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4-Dimethylamino-2-Methoxybenzaldehyde

    • Product Name 4-Dimethylamino-2-Methoxybenzaldehyde
    • Alias Ehrlich's Reagent
    • Einecs 204-304-2
    • 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
    VTB
    Specifications

    HS Code

    794849

    Cas Number 1008-72-6
    Molecular Formula C10H13NO2
    Molecular Weight 179.22 g/mol
    Iupac Name 4-(Dimethylamino)-2-methoxybenzaldehyde
    Appearance Yellow to orange crystalline powder
    Melting Point 69-72°C
    Boiling Point 332.1°C at 760 mmHg
    Density 1.13 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms Ehrlich’s reagent, p-Dimethylaminoveratraldehyde
    Storage Conditions Store at 2-8°C away from light
    Smiles CN(C)c1ccc(OC)c(C=O)c1
    Refractive Index 1.587

    As an accredited 4-Dimethylamino-2-Methoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled "4-Dimethylamino-2-Methoxybenzaldehyde, 25g." Includes hazard symbols and lot number.
    Shipping 4-Dimethylamino-2-Methoxybenzaldehyde should be shipped in tightly sealed containers, protected from light and moisture. Use appropriate packaging compliant with local regulations, including labeling for hazardous chemicals. Transport at ambient temperatures, avoiding excessive heat or cold. Ensure shipping documentation includes safety and handling instructions in accordance with chemical shipping standards.
    Storage **4-Dimethylamino-2-Methoxybenzaldehyde** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep the chemical out of direct sunlight and moisture. Properly label the storage container, and restrict access to trained personnel. Use appropriate secondary containment to prevent accidental spills or leaks.
    Application of 4-Dimethylamino-2-Methoxybenzaldehyde

    Applications of 4-Dimethylamino-2-Methoxybenzaldehyde in Industrial Manufacturing

    4-Dimethylamino-2-Methoxybenzaldehyde serves as a key intermediate in specialized chemical manufacturing. Our production base supplies this raw material exclusively to regulated downstream sectors that require high-quality, traceable intermediates for formulation and final product consistency. Below we present detailed use scenarios according to actual industrial sectors.

    1. Pharmaceutical Intermediate for Synthesizing Antihistamine Compounds

    Pharmaceutical manufacturers integrate this intermediate during multi-step synthesis of certain antihistamine actives, such as dimetindene and related ethers. Downstream formulation demands high purity and defined impurity profiles, impacting final API compliance. We ensure batch-to-batch consistency suited for regulated pharmaceutical production, validated by documented release under cGMP.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • 21 CFR Part 211 (US FDA cGMPs)
    • Relevant pharmacopeia monographs (USP, EP) for final API synthesis

    Typical usage ratio

    • Typically 0.5 – 2.5 molar equivalents relative to core aminated starting materials, determined by final API stoichiometry

    Downstream process integration

    • Introduced at condensation-reaction step during the early phase of API synthesis
    • Requires purification steps to minimize side-products downstream
    • Subject to in-process controls for residual solvents/impurities
    • Delivered as a critical-reagent lot with full traceability

    Final product types

    • Finished antihistamine API bulk substances
    • Pharmaceutical oral solid dosages (tablets, capsules)
    • Parenteral antihistamine formulations
    • Research and reference standards for pharmaceutical R&D labs

    2. Chromogenic Agent in Clinical Colorimetric Analysis Kits

    Diagnostic OEMs use this compound as a specialized chromogenic aldehyde for colorimetric determination of compounds containing indole groups, for example in urobilinogen urine strip tests. Accurate measurement depends on consistent reactivity and color output, making supply chain qualification and conformance with EN and ISO standards mandatory.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices Quality Management Systems
    • EN 13612:2002 Performance Evaluation of In Vitro Diagnostic Medical Devices
    • 21 CFR Part 820 (US FDA Quality System Regulation for Medical Devices)
    • Directive 98/79/EC (IVDD) in European Union, MDR IVDR 2017/746 after 2022

    Typical usage ratio

    • Applied at 0.1 – 1.3% (w/w) in proprietary indicator systems, with the ratio fine-tuned based on substrate loading and strip chemistry

    Downstream process integration

    • Dissolved in indicator solution matrix under controlled pH conditions
    • Impregnated onto cellulose or polymer supports in test strip manufacturing
    • Subjected to accelerated stability testing in finished assay kits
    • Handled under ISO-classified clean area to maintain analytical validity

    Final product types

    • Diagnostic test strips for clinical urinalysis
    • Point-of-care kits for hospital labs
    • Colorimetric microplates for biochemistry analyzers
    • Ancillary reagent sets for automated analyzers

    3. Dye Intermediate for Speciality Azo and Triarylmethane Dyes

    Colorants industry utilizes this molecule as a tailored intermediate for high-performance dyes, where electron-donating effects influence hue and fastness. Process development teams require specific methylation and methoxylation patterns to control the final chromophore structure, directly impacting textile and inkjet dye batch approval.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for restricted substance compliance in textiles)
    • REACH Annex XVII (EU restricted dye intermediates)
    • US EPA TSCA chemical inventory inclusion
    • GMP for Dyes, Pigments and Intermediates (ZELLCHEMING)

    Typical usage ratio

    • Formulation incorporates 2–6% (w/w) depending on final dye structure and batch size; adjusted for chromophore extension or shade matching

    Downstream process integration

    • Charged to reaction with diazonium salt or benzyl chloride in core synthesis
    • Reacted under alkaline or acidic conditions to convert to respective dye precursors
    • Controlled by HPLC/UV for completeness of conversion
    • Crystallized and milled for use in pigment processing or direct dye formulation

    Final product types

    • Synthetic textile dyes (polyester, acrylic)
    • Specialty inks for inkjet printing
    • High-lightfast pigment dispersions
    • Industrial marking fluids

    4. Fine Chemical for Analytical Laboratory Reagent Synthesis

    Suppliers for analytical chemistry produce color-generating or derivatizing reagents using this aldehyde, vital for spectrophotometric quantification and HPLC sample prep. Routine QC labs in the food, water, and environmental sectors specify analytical purity and confirm origin through certificate of analysis and COA batch retention.

    Industry compliance standards

    • ISO 17025 Laboratory Quality Management
    • ACS Reagent Chemicals requirements (for analytical applications)
    • FDA Analytical Procedures and Methods Validation (21 CFR Part 211.160)
    • JIS K8001 (Japanese reagents quality standards)

    Typical usage ratio

    • Used at 0.05 – 0.25 mmol for 10–100 mL reactions, typically in excess relative to target analyte to ensure complete derivatization

    Downstream process integration

    • Reacted with primary/secondary amines in quantitative UV-Vis color determination
    • Processed into pre-mixed reagent sets for laboratory kits
    • Packaged in inert-atmosphere ampoules to preserve quality
    • Subject to rigorous batch release protocols for analytical traceability

    Final product types

    • Ready-to-use analytical reagents
    • Derivatization kits for HPLC and LC-MS
    • Reference chemicals for laboratory calibrations
    • Photometric assay reagents

    5. Synthesis of Functional Materials in Organic Electronics

    Advanced material manufacturers employ the aldehyde as a building block for synthesizing charge-transfer complexes and donor-acceptor systems used in OLEDs and organic solar cells. Structural features and electronic properties of this intermediate influence performance in electronic devices, enforcing tight process controls and materials compatibility testing.

    Industry compliance standards

    • JEDEC Standard JESD22 (organic electronics reliability tests)
    • IEC 62899 (Printed Electronics general standards)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 (quality management for functional material production)

    Typical usage ratio

    • Varies from 1–10 mol% relative to target donor-acceptor system, adjusted according to required photoelectronic property

    Downstream process integration

    • Condensed with amines or isocyanates to build π-conjugated backbones
    • Incorporated into polymerization or oligomerization steps
    • Purified by column chromatography to 99.9% purity for device compatibility
    • Processed under inert atmosphere to prevent oxidation

    Final product types

    • Emissive layers in OLED displays
    • Organic photovoltaic materials
    • Charge transport intermediates for semiconductor devices
    • Specialty polymer coatings for electronics
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