26976-72-7

Basic information

• Product Name: Aceburic Acid
• Synonyms: Aceburic acid [INN:DCF]; Aceburic acid; UNII-F777XEP0LL; 4-Hydroxybutyric acid acetate; 4-(acetyloxy)butanoic acid
• CAS NO: 26976-72-7
• Molecular Formula: C₆H₁₀O₄
• Molecular Weight: 146.1412
• Mol File: 26976-72-7.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 272.1°C at 760 mmHg
• Flash Point: 113.4°C
• Density: 1.162g/cm³
• Vapor Pressure: 0.00173mmHg at 25°C
• Refractive Index: 1.44
• CAS DataBase Reference: Aceburic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: Aceburic Acid(26976-72-7)
• EPA Substance Registry System: Aceburic Acid(26976-72-7)

Safety Data

• Hazardous Substances Data: 26976-72-7(Hazardous Substances Data)

Usage

General Description

Aceburic acid, also known as 2,4-Dinitrophenylacetic acid, is a chemical compound that is derived from acetic acid. It is used as an intermediate in the production of pharmaceuticals and dyes. Aceburic acid is a yellow to orange crystalline powder that is insoluble in water but soluble in alcohol and ether. It is a known irritant to the skin, eyes, and respiratory system, and exposure to high concentrations can cause irritation and damage. Its primary use is in the synthesis of various pharmaceutical drugs and research chemicals. Aceburic acid is also used as a reagent in analytical chemistry for various tests including the detection and quantification of certain functional groups.

Upstream product

• 1670-46-8 2-acetylcyclopentanaone 
• 96-48-0 4-butanolide 
• 108-24-7 acetic anhydride 
• 59854-06-7 tert-butyl 4-(acetyloxyl)butanoate 
• 6564-95-0 4-oxobutyl acetate 
• 502-85-2 sodium 4-hydroxybutanoate 
• 75-36-5 acetyl chloride 
• 25560-93-4 benzyl 4-(acetyloxy)butanoate 
• 71568-66-6 2-Oxo-2-phenylaethyl-4-acetyloxy-butanoat 
• 591-81-1 4-hydroxybutanoic acid 

Downstream Products

• 1344702-49-3 C₅₅H₅₅N₁₃O₁₁S₆ 
• 52762-40-0 2-(4-Acetoxybutyryl)-cyclohexanon 
• 13045-16-4 5-Acetyloxy-1-chlor-pentan-2-on 

Relevant articles and documents

PANTETHEINE DERIVATIVES AND USES THEREOF

The present disclosure relates to compounds of Formula (I), (II), or (II'): (I), (II), (II'), and pharmaceutically acceptable salts or solvates thereof. The present disclosure also relates to pharmaceutical compositions comprising the compounds and therapeutic and diagnostic uses of the compounds and pharmaceutical compositions.

Thermal and photochemical oxidation of 2-acetylcyclopentanone with atmospheric oxygen

The major products of thermal (acetone, CaCl2 excess, reflux) and photochemical (acetone or CCl4, room temperature) oxidation of 2-acetylcyclopentanone with atmospheric oxygen are 2-acetyl-2- hydroxycyclopentanone, 2-acetyl-2-hydroxy

NOVEL NITROSO COMPOUNDS AS NITROXYL DONORS AND METHODS OF USE THEREOF

The invention relates to nitroso derivatives including carboxylic acid and phosphoric acid esters of hydroxy nitroso compounds that donate nitroxyl (HNO) under physiological conditions. The compounds and compositions of the invention are useful in treating and/or preventing the onset and/or development of diseases or conditions that are responsive to nitroxyl therapy, including heart failure, ischemia/reperfusion injury and cancer.