693-55-0

Usage

Uses

Used in the Fragrance Industry:
Ethyl hydrogen sebacate is used as a scent enhancer in perfumes and cosmetic products, providing a sweet, fruity aroma that enhances the overall sensory experience of these products.
Used in the Flavor Industry:
Ethyl hydrogen sebacate is used as a flavoring agent in food products, imparting a sweet, fruity taste that enhances the flavor profile of various food items.
Used in the Plastics Industry:
Ethyl hydrogen sebacate is used in the production of plasticizers, which are additives that improve the flexibility and durability of plastics, making them more suitable for various applications.
Used in the Chemical Synthesis Industry:
Ethyl hydrogen sebacate is used in the synthesis of other chemicals, such as pharmaceuticals and agricultural products, contributing to the development of new and innovative products in these fields.
Overall, ethyl hydrogen sebacate plays a vital role in various industries, particularly in enhancing the sensory qualities of consumer products, making them more appealing to users.

InChI:InChI=1/C12H22O4/c1-2-16-12(15)10-8-6-4-3-5-7-9-11(13)14/h2-10H2,1H3,(H,13,14)

Upstream product

• 79-21-0 peracetic acid 
• 692-86-4 ethyl 10-undecenenoate 
• 111-20-6 1,10-decanedioic acid 
• 64-17-5 ethanol 
• 110-40-7 diethyl sebacate 
• 106-79-6 dimethyl sebacate 
• 108-55-4 glutaric anhydride, 
• 25542-62-5 6-bromo-hexanoic acid ethyl ester 

Downstream Products

• 111-20-6 1,10-decanedioic acid 
• 110-40-7 diethyl sebacate 
• 1472-90-8 diethyl octadecanedioate 
• 14811-95-1 eicosa-1,19-diene 
• 18281-04-4 ethyl nonadecanoate 
• 1472-93-1 dimethyl 1,18-octadecanedioate 
• 28598-81-4 ethyl 9-bromononanoate 
• 6946-46-9 9-ethoxycarbonylnonanoic acid chloride 
• 234081-96-0 10-(tert-butoxy)-10-oxodecanoic acid 
• 64701-47-9 10-(1-pyrenyl)decanoic acid 
• 69267-34-1 10-Hydroxy-10-phenyl-decanoic acid 
• 112-47-0 1,10-Decanediol 
• 15786-31-9 diethyl hexadecanedioate 
• 42234-86-6 diethyl heptadecanedioate 

Relevant academic research and scientific papers

LIPIDS FROM THE BROWN ALGA CYSTOSEIRA BARBATA

Two new diunsaturated lipids, related to palmitic acid, were isolated from the brown alga Cystoseira barbata, one of which is toxic to mice during P388 lymphocytic leukemia tests. Key Word Index - Cystoseira barbata; Phaeophyceae; brown alga, ethyl-(Z),(Z)-hexadec-10,13-dienate; (Z),(Z)-hexadec-10,13-dienal.

Photoaffinity probes for nematode pheromone receptor identification

Identification of pheromone receptors plays a central role for uncovering signaling pathways that underlie chemical communication in animals. Here, we describe the synthesis and bioactivity of photoaffinity probes for the ascaroside ascrNo.8, a sex-pheromone of the model nematode, Caenorhabditis elegans. Structure-activity studies guided incorporation of alkyne- and diazirine-moieties and revealed that addition of functionality in the sidechain of ascrNo.8 was well tolerated, whereas modifications to the ascarylose moiety resulted in loss of biological activity. Our study will guide future probe design and provides a basis for pheromone receptor identification via photoaffinity labeling in C. elegans.

Silica-Mediated Monohydrolysis of Dicarboxylic Esters

A new method for the monohydrolysis of dicarboxylic esters is presented, involving as key step a silanolysis at elevated temperatures at the silica gel surface. In the second step, the surface bound silyl esters are cleaved off under mild conditions, giving a straightforward and fast access to half esters. Based on recovered starting material generally yields well above 70 % are achieved, both, with stiff aromatic as well as flexible aliphatic substrates, as long as the ester groups involved are remote enough from each other. Otherwise competing reactions are becoming determinative, anhydride formation in the case of phthalates and decarbonylative fragmentation in the case of malonates. The new method was also successfully tested on a multigram scale with a minimalistic apparatus setup.

Synthetic method of acid compound

The invention belongs to the field of organic synthesis, and particularly relates to a synthetic method of an acid compound. An acid anhydride compound and an alkyl bromide or a functionalized alkyl bromide are subjected to a cross-electrophilic coupling reaction to synthesize an acid compound, so that the application of the alkyl bromide in the cross-electrophilic coupling reaction is expanded, and a novel non-traditional method for chemically and selectively constructing a carbon-carbon bond through a decarburization process is provided. The synthesis method is simple, economic, green and environment-friendly, and has wider applicability or is suitable for large-scale production.

CATIONIC LIPID

The present invention provides a cationic lipid which can be utilized for nucleic acid delivery into the cytoplasm. The cationic lipid of the present invention is, for example, a compound represented by the following Formula (1) or a pharmaceutically acceptable salt thereof.

Synthesis of fluorescent carboxylic acid ligands for construction of monolayers on nanostructures

Two new long-chain carboxylic acids (1, 2) bearing strong fluorescent group pyrene as ligands for Self-Assembled Monolayers (SAMs) have been synthesized. The multistep targeted synthesis is accomplished by use of Pyren-1-yl methylamine hydrochloride and employing simplified synthetic protocols. Compound 2 contains a chiral center purposely introduced along the atom chain in order to make it suitable for chiro-optical studies of the resulting SAMs.

Influence of positional isomers on the macroscale and nanoscale architectures of aggregates of racemic hydroxyoctadecanoic acids in their molecular gel, dispersion, and solid states

Inter/intramolecular hydrogen bonding of a series of hydroxystearic acids (HSAs) are investigated. Self-assembly of molecular gels obtained from these fatty acids with isomeric hydroxyl groups is influenced by the position of the secondary hydroxyl group. 2-Hydroxystearic acid (2HSA) does not form a molecular dimer, as indicated by FT-IR, and growth along the secondary axis is inhibited because the secondary hydroxyl group is unable to form intermolecular H-bonds. As well, the XRD long spacing is shorter than the dimer length of hydroxystearic acid. 3-Hydroxystearic acid (3HSA) forms an acyclic dimer, and the hydroxyl groups are unable to hydrogen bond, preventing the crystal structure from growing along the secondary axis. Finally, isomers 6HSA, 8HSA, 10HSA, 12HSA, and 14HSA have similar XRD and FT-IR patterns, suggesting that these molecules all self-assemble in a similar fashion. The monomers form a carboxylic cyclic dimer, and the secondary hydroxyl group promotes growth along the secondary axis.

Synthesis and anti-cancer activity of C-ring-functionalized prodigiosin analogues

Prodigiosin is the parent member of the 4-methoxypyrrolyldipyrromethene family of natural products and is known for its anti-cancer activity. A new series of analogues was synthesized, incorporating pendent functional esters and β-carbonyl substituents on the C-ring. The β-carbonyl group allowed for the facile isolation of the prodigiosenes, and the pendent esters allow for further derivatization. The novel prodigiosenes generally retain the anti-cancer activity of prodigiosin in 60 human cell lines derived from nine cancer cell types, with neither the conjugated /3-carbonyl group, as either ketone or ester, nor the pendent ester significantly reducing the anti-cancer activity of the core skeleton.

Process for producing ferrocenoyl derivatives

Disclosed is a process for producing a ferrocenoyl derivative comprising the reaction of ferrocene derivative with monocarboxylic acid or dicarboxylic acid in the presence of a catalyst. The ferrocenoyl derivative obtained by said process is very useful as the intermediate product for various functional materials, among all, for the micelle forming agents (surfactants) in so-called Micellar Disruption Method or the intermediate product of it.