2-(Hexamethyleneimino)ethyl chloride Hydrochloride CAS: 26487-67-2

Product Parameters
Catalog No. BK707R
CAS.RN 26487-67-2
Molecular Formula C8H17Cl2N
Molecular Weight 198.13 g/mol
Purity NLT 98%
Product Overview

2-(cyclohexylimino)ethyl chloride, as a pharmaceutical intermediate, is mainly used in the synthesis of nitrogen-containing heterocyclic compounds and active pharmaceutical ingredients, and is widely used in the research and development and production of innovative drugs such as anti-tumor and antibacterial drugs. This product is suitable for preliminary exploration, small-scale preparation, pilot-scale amplification, and commercial production in the research and development stage. It possesses good chemical stability and reactivity, and can provide customers with high-quality, high-purity raw material support, helping them accelerate process development and project transformation.

Applications
  • Synthesis of nitrogen-containing heterocyclic drug intermediates
  • Synthesis of key intermediates for antitumor drugs
  • Molecular structure modification of antibacterial drugs
  • Introduction of functional groups in pharmaceutical R&D
  • Process route optimization and customized synthesis
Quality & Supply Capability

English Name: 2-(Hexamethyleneimino)ethyl chloride Hydrochloride Properties: This product is a white to off-white crystalline powder with a stable cyclohexylimino structure and chloroethyl functional groups. It is readily soluble in polar organic solvents, exhibits good chemical stability, and is suitable for various organic synthesis reaction systems. Storage Recommendations: Store in a sealed, light-protected, and dry place, referring to the COA/MSDS for specific details. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust purity standards, impurity control requirements, packaging specifications, and delivery cycles according to customer needs, and provide complete quality documentation support. Furthermore, we have a professional technical team that can provide customers with comprehensive technical support from the initial R&D stage to industrial production, assisting customers in process development, route optimization, and project transformation to ensure efficient and compliant project progress.

Why Choose Bioncan

Focused on the pharmaceutical intermediates field, with years of experience and extensive expertise in product development and supply. Full-scale supply capabilities to meet diverse needs from laboratory to commercial production. Comprehensive quality control documentation, including COA, MSDS, HPLC, NMR, etc., ensuring controllable product quality. Customization support available, flexibly tailored to customer requirements regarding purity, impurities, packaging, and delivery time. Support for process optimization and scale-up technologies to facilitate a smooth transition from R&D to production.

Products are offered for research, development, or industrial use only.
Customers are responsible for ensuring compliance with applicable patent, regulatory, and import/export requirements in their respective jurisdictions.
Online Consulting

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