 methyl 3,4,5-tris[(S)-3,7-dimethyloctyloxy]benzoate 
• 1459809-76-7 C₄₅H₇₁NO₄ 
• 798567-90-5 3,4,5-tris(((S)-3,7-dimethyloctyl)oxy)benzoic acid 

Relevant academic research and scientific papers

The Impact of Chiral Citronellyl-Functionalization on Indolenine and Anilino Squaraine Thin Films

The impact on chiral aggregation in solution processed and thermally annealed thin films of two indolenine and one anilino squaraines with chiral (S)-citronellyl functionalization at the nitrogen of the squaraine backbone is investigated. A pseudo polymor

Long-lived charge-transfer state from B?N frustrated Lewis pairs enchained in supramolecular copolymers

The field of supramolecular polymers is rapidly expanding; however, the exploitation of these systems as functional materials is still elusive. To become competitive, supramolecular polymers must display microstructural order and the emergence of new prop

Disc-like chiral palladium and platinum complexes: Synthesis and mesomorphic properties

ortho-Palladated and -platinated benzalimines are a widely studied novel type of liquid-crystals. These sheet-shaped materials contain two or even four metal atoms and carry eight and twelve flexible side-chains, respectively. Here we present the preparation and mesomorphic properties of dinuclear chiral homologues of such sheet-like compounds. On their own, the chiral members of the dinuclear cyclopalladated series exhibit no liquid-crystalline properties, but show mesophase inductions (Colh-phase) in mixtures with an electron-acceptor, e.g.,2,4,7-trinitroflourenone (TNF). A diplatinated chiral analogue, however, monotropically exhibits the cholesteric nematic discotic (ND/*) type of mesophase. Mixtures of this platinum nematogen with TNF also show the induction of a columnar mesophase (Colh) due to charge-transfer interactions.

Synthesis and structure of poly(phenyl isocyanate)s bearing an optically active alkoxyl group

Novel optically active phenyl isocyanate derivatives (1-6) bearing an (R)-sec-butoxy, (S)-2-methylbutoxy or (S)-3,7-dimethyloctyloxy group at the meta or para position on the phenyl ring were prepared and polymerized with an anionic initiator in tetrahydrofuran (THF). The resulting polymers from 1, 2, 4 and 6 showed much greater specific rotation than that of the corresponding monomers and an intense circular dichroism (CD) band in the main-chain absorption region, indicating that these polymers have a predominantly one-handed helical conformation in solution. On the other hand, the polymers obtained from 3 and 5 showed a much smaller specific rotation than that of the above polymers at room temperature. The polymers from 2 and 5 showed a remarkable change in optical activity with change in temperature, and the specific rotation of the polymers changed from a positive to a negative value with decrease in temperature. The CD band of the polymers in the absorption region due to the main chain changed from a positive to a negative peak with a change in specific rotation. These results indicate that poly-2 and poly-5 undergo a thermally induced helix-helix transition in THF. The temperature for the helix-helix transition of poly-2 was independent of the degree of polymerization. Poly-2 exhibited a reversible helix-helix transition in chloroform and diethyl ether and also in THF, whereas in toluene and dichloromethane such a transition was not observed. Copyright