53488-15-6

Basic information

• Product Name: [(2-ethylhexyl)oxy]acetaldehyde
• Synonyms: [(2-ethylhexyl)oxy]acetaldehyde;Einecs 258-583-4
• CAS NO: 53488-15-6
• Molecular Formula: C₁₅H₁₇N₃
• Molecular Weight: 172.2646
• EINECS: 258-583-4
• Mol File: 53488-15-6.mol

Chemical Properties

• Boiling Point: 212.8°Cat760mmHg
• Flash Point: 64.3°C
• Appearance: /
• Density: 0.871g/cm³
• Vapor Pressure: 0.17mmHg at 25°C
• Refractive Index: 1.422
• CAS DataBase Reference: [(2-ethylhexyl)oxy]acetaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: [(2-ethylhexyl)oxy]acetaldehyde(53488-15-6)
• EPA Substance Registry System: [(2-ethylhexyl)oxy]acetaldehyde(53488-15-6)

Safety Data

• Hazardous Substances Data: 53488-15-6(Hazardous Substances Data)

Usage

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.

InChI:InChI=1/C10H20O2/c1-3-5-6-10(4-2)9-12-8-7-11/h7,10H,3-6,8-9H2,1-2H3

Upstream product

• 137-97-3 N,N'-di(o-tolyl)thiourea 
• 22695-18-7 N,N-di-o-tolylthiourea 
• 95-53-4 o-toluidine 
• 506-77-4 cyanogen chloride 
• 7664-41-7 ammonia 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 56-23-5 tetrachloromethane 
• 615-37-2 ortho-methylphenyl iodide 
• 124-46-9 guanidine hydrogen carbonate 
• 506-93-4 guanidine nitrate 
• 646-34-4 guanidinium sulfate 
• 95-46-5 2-methylphenyl bromide 
• 614-78-8 o-tolylthiourea 

Relevant articles and documents

Synthesis of symmetrical and unsymmetrical N, N ′-diaryl guanidines via copper/N-methylglycine-catalyzed arylation of guanidine nitrate

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.

Copper-catalyzed guanidinylation of aryl iodides: The formation of N,N′-disubstituted guanidines

Chemical Equation Presented A copper-catalyzed cross-coupling reaction of guanidine nitrate with aryl iodides was used for the formation of N,N′-disubstituted guanidines to be used as potential therapeutics for strokes. A relatively inexpensive commercially available guanidine salt and a series of aryl iodides together with copper iodide and N,N-diethylsalicylamide as an efficient catalyst/1 igand system provided a simple diarylation procedure.

Role of quaternaryammonium permanganates in the synthesis of substituted guanidines - A comparative study

Quaternaryammonium permanganate transforms 1,3-diarylthioureas in the presence of an amine to the respective trisubstituted guanidines in excellent yields.

A Short and Concise Synthesis of Guanidines

A facile high yielding process of guanidines is reported by reaction of amine nucleophiles on the oxidised thioureas in an aqueous medium using the unexploited reagents sodium chlorite and sodium metaperiodate for the oxidation of 1,3-disubstituted thioureas.

Disturbance-of-consciousness improving agent

The present invention provides a disturbance-of-consciousness improving agent which is a highly effective and quick remedy and which can be administered orally. The disturbance-of-consciousness improving agent of the invention contains a sigma receptor agonist compound as an active ingredient.

Lac sulfur on alumina-triethanolamine - An effective reagent for the synthesis of substituted guanidines

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.