4432-64-8

Usage

Uses

Used in Cosmetic Industry:
1-(2-AMINOETHYL)-2-IMIDAZOLIDONE is used as a cosmetic preservative for its broad-spectrum antimicrobial and anti-fungal properties, providing an effective alternative to traditional preservatives without the associated health concerns.
Used in Haircare Products:
1-(2-AMINOETHYL)-2-IMIDAZOLIDONE is used as a conditioning agent in haircare products, helping to improve the texture and manageability of hair while providing protection against damage.
Used in Skincare Products:
1-(2-AMINOETHYL)-2-IMIDAZOLIDONE is used as an emollient in skincare products, contributing to the softness and smoothness of the skin by reducing moisture loss and providing a protective barrier.
Used as a Viscosity Control Agent:
1-(2-AMINOETHYL)-2-IMIDAZOLIDONE is used to control the viscosity of cosmetic formulations, ensuring a consistent texture and improving the overall performance of the product.

Upstream product

• 50704-41-1 2-diazo-malonaldehyde 
• 71-43-2 benzene 
• 106636-96-8 5-phenyl-1,2,3-triazine 
• 103-82-2 phenylacetic acid 
• 36838-59-2 N-styrylmorpholine 

Downstream Products

• 86139-82-4 methoxy-3 phenyl-2 propenal 
• 856063-95-1 1-(2-nitro-phenyl)-4-phenyl-1H-pyrazole 
• 105688-72-0 3-anilino-2-phenyl-acrylaldehyde 
• 15132-01-1 1,4-diphenyl-1H-pyrazole 
• 56863-46-8 1-methyl-5-phenyl-2(1H)-pyrimidinone 
• 10199-68-5 4-phenyl-1H-pyrazole 
• 2439-92-1 4-phenylisoxazole 
• 21555-03-3 phenylmalonaldehyde monooxime 
• 67002-91-9 1,5-bis-(6-ethyl-2-phenyl-thiazolo[5',4':3,4]benzo[1,2-d]oxazol-7-yl)-3-phenyl-pentamethinium; iodide 
• 63339-78-6 1,5-bis-(5-benzooxazol-2-yl-3-ethyl-1-phenyl-benzoimidazol-2-yl)-3-phenyl-pentamethinium; iodide 
• 63339-79-7 1,5-bis-(5-benzothiazol-2-yl-3-ethyl-1-phenyl-benzoimidazol-2-yl)-3-phenyl-pentamethinium; iodide 
• 1026365-83-2 (1-Methoxycarbonylmethylsulfanyl-3-oxo-2-phenyl-propylsulfanyl)-acetic acid methyl ester 
• 81267-50-7 5,7-dihydroxyisoflavylium chloride 
• 2458-26-6 3-phenylpyrazole 

Relevant academic research and scientific papers

Probing the Scope of the Amidine–1,2,3-triazine Cycloaddition as a Prospective Click Ligation Method

Despite recent achievements in the development of chemical reactions enabling selective modification of complex biomolecules, the demand for fast and efficient methodologies that allow the attachment of various functional groups to these systems is the subject of intense research. Here, we report on the study of the amidine–1,2,3-triazine cycloaddition reaction, which has the potential to address many of the challenges associated with the development of such chemistry. We describe an optimized protocol leading to the in situ formation of free amidine bases, which directly react in the cycloaddition reaction with 1,2,3-triazines. Our kinetic studies reveal the structural features determining the reaction rates. Finally, we show that the amidine–1,2,3-triazine cycloaddition is extraordinarily selective and orthogonal to other popular ligation reactions. The pros and cons of the methodology are presented.

Design, synthesis, and antifungal activity of inhibitors of brassilexin detoxification in the plant pathogenic fungus Leptosphaeria maculans

Potential inhibitors of Leptosphaeria maculans mediated detoxification of the phytoalexin brassilexin were designed and synthesized based on the planar heteroaromatic structure of isothiazolo[5,4-b]indole. Screening of these compounds for inhibition of br

A Synthesis of Hydroxylated Isoflavylium Salts and Their Reduction Products

Phloroglucinol reacts with arylmalondialdehydes in the presence of hydrochloric acid to form 5,7-dihydroxyisoflavylium salts.Reduction of these salts can be utilized to form isoflav-2-enes, isoflav-3-enes or isoflavans.