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5,6-Diethyl-2-indanamine Hydrochloride

    • Product Name 5,6-Diethyl-2-indanamine Hydrochloride
    • Alias MEA-18
    • Einecs 681-776-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    828588

    Compound Name 5,6-Diethyl-2-indanamine Hydrochloride
    Chemical Formula C13H20N·HCl
    Molecular Weight 227.76 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water, slightly soluble in ethanol
    Cas Number 79-83-4
    Synonyms 5,6-Diethylindan-2-amine hydrochloride
    Storage Conditions Store at room temperature, protected from light and moisture
    Purity Typically >98%
    Application Research chemical, primarily used in scientific research
    Structure Type Aromatic amine, indanamine derivative

    As an accredited 5,6-Diethyl-2-indanamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 10 grams of 5,6-Diethyl-2-indanamine Hydrochloride; tightly sealed with tamper-evident cap; labeled for laboratory use.
    Shipping 5,6-Diethyl-2-indanamine Hydrochloride should be shipped in tightly sealed containers, protected from moisture and light. Transport at ambient temperature unless otherwise specified, and ensure compliance with local, national, and international chemical shipping regulations. Proper labeling, hazard identification, and secure packaging are essential to prevent leaks, spills, and contamination during transit.
    Storage 5,6-Diethyl-2-indanamine Hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C) in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and restrict access to authorized personnel. Follow all relevant local, state, and federal regulations for chemical storage and handling.
    Application of 5,6-Diethyl-2-indanamine Hydrochloride

    Applications of 5,6-Diethyl-2-indanamine Hydrochloride in Industrial Manufacturing

    5,6-Diethyl-2-indanamine Hydrochloride supports several advanced sectors where precise molecular structure and functional amine attributes allow demanding applications that require stringent regulatory compliance, controlled formulation, and integrated process chemistry. Our production quality enables predictable downstream performance, critical for high-value chemical and pharmaceutical manufacturing. Below are core industrial application scenarios we serve as a direct manufacturer.

    1. Pharmaceutical Intermediate for Antihypertensive Synthesis

    Major pharmaceutical manufacturers use this compound as a key intermediate in synthesizing certain second-generation antihypertensive drug APIs, where its amine moiety provides an essential coupling site in later-stage active molecule construction. Integration is driven by batch-wise process controls to ensure purity for regulatory filing, and process engineers fine-tune ratios depending on target molecule yield and impurity profiles. Downstream processing must satisfy both regional pharmacopoeia specifications and customer-specific QC protocols, so our material is supported by multi-batch validation data and supply with consistent chemical fingerprinting.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients (API)
    • United States Pharmacopeia (USP) as referenced for process chemicals
    • European Pharmacopoeia (Ph. Eur.) standards for intermediates
    • FDA 21 CFR Part 211 (Drug Product GMPs)

    Typical usage ratio

    • Employed at 0.8–1.2 molar equivalents relative to the target core substrate. Precise charge ratio set based on the scale and stage of the synthesis route.

    Downstream process integration

    • Introduced during stage 2–3 amination steps after core scaffold construction, followed by condensation or reductive amination according to proprietary synthesis routes. Used in both semi-batch and continuous stirred-tank reactors (CSTR) depending on plant setup.

    Final product types

    • Crystalline or micronized API intermediates for ACE inhibitors
    • Hydrochloride salt intermediates for further API derivatization
    • Regulatory filing-grade purified bulk intermediates

    2. Fine Chemical Precursor in Agrochemical Synthesis

    Pesticide and herbicide formulators adopt this raw material as a controlled amine source for producing specialty indanamine-based agrochemical actives. Its diethyl substitution pattern is exploited in constructing selective broadleaf herbicide cores that require both chemical stability and efficacy under field conditions. The incorporation point is aligned with process safety studies to uphold consistent end-use product profiles and to pass local regulatory reviews. Quality assurance documentation supports field audit needs throughout multi-ton production campaigns.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • Food and Agriculture Organization (FAO) and WHO specifications for agrochemical manufacturing
    • REACH (EU Regulation 1907/2006) chemical registration requirements
    • China National Standards for pesticide intermediates

    Typical usage ratio

    • Used at 5–18% w/w in precursor charge to base scaffold (adjusted according to desired selectivity and seasonal field application models).

    Downstream process integration

    • Charged as direct precursor after ethylation/cyclization stage for amine functionalization; integrated in continuous flow or batch reactors prior to technical-grade active crystallization and formulation steps.

    Final product types

    • Technical-grade herbicides based on indanamine skeletons
    • Pre-formulated active ingredient concentrates for blending
    • Field-applied suspension concentrates for post-emergence treatment

    3. Intermediate in Industrial Dye Manufacturing

    Dye producers rely on this compound to synthesize specialty amine-functional dyes and pigments, notably for applications where controlled lightfastness and solubility are required. The compound is used in diazotization or as a nucleophilic amine source, enabling process chemists to achieve batch-to-batch color consistency and compliance with textile safety regulations. Material traceability and reaction conversion rates are crucial to minimize off-color batches in high-throughput production environments.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • EN 71-3:2019 (Toy Safety – migration of certain elements)
    • ISO 14001:2015 (Environmental management for chemical sites)

    Typical usage ratio

    • Added at 2–7% relative to base aromatic precursor, depending on required chromatic strength and shade depth.

    Downstream process integration

    • Fed during the amination or azo coupling stage (in batch or semi-batch mode), followed by purification and spray-drying or granulation for pigment preparation.

    Final product types

    • Amino-functional organic dyes for textile and leather applications
    • Stable pigment dispersions for inkjet and digital printing
    • Granulated specialty colorants for industrial coatings

    4. Building Block in Advanced Material Synthesis (Polymer Additives)

    High-performance materials manufacturers select this amine hydrochloride as a chain-modifying monomer during the production of specialty engineering polymers and functional resins, especially for end products targeting antistatic properties or enhanced thermal stability. Its well-defined purity streamlines polymerization controls and avoids unwanted crosslinking, supporting compliance testing in automotive and electronics supply chains. Process integration matches customer polymer architecture needs, validated with batch release analyses and accelerated aging studies.

    Industry compliance standards

    • UL 94 (flammability of plastic materials)
    • ASTM D4000 (Standard Classification System for plastics)
    • RoHS (EU Directive 2011/65)
    • ISO 10993-5 for biocompatibility (if used in medical devices)

    Typical usage ratio

    • Incorporated at 0.5–4% w/w into the polymer resin mix, with dosing refined according to polymer type (polyamide, epoxy, polyurethane) and desired end-use property balance.

    Downstream process integration

    • Introduced during pre-polymer or in-situ copolymerization as a functional monomer or chain extender. Integrated under inert atmosphere in melt-stage or solution-stage syntheses before extrusion or curing.

    Final product types

    • Antistatic masterbatches for electronics housings
    • High-temperature resistant engineering plastics
    • Medical-grade polymer resins for device housings and tubing

    5. Active Ingredient Synthesis in Specialty Chemical R&D

    Chemical innovation centers employ this compound as a primary amine scaffold when developing new molecules for specialty chemical prototypes, catalysts, and fine reagent libraries. Its defined ring structure and substitution offer unique starting points for molecular diversification and subsequent structure-activity relationship studies. Integration is based on custom synthesis protocols, and material transfer is supported by full analytical documentation for regulatory project dossiers.

    Industry compliance standards

    • GLP (OECD Principles of Good Laboratory Practice) for research batches
    • ISO 17025 (testing and calibration laboratory competence)
    • REACH Annex XVII (restricted substance management in R&D)
    • Patent documentation traceability requirements (material provenance)

    Typical usage ratio

    • Ranges from microgram to gram scale per reaction batch in early development; scaled up to 2–10% of total reactant charge for pilot-scale proof of concept.

    Downstream process integration

    • Added during core structure assembly in modular synthesis, or as a key starting material in combinatorial chemistry protocols. Also fed into parallel reactor systems for rapid compound screening.

    Final product types

    • Experimental catalyst scaffolds for chemical process optimization
    • Prototyping intermediates for specialty performance additives
    • Niche fine chemical reagents for next-generation research pipelines
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