3625-52-3

Usage

Uses

Used in Cosmetics and Personal Care Industry:
Dotriacontanoic acid is used as an emollient and skin conditioning agent for its ability to soften and smooth the skin, providing a luxurious feel and improving the overall texture.
Used in Pharmaceutical Industry:
Dotriacontanoic acid is utilized as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Lubricant Industry:
Due to its long-chain structure and saturated nature, dotriacontanoic acid is used as a lubricant in various applications, such as in the manufacturing of high-performance greases and other lubricating products.
Used in Chemical Synthesis:
Dotriacontanoic acid serves as a valuable building block in the synthesis of other organic compounds, including surfactants, polymers, and specialty chemicals, due to its unique structural properties.

InChI:InChI=1/C32H64O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31-32(33)34/h2-31H2,1H3,(H,33,34)

Upstream product

• 120364-18-3 14-oxo-dotriacontanoic acid 
• 120364-35-4 10-oxo-dotriacontanoic acid 
• 71353-61-2 tritriacontan-1-ol 
• 145204-11-1 Triacontanyl dotriacontanoate 
• 78529-59-6 Methyl-10-oxo-dotriacontanoate 
• 14065-32-8 methyl 10-chloro-10-oxodecanoate 
• 818-88-2 sebacic acid mono methyl ester 
• 61847-93-6 tritriacont-1-yne 
• 122335-20-0 14-oxo-dotriacontanoic acid ethyl ester 
• 93813-44-6 octane-1,1,8-tricarboxylic acid triethyl ester 

Downstream Products

• 6624-79-9 dotriacontan-1-ol 

Relevant academic research and scientific papers

FLAVONOIDS AND OTHER CONSTITUENTS FROM PEDALIUM MUREX

Two new compounds isolated from the fruits of Pedalium murex were characterized as 2',4',5'-trihydroxy-5,7-dimethoxyflavone and triacontanyl dotriacontanoate by physico-chemical methods.Luteolin, rubusic acid, nonacosane, tritriacontane, triacontanoic acid, tritriacontanoic acid and sitosterol β-D-glucoside have also been isolated and identified. Key words: Pedalium murex; Pedaliaceae; fruits; 2',4',5'-trihydroxy-5,7-dimethoxyflavone; luteolin; rubusic acid; triacontanyl dotriacontanoate; lipids.

Organoboranes for synthesis. 13. Simple, efficient syntheses of long-chain alcohols and carboxylic acids

General, convenient and simple syntheses of long straight chain alcohols and carboxylic acids were developed utilizing organoborane chemistry. One of the methods entails the thermal isomerization of long-chain alkyldicyclohexylboranes, followed by oxidation. An alternative procedure for the preparation of long-chain alcohols involves the KAPA isomerization of internal alkynes to the terminal derivative, followed by dihydroboration with 9-BBN and oxidation. Alternatively, the terminal alkyne can be oxidised directly to the carboxylic acid. In another strategy, the C30-alcohol triaxontanol was prepared by employing high pressure carbonylation of a borane intermediate.

Effects of structural variations of non-ionic surfactants on micellar properties and solubilization: surfactants containing very long hydrocarbon chains

Polyoxyethylene mono-ethers of dotriacontanol (C32E41) and 4,9-dimethyltritriacontanol (C35E40) have been synthesized. The micellar weights in water at 298K were 4.82 x 105 and 5.90 x 105, the aggregation numbers 212 and 260, and the levels of hydration 290 and 283 mol water mol-1 surfactant, respectively. The solubilization of azobenzene, cortisone acetate, griseofulvin, sulphadiazine, phenylbutazone, betamethasone, tolbutamide, and menaphthone was studied in 2% solutions of the above surfactants. The presence of large micelles did not result in increased solubilization; C32E41 and C35E40 had a lower solubilizing capacity than that of cetomacrogol.

Lacceryl laccerate: Major Wax Component Produced by Anomoneura mori Schwarz (Homoptera: Psyllidae)

The major wax component secreted by Anomoneura mori Schwarz nymph was identified as laccerate, n-dotriacontyl n-dotriacontanoate.Its content in the wax 93.8percent.