Description

6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane Boceprevir Key Intermediate is a high-purity, advanced pharmaceutical intermediate critical for the synthesis of Boceprevir, a protease inhibitor used in antiviral therapies. This compound is essential for manufacturers requiring a reliable and consistent building block to ensure the efficacy and purity of the final active pharmaceutical ingredient (API). It is primarily targeted at pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and API producers engaged in the development and production of antiviral medications.

Application

• Primary Intermediate for the synthesis of Boceprevir (Victrelis®), an antiviral medication.
• Key Building Block in pharmaceutical research and development for hepatitis C virus (HCV) protease inhibitors.
• Critical Raw Material for Contract Manufacturing Organizations (CMOs) producing antiviral APIs under cGMP.
• Reference Standard for analytical method development and quality control in pharmaceutical manufacturing.
• Process Chemistry for scaling up and optimizing synthetic routes to Boceprevir and related compounds.

Basic Information

Product Name	6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane Boceprevir Key Intermediate
CAS No.	943516-54-9
Molecular Formula	C9H15N
Molecular Weight	137.22 g/mol
Synonyms	6,6-Dimethyl-3-azabicyclo[3.1.0]hexane; (1R,5S)-6,6-Dimethyl-3-azabicyclo[3.1.0]hexane; Boceprevir Intermediate; Bicyclo[3.1.0]hexane, 6,6-dimethyl-3-aza-; 3-Azabicyclo[3.1.0]hexane, 6,6-dimethyl-; Boceprevir Key Building Block; CAS 943516-54-9
EINECS	Contact for details

Quality Control

Our 6,6-Dimethyl-3-Azabicyclo[3.1.0]Hexane Boceprevir Key Intermediate is manufactured under strict quality systems suitable for pharmaceutical applications. We provide comprehensive quality documentation, including a Certificate of Analysis (COA) for each batch, detailing purity, identity, and impurity profiles. Our quality commitment ensures the material meets the stringent standards required for cGMP manufacturing and advanced pharmaceutical synthesis.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive); keep the container tightly sealed in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Assay (HPLC)	≥98.0%
Purity (HPLC, Area %)	≥99.0%
Water Content (KF)	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤10 ppm

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