26215-92-9

Usage

Uses

Used in Chemical Production:
4-Tridecanol is used as an intermediate in the production of various chemical products, including surfactants, lubricants, and plasticizers. Its long-chain structure and solubility in organic solvents make it a valuable component in these formulations.
Used in Cosmetics Industry:
In the cosmetics industry, 4-Tridecanol is used as an additive for its emollient properties, helping to improve the texture and feel of cosmetic products. Its compatibility with organic solvents aids in the formulation of various cosmetic products.
Used in Flavoring Agents:
4-Tridecanol is utilized as a component in flavoring agents, where its chemical structure contributes to the development of specific tastes and scents in food and beverage products.
Used in Industrial Chemicals:
4-Tridecanol is also used in the production of industrial chemicals, where its properties can be leveraged to enhance the performance of various chemical formulations.
Used in Synthesis of Other Chemicals:
4-Tridecanol serves as a raw material for the synthesis of other chemicals such as esters and carboxylic acids, expanding its utility in the chemical industry.
It is crucial to handle 4-Tridecanol with care due to its potential to cause irritation to the eyes, skin, and respiratory system, and its classification as a hazardous substance.

InChI:InChI=1/C13H28O/c1-3-5-6-7-8-9-10-12-13(14)11-4-2/h13-14H,3-12H2,1-2H3

Upstream product

• 26215-90-7 tridecan-4-one 
• 39691-62-8 nonylmagnesium bromide 
• 123-72-8 butyraldehyde 
• 111-87-5 octanol 
• 6032-29-7 (+/-)-2-pentanol 

Downstream Products

• 26215-90-7 tridecan-4-one 
• 30714-90-0 C₁₃H₂₇O₅S^(1-)*Na⁽¹⁺⁾ 

Relevant academic research and scientific papers

Ruthenium-catalyzed β-alkylation of secondary alcohols with primary alcohols

The catalytic properties of a series of ruthenium complexes for β-alkylation of secondary alcohols with primary alcohols were studied. The catalytic activities of the ruthenium complexes were found to be dependent on the auxiliary ligands. The most active catalytic precursor found in this study is the ruthenium complex RuCl2(PPh3)2(2-NH2CH2Py) [2-NH2CH2Py = 2-aminomethyl pyridine], which effectively catalyzed the β-alkylation of both aryl- and alkyl-substituted secondary alcohols with benzylic and alkyl primary alcohols.

Small molecule probes of the receptor binding site in the Vibrio cholerae CAI-1 quorum sensing circuit

Based on modification of separate structural features of the Vibrio cholerae quorum sensing signal, (S)-3-hydroxytridecan-4-one (CAI-1), three focused compound libraries have been synthesized and evaluated for biological activity. Modifications to the acyl tail and α-hydroxy ketone typically provided agonists with activities correlated to tail length and conservative changes to the hydroxy ketone. Among the molecules identified within this collection of agonists is Am-CAI-1 (B11), which is among the most potent agonists reported to date with an EC50 of 0.21 μM. Modifications to the ethyl side chain delivered molecules with both agonist and antagonist activity, including m-OH-Ph-CAI-1 (C13) which is the most potent antagonist reported to date with an IC50 of 36 μM. The molecules described in this manuscript are anticipated to serve as valuable tools in the study of quorum sensing in Vibrio cholerae and provide new leads in the development of an antivirulence therapy against this human pathogen.