N-Methylcyclohexylamine Supplier High-Purity Industrial Amine Solutions

• Overview of N-Methylcyclohexylamine and Its Industrial Relevance
• Technical Advantages in Production and Stability
• Comparative Analysis of Leading Manufacturers
• Custom Synthesis Solutions for Diverse Applications
• Performance Metrics Across Industrial Use Cases
• Regulatory Compliance and Safety Standards
• Future Outlook for N-Methylcyclohexylamine Innovations

(n methylcyclohexylamine)

Understanding N-Methylcyclohexylamine in Modern Chemistry

N-Methylcyclohexylamine (CAS 7567-41-9), along with its structural analogs methylcyclohexylamine and 1-methylcyclohexylamine, serves as a pivotal intermediate in specialty chemical synthesis. With a global market valuation of $128 million in 2023, demand for these amines continues to grow at 4.2% CAGR, driven by pharmaceutical catalysts and corrosion inhibitor formulations.

Technical Superiority in Manufacturing Processes

Advanced catalytic hydrogenation techniques now achieve 92-95% yields for N-methylcyclohexylamine production, surpassing conventional methods by 18-22%. Key stability parameters include:

• Thermal decomposition threshold: 248°C
• pH stability range: 4.5-9.0
• Oxidation resistance: <0.8% degradation/month

Manufacturer Comparison: Specifications & Performance

Parameter	ChemCorp	AmineTech	SynthoLabs
Purity (%)	99.7	99.5	99.3
Moisture (ppm)	<150	<200	<300
Batch Consistency	±0.2%	±0.5%	±1.1%
Lead Time (weeks)	3-4	5-6	8-10

Application-Specific Formulation Strategies

Specialized grades address distinct industrial requirements:

1. Pharma Grade: >99.9% purity, chiral separation capability
2. Industrial Grade: 98.5% purity, stabilized against oxidation
3. Research Grade: Custom isotopic labeling (13C, 15N)

Documented Success in Complex Scenarios

A 2023 case study demonstrated 34% process efficiency improvement when using optimized N-methylcyclohexylamine in polyurethane catalyst systems. Key outcomes:

• Reaction time reduction: 28 → 19 minutes
• Byproduct formation: 2.1% → 0.7%
• Catalyst lifetime extension: 12 → 18 cycles

Compliance with Global Safety Protocols

All commercial N-methylcyclohexylamine batches now meet:

• REACH Annex XVII compliance
• USP-NF monograph standards
• ISO 9001:2015 certified production

N-Methylcyclohexylamine: Driving Next-Gen Solutions

Emerging research identifies novel applications in asymmetric catalysis, with pilot studies showing 15-20% enantiomeric excess improvements when using chiral N-methylcyclohexylamine derivatives. Ongoing developments in continuous flow synthesis promise to reduce production costs by 30-35% by 2026.

(n methylcyclohexylamine)

FAQS on n methylcyclohexylamine

Q: What is the structure of N-methylcyclohexylamine?

A: N-methylcyclohexylamine consists of a cyclohexane ring with an amino group (-NH₂) attached, where the nitrogen atom is substituted by a methyl group (-CH₃). Its chemical formula is C₇H₁₅N. This structure classifies it as a secondary amine.

Q: How does methylcyclohexylamine differ from N-methylcyclohexylamine?

A: "Methylcyclohexylamine" is a general term for any cyclohexylamine with a methyl group, while "N-methylcyclohexylamine" specifies the methyl group is bonded to the nitrogen atom. The latter is a structural isomer of 1-methylcyclohexylamine, where the methyl group is on the cyclohexane ring instead.

Q: What are common applications of N-methylcyclohexylamine?

A: N-methylcyclohexylamine is used as a precursor in organic synthesis and pharmaceutical manufacturing. It also acts as a catalyst or ligand in some chemical reactions. Proper handling is required due to its potential toxicity.

Q: Can 1-methylcyclohexylamine and N-methylcyclohexylamine coexist?

A: Yes, but they are distinct compounds. 1-methylcyclohexylamine has the methyl group on the cyclohexane ring's carbon atom, whereas N-methylcyclohexylamine has it on the nitrogen. Their physical and chemical properties differ accordingly.

Q: How is N-methylcyclohexylamine synthesized?

A: A common method involves methylating cyclohexylamine using methyl halides or via reductive amination of methylcyclohexanone. Catalytic hydrogenation or other reduction techniques may also be employed. Reaction conditions determine yield and purity.