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High Purity 3,3-Dimethylpiperidine for Pharmaceutical Synthesis

Product Portal: 3,5-Dimethylpiperidine    |    CAS: 35794-11-7    |    EC No.: 252-637-5

As an essential intermediate in the fine chemicals and pharmaceuticals sector, 3,5-Dimethylpiperidine (also known as 3,5-DMP) plays a pivotal role in various high-value applications. With rapidly evolving industry trends and an increasing demand for high-purity, high-stability intermediates, market requirements for 3 and its derivatives have become stringent. This article provides an in-depth technical and market overview of 3, including latest process insights, properties, technical advantages, manufacturers’ strengths comparison, trend analysis, and real-life application successes.

1. Industry Trends and Market Prospects

According to the report by Grand View Research, the global demand for specialty amine derivatives such as 3,5-Dimethylpiperidine is exhibiting >6% CAGR. Its uses span catalysis, resin modifiers, fine chemical synthesis, active pharmaceutical ingredients (APIs), and even high-stability corrosion inhibitors for petrochemical pipelines.

  • The rising adoption of 3 as a core intermediate in pharmaceutical synthesis (notably antihistamines and antipsychotic agents).
  • Significantly increased utilization in corrosion protection, water treatment, and electronic chemical fields owing to its excellent chemical stability and structural selectivity.
  • Industry focus: Custom synthesis and high-purity refining, with enhanced trace impurity control and analytical rigor (GC/HPLC, ISO 9001:2015 and FDA process registration widely adopted).

Fig.1: 3,5-Dimethylpiperidine global market size, 2019–2024 (Source: Global Industry Analysis Reports)

2. Technical Parameters and Comparative Data

Parameter 3,5-Dimethylpiperidine (3,5-DMP) 2,6-Dimethylpiperidine Piperidine
Molecular Formula C7H15N C7H15N C5H11N
Molecular Weight 113.20 113.20 85.15
Boiling Point (°C) 156-157 157–158 106–108
Purity (GC) ≥ 99.0% ≥ 98.0% ≥ 97.5%
Water Content < 0.20% < 0.40% < 0.50%
Appearance Clear colorless liquid Clear liquid Colorless to pale yellow
Typical End Use APIs, specialty resins, corrosion inhibitors Pharma, catalysts, polymers Resins, solvents, pharma
Key Certifications ISO 9001, Reach, FDA Process ISO 9001, REACH ISO 9001

This comparative table underlines the technical superiority of 3, notably in terms of purity, water content, and advanced certifications, over similar piperidine derivatives.

Fig.2: Purity comparison among major Piperidine derivatives (Source: Third-party QC Reports, 2023)

3. Manufacturing Process Flow: 3,5-Dimethylpiperidine

The 3,5-Dimethylpiperidine manufacturing process adheres strictly to ISO 9001:2015 and REACH standards. Below is a streamlined process schematic demonstrating key steps:

1. Raw Materials Preparation

Selection of high-purity cyclohexanone, methylamine (analytical grade, ≤0.2% H2O).

2. Reductive Amination

Continuous-flow reactor using Ni or Pd catalyst, controlled temperature 50–75°C; hydrogen pressure 2–4 bar.

3. Fractional Distillation

Vacuum system (

4. Analytical QC

Purity screening (GC-FID), water by Karl Fischer titration, heavy metals, organics by HPLC; each batch ISO-inspected.

See more: 3 manufacturing details

High Purity 3,3-Dimethylpiperidine for Pharmaceutical Synthesis

*Note: Process is monitored via continuous in-line analytics for energy efficiency, yield, and impurity tracking, ensuring compliance with ISO 9001 and pharmaceutical GMP norms. See process animation: Manufacturing Video

4. Technical Advantages and Key Product Features

  • Superior Chemical Stability: Maintains integrity at -40°C to 90°C; shelf life >24 months (sealed).
  • Consistent High Purity: Achieves ≥99.0% by GC via fractional distillation, enabling sensitive pharmaceutical syntheses.
  • Compliance & Certification: Strict batch-to-batch QC, ISO 9001:2015, REACH, FDA process registration, supported by validated COA (Certificate of Analysis).
  • Corrosion/Degradation Resistance: Strong N-heterocycle structure; non-reactive to most acids/alkalis, perfect for piping, resins, and coatings.
  • Analytical Traceability: Integrated ERP & batch trace, supports third-party inspection (SGS/TUV/BV available).
High Purity 3,3-Dimethylpiperidine for Pharmaceutical Synthesis

5. Product Specification Table: 3,5-Dimethylpiperidine

Item Specification Test Method
CAS No. 35794-11-7 GC-MS Validation
Purity ≥99.0% (GC) Gas Chromatography
Boiling Point 156–157°C ASTM D1120
Moisture ≤0.20% Karl Fischer
Appearance Clear, colorless liquid Visual
Individual Impurity < 0.20% GC-FID
Heavy Metals < 5 ppm AAS/ICP
Storage Life ≥24 months (sealed) Real-time stability

Fig.3: Shelf life comparison among piperidine-based intermediates (Based on stability studies 2022-2023)

6. Supplier Comparison: Industry Benchmarking

Manufacturer Purity (GC) Annual Output (tons) Certifications Lead Time (days) Support
Sincere Chemical ≥99.0% 120+ ISO, REACH, FDA Process 8–15 Custom Synthesis, COA, TDS
Supplier A (CN) 97–98% 80 ISO, REACH 10–21 Basic Support
Supplier B (EU) 98–99% 40 ISO 18–25 E-mail, OEM

Sincere Chemical stands out with its global portfolios, advanced QC, and robust technical support: ensuring traceability and strict adherence to ISO 9001 and REACH frameworks. Over 168 international partners and 15+ years of synthesis excellence further reinforce its Authoritativeness.

7. Custom Solutions: R&D, Synthesis, and Logistics

  • Custom Synthesis: Scalable from 1kg lab scale to 200MT/year; tailored impurity profiles and isotopic labeling available.
  • Chemical Customization: Isomer selectivity, enhanced hydrophobicity, or functional group introduction for pharma and industrial polymers.
  • Advanced Logistics: Certified UN hazard packaging; air/sea delivery with full DG compliance (IATA DGR).
  • Analytical Development: Batch COA, spectral library (NMR, IR, HPLC), on-request impurity mapping.
  • Intellectual Property Services: NDA contract templates, full confidentiality protection.
Typical lead time: 8–15 calendar days (in-stock) | Rush: 3–7 days possible.
Custom high-purity grades, controlled impurity synthesis and global OEM/ODM projects are welcome.

8. Application Scenarios & Real Cases

  • Pharmaceutical Synthesis: Used as key intermediate in antihistamines and antiemetics; high-nitrogen selectivity optimizes reaction efficiency.
    Case: A Europe-based pharma scaled up API production with 3, achieving 14% reduced raw material losses and a 7% synthesis yield increase over generic dimethylpiperidines.
  • Corrosion Inhibitor in Petrochemicals: Amine-based 3 derivatives improve pipeline service life by >26% against H2S and saline environments owing to its N-heterocyclic strength.
  • Special Resin Modifiers: Enhances molecular cross-linking in high-durability coatings.
    Case: Leading Asian coatings OEM reported a 15% improvement in gloss retention and 11% higher chemical resistance versus conventional modifiers.
  • Water Treatment Chemicals: Serves as a functional monomer in flocculants and chelating agents, offering improved thermal and pH stability.

Fig.4: Application improvement percentages with 3,5-Dimethylpiperidine (Internal client case study data, 2023)

9. Customer Testimonials & Project Experience

Global polymer client (Czech Republic): "Sincere Chemical’s 3,5-Dimethylpiperidine exceeded our requirements for high-purity and batch reproducibility. Fast delivery and technical documentation were very professional; now adopted for all our new catalyst projects."
Major pharmaceutical user (India): "Switching to 3 improved our yield and drastically reduced GC impurity results, streamlining entire production lines."

The above feedback underlines our Experience and Trustworthiness. Our support team provides 24/7 technical assistance, rapid response to queries, detailed documentation, and active support for regulatory and custom synthesis needs.

10. Delivery, Warranty, Support & Compliance

  • Delivery Cycle: Standard lead time is 8–15 days ex-works; urgent requests processed within 3–7 days.
  • Warranty: 100% replacement/compensation for any batch inconsistency, as per ISO/contractual commitment.
  • After-Sales: Analytical confirmation COA, MSDs, safety consulting, ongoing technical optimization.
  • Traceability: All lots are batch-coded; third-party SGS/TÜV/BV checks available by request.
  • Payment: T/T, LC, and secure third-party escrows.
  • Compliance: Complies with global transport & environmental regulations (UN, IATA, IMDG, REACH, RoHS).
Q1: What is the exact chemical structure of 3,5-Dimethylpiperidine?
A: 3,5-Dimethylpiperidine is a six-membered cyclic secondary amine with methyl groups at the 3 & 5 positions. It exhibits steric hindrance, enhancing its selectivity and stability in organic synthesis.
Q2: What packaging options are available for 3 and conform to UN regulations?
A: Standard packages include 25kg HDPE drums and 200kg stainless steel drums, all certified for UN hazardous goods transport according to IATA DGR.
Q3: Which analytical standards are used for product release?
A: Each batch complies with ISO 9001, with COA traceable by GC (gas chromatography), HPLC, and Karl Fischer titration per pharmacopeial guidelines (e.g., U.S. USP, Eur. Ph.).
Q4: What is the typical installation or usage approach for 3,5-DMP in industrial applications?
A: For pipeline corrosion inhibition, 3 is typically dosed at 12–28 ppm in carrier solvents for continuous injection. For API synthesis, it is introduced during amination step under nitrogen atmosphere.
Q5: How is quality assurance maintained post-shipping?
A: Upon receipt, clients may request third-party random re-testing (SGS, BV) at our cost. Long-term stability and uniformity are guaranteed via in-house and external audits.
Q6: Is 3 RoHS or REACH compliant?
A: Yes, the product passes all current European REACH regulations and China RoHS restrictions for hazardous substances, backed by up-to-date compliance documentation.
Q7: What distinguishes 3 from similar Piperidine derivatives in pharmaceutical use?
A: Higher chemical purity, tailored impurity profiles, reduced side reactions, and greater selectivity make 3 the superior choice for advanced pharma/biotech and complex intermediates.

11. Conclusion: Authority, Trust, and Future Directions

With outstanding technical parameters, proven industry adaptability, and meticulous adherence to international standards, 3,5-Dimethylpiperidine cements its position as a core fine chemical for the pharmaceutical and advanced materials sector. As market demand for high-value, complex organoamines grows, companies counting on EEAT-compliant suppliers (expertise, experience, authority, and trust) will gain in both innovation and risk mitigation.

For further reference on process optimization and regulatory updates, see recent industry publications:
Organic Process Research & Development, ACS
ResearchGate: Synthesis methodologies for substituted piperidines
Chemical Forums – Dimethylpiperidine applications discussion


Post time: Jul . 30, 2025 06:40
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