69679-30-7

Basic information

• Product Name: DecylParaben(decyl4-hydroxybenzoate)
• Synonyms: DecylParaben(decyl4-hydroxybenzoate);Decyl 4-hydroxybenzoate
• CAS NO: 69679-30-7
• Molecular Formula: C₁₇H₂₆O₃
• Molecular Weight: 278.38654
• EINECS: -0
• Mol File: 69679-30-7.mol
• Article Data: 11

Chemical Properties

• Melting Point: 58°C
• Boiling Point: 381.2°C (rough estimate)
• Flash Point: 156.3°C
• Appearance: /
• Density: 1.0352 (rough estimate)
• Vapor Pressure: 7.48E-07mmHg at 25°C
• Refractive Index: 1.5490 (estimate)
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: 24.5mg/L(25 oC)
• CAS DataBase Reference: DecylParaben(decyl4-hydroxybenzoate)(CAS DataBase Reference)
• NIST Chemistry Reference: DecylParaben(decyl4-hydroxybenzoate)(69679-30-7)
• EPA Substance Registry System: DecylParaben(decyl4-hydroxybenzoate)(69679-30-7)

Safety Data

• Hazardous Substances Data: 69679-30-7(Hazardous Substances Data)

Usage

General Description

DecylParaben, also known as decyl 4-hydroxybenzoate, is a chemical compound commonly used in the production of a wide range of personal care and cosmetic products as a preservative. It is a member of the paraben family, which are esters of para-hydroxybenzoic acid. DecylParaben is effective in preventing the growth of bacteria, yeast, and mold in products, thus extending their shelf life. It is known for its antimicrobial properties and is considered safe for use in low concentrations in personal care products, although there is ongoing debate about its potential risks and health effects with long-term use. Overall, DecylParaben is widely used for its preservative properties in a variety of consumer products.

InChI:InChI=1/C17H26O3/c1-2-3-4-5-6-7-8-9-14-20-17(19)15-10-12-16(18)13-11-15/h10-13,18H,2-9,14H2,1H3

Upstream product

• 112-30-1 1-Decanol 
• 99-96-7 4-hydroxy-benzoic acid 
• 123-08-0 4-hydroxy-benzaldehyde 
• 89155-65-7 1-(tert-butyldimethylsilyl)oxydecane 

Downstream Products

• 1194090-83-9 C₈₁H₉₀O₁₈ 
• 110188-49-3 4-(2-ethoxypropyloxy)benzoic acid 4'(decyloxycarbonyl)phenyl ester 
• 135329-86-1 C₃₃H₄₆O₆ 
• 135329-86-1 C₃₃H₄₆O₆ 
• 135329-90-7 C₂₅H₃₀O₅ 

Relevant articles and documents

Novel Benzothiazole Ionic Liquids as Catalysts for the Synthesis of Parabens

Abstract: A simple and green approach to the esterification of p-hydroxybenzoic acid and aliphatic alcohols to obtain parabens was developed. First, two novel benzothiazole ionic liquids [HBth]H2PW12O40 (IL1) and [HBth]H4PMo12O41 (IL2) were synthesized with benzothiazole and heteropolyacids as starting materials. The synthesized ionic liquids were characterized by FTIR spectroscopy, TGA, PXRD analysis, and SEM. The application of IL1 and IL2 as catalysts for the synthesis of parabens was explored. The results showed that the ILs had a high catalytic activity in the synthesis of parabens, and, at the same time, they could be easily recovered and reused five times without loss of activity.

Zirconocene-catalyzed direct (trans)esterification of acyl acids (esters) and alcohols in a strict 1:1 ratio under solvent-free conditions

A highly efficient way for the direct (trans)esterification of acyl acids (esters) and alcohols in a strict 1:1 ratio using a zirconocene complex (1, 1 mol%), a strong Lewis acid of good water tolerance, as a catalyst under solvent-free conditions has been developed. A wide range of acid and alcohol (esters) substrates undergo (trans)esterification to produce carboxylic ester motifs in moderate to good or excellent yields with good functional tolerance, such as that towards C-Br as well as CC and CC bonds. And complex 1 can be recycled six times without showing a significant decline in catalytic efficiency. It was demonstrated that cyclandelate, which is used to treat high blood pressure as well as heart and blood-vessel diseases, can be directly synthesized on a gram scale with 81% yield (6.70 g) using complex 1.

Inhibition of estrone sulfatase (ES) by alkyl and cycloalkyl ester derivatives of 4-[(aminosulfonyl)oxy] benzoic acid

In our search for potent inhibitors of the enzyme estrone sulfatase (ES), we have undertaken the synthesis and biochemical evaluation of a range of esters of 4-[(aminosulfonyl)oxy] benzoic acid. The results of the study show that the synthesised compounds possess potent inhibitory activity, indeed the cyclooctyl derivative was found to be more potent than 667-COUMATE, which is currently undergoing clinical trials.