Description

Indoxacarb Impurity 3 CAS NO 133001-07-7 is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for ensuring the quality, safety, and regulatory compliance of the active pharmaceutical ingredient (API) Indoxacarb. It is primarily required by analytical laboratories, quality control (QC) departments, and research institutions involved in pesticide development and pharmaceutical impurity profiling. The material is essential for method development, validation, and routine batch analysis.

Application

• Pharmaceutical Impurity Profiling and Identification in the analysis of Indoxacarb API.
• Analytical Method Development and Validation for HPLC, GC, or LC-MS systems.
• Quality Control and Assurance (QC/QA) as a certified reference material for batch release testing.
• Regulatory Compliance and Documentation to meet standards set by agencies like the EPA, FDA, and EMA.
• Stability Studies to monitor the formation of degradation products over time.
• Research and Development (R&D) in agrochemical and pharmaceutical synthesis pathways.
• Calibration of Analytical Instruments to ensure accurate and precise measurements.
• Teaching and Academic Research in chemistry and analytical science programs.

Basic Information

Item	Detail
Product Name	Indoxacarb Impurity 3
CAS No.	133001-07-7
Molecular Formula	C22H17ClF3N3O7
Molecular Weight	527.83 g/mol
Synonyms	7-Chloro-2,5-dihydro-2-[[(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]amino]carbonyl]indeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylic Acid Methyl Ester; Methyl 7-chloro-2,5-dihydro-2-({[(4-trifluoromethoxyphenyl)amino]carbonyl}carbamoyl)indeno[1,2-e][1,3,4]oxadiazine-4a-carboxylate; Indoxacarb Related Compound; Indoxacarb Metabolite Standard; DPX-JW062 Impurity; Oxadiazine Impurity.
EINECS	Contact for details

Quality Control

Every batch of Indoxacarb Impurity 3 is manufactured and tested under strict quality management systems. Our products undergo rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing all test results against established specifications. We adhere to relevant industry guidelines to support our clients' regulatory submissions.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single unknown impurity ≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 1.0% w/w
Heavy Metals	≤ 20 ppm

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