share

Clazolam CAS NO 7492-29-7


Unit Price:

CAS No.:7492-29-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Clazolam is a high-purity benzodiazepine derivative, recognized for its specific pharmacological research applications. This compound is of significant interest for advanced pharmaceutical development and analytical reference purposes. It serves as a critical intermediate and reference standard for researchers and developers in the pharmaceutical, biotechnology, and forensic science sectors.

Application

  • Pharmaceutical Research & Development: Used as a key intermediate in the synthesis of novel therapeutic agents and for studying structure-activity relationships (SAR).
  • Reference Standard: Serves as a certified analytical standard for quality control (QC) and method validation in laboratory testing.
  • Biochemical Studies: Employed in pharmacological and neurochemical research to investigate receptor binding and metabolic pathways.
  • Forensic Analysis: Utilized as a calibration standard in forensic toxicology for the identification and quantification of related compounds.
  • Academic Research: Applied in university and institutional labs for chemical education and advanced scientific studies.

Basic Information

Product Name Clazolam
CAS No. 7492-29-7
Molecular Formula C17H12Cl2N2O
Molecular Weight 331.20 g/mol
Synonyms 7-Chloro-5-(2-chlorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one; 7-Chloro-5-(o-chlorophenyl)-1,3-dihydro-1-methyl-2H-1,4-benzodiazepin-2-one; Clazolamum; Sch-15719; Wy-15719; Clazolam (USAN); 1-Methyl-7-chloro-5-(2-chlorophenyl)-1,3-dihydro-2H-1,4-benzodiazepin-2-one
EINECS Contact for details

Quality Control

Our Clazolam is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including HPLC, NMR, and mass spectrometry, to confirm identity and potency. A detailed Certificate of Analysis (COA) is provided with every shipment, documenting all critical quality attributes. We adhere to cGMP principles for pharmaceutical intermediates to support our clients' regulatory requirements.

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 (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying ≤ 1.0%
Residue on Ignition ≤ 0.1%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.