53488-15-6 Usage
Description
[(2-ethylhexyl)oxy]acetaldehyde, also known as O-Ethylhexylglycidal, is a chemical compound that serves as a preservative and fragrance ingredient in the personal care and cosmetic industry. It is a clear, colorless liquid with a sweet, fruity odor and is often used as an alternative to traditional preservatives like parabens. [(2-ethylhexyl)oxy]acetaldehyde is recognized for its antimicrobial and antifungal properties, which help extend the shelf life of products and prevent the growth of harmful microorganisms. However, it has also been linked to potential irritant and sensitizing effects on the skin, raising some safety concerns in specific applications. Nonetheless, [(2-ethylhexyl)oxy]acetaldehyde remains a widely used ingredient in a variety of consumer products.
Uses
Used in Personal Care and Cosmetic Products:
[(2-ethylhexyl)oxy]acetaldehyde is used as a preservative and fragrance ingredient for its antimicrobial and antifungal properties, which help extend the shelf life of products and prevent the growth of harmful microorganisms.
Used in the Fragrance Industry:
In the fragrance industry, [(2-ethylhexyl)oxy]acetaldehyde is used as a fragrance ingredient due to its sweet, fruity odor, enhancing the scent profiles of various products.
Used in the Preservation of Consumer Products:
As a preservative, [(2-ethylhexyl)oxy]acetaldehyde is used to maintain the quality and safety of products by inhibiting the growth of microorganisms, thus preventing spoilage and contamination.
Check Digit Verification of cas no
The CAS Registry Mumber 53488-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,8 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53488-15:
(7*5)+(6*3)+(5*4)+(4*8)+(3*8)+(2*1)+(1*5)=136
136 % 10 = 6
So 53488-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H20O2/c1-3-5-6-10(4-2)9-12-8-7-11/h7,10H,3-6,8-9H2,1-2H3
53488-15-6Relevant articles and documents
Synthesis of symmetrical and unsymmetrical N, N ′-diaryl guanidines via copper/N-methylglycine-catalyzed arylation of guanidine nitrate
Xing, Hui,Zhang, Ye,Lai, Yisheng,Jiang, Yongwen,Ma, Dawei
experimental part, p. 5449 - 5453 (2012/08/07)
CuI/N-methylglycine-catalyzed coupling reaction of guanidine nitrate with both aryl iodides and bromides takes place at 70-100 °C, affording symmetrical N,N′-diaryl guanidines with good to excellent yields. Unsymmetrical N,N′-diaryl guanidines can be assembled via monoarylation of guanidine nitrate with aryl iodides bearing a strong electron-withdrawing group and subsequent coupling with another aryl iodide.
Role of quaternaryammonium permanganates in the synthesis of substituted guanidines - A comparative study
Srinivasan, Natarajan,Ramadas, Krishnamurthy
, p. 343 - 346 (2007/10/03)
Quaternaryammonium permanganate transforms 1,3-diarylthioureas in the presence of an amine to the respective trisubstituted guanidines in excellent yields.
Lac sulfur on alumina-triethanolamine - An effective reagent for the synthesis of substituted guanidines
Ramadas, Krishnamurthy
, p. 5161 - 5162 (2007/10/03)
A direct synthesis of substituted guanidines is reported from their thiourea analogues. The strategy adopted is a concise approach to the synthesis of the title compounds.
