Description

1-n-(2-Hydroxyethyl)Acetamido-2-Hydroxylaminoimidazole-Glutathione Conjugate is a specialized biochemical conjugate that combines a modified imidazole derivative with the endogenous antioxidant glutathione. This compound matters for researchers and formulators seeking to study or modulate oxidative stress pathways and cellular defense mechanisms. It is primarily needed by the pharmaceutical, biotechnology, and advanced life science research sectors for applications in drug discovery, biochemical research, and the development of novel therapeutic agents.

Application

• Biochemical Research: Used as a reference standard or probe in studies investigating glutathione conjugation pathways, oxidative stress, and cellular redox biology.
• Pharmaceutical Development: Serves as a key intermediate or model compound in the research and development of new drugs targeting oxidative damage or enhancing cellular antioxidant capacity.
• Metabolite Studies: Employed in the identification and quantification of related metabolites in pharmacokinetic and metabolic profiling studies.
• Enzymology: Acts as a substrate or inhibitor in assays for enzymes involved in glutathione metabolism, such as glutathione S-transferases (GSTs).
• Nutraceutical & Cosmeceutical Research: Investigated for potential applications in formulations aimed at combating oxidative stress at the cellular level for health and cosmetic benefits.

Basic Information

Product Name	1-n-(2-Hydroxyethyl)Acetamido-2-Hydroxylaminoimidazole-Glutathione Conjugate
CAS No.	104939-14-2
Molecular Formula	C17H28N6O8S
Molecular Weight	476.50 g/mol
Synonyms	1-(2-Hydroxyethyl)-N-acetamido-2-hydroxylaminoimidazole-Glutathione Conjugate; GSH Conjugate of 1-N-Acetoxy-2-(2-hydroxyethylamino)imidazole; Glutathione S-Conjugate; 1-N-Acetamido-2-(2-hydroxyethylamino)imidazole Glutathionyl Adduct; HAIG-GSH Conjugate; (2S)-2-Amino-4-[[(2R)-1-[[(2R)-2-[[2-[[2-(2-Hydroxyethylamino)-2-imidazolyl]amino]-2-oxoethyl]amino]-1-(carboxymethylamino)-1-oxo-3-sulfanylpropyl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-4-oxobutanoic Acid (IUPAC); 104939-14-2; Acetamido Hydroxylamino Imidazole Glutathione Adduct
EINECS	Contact for details

Quality Control

Our 1-n-(2-Hydroxyethyl)Acetamido-2-Hydroxylaminoimidazole-Glutathione Conjugate is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the high standards required for research and development. Certificates of Analysis (COA) detailing batch-specific results are available upon request to support your quality assurance and regulatory documentation needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed in a desiccated environment and away from direct light exposure to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 5.0%
Heavy Metals	≤ 20 ppm
Residual Solvents (GC)	Meets ICH guidelines

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.