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2-Carboxybenzaldehyde

    • Product Name 2-Carboxybenzaldehyde
    • Alias 2-Formylbenzoic acid
    • Einecs 208-943-6
    • 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

    244801

    Iupac Name 2-Formylbenzoic acid
    Molecular Formula C8H6O3
    Molar Mass 150.13 g/mol
    Cas Number 119-67-5
    Appearance White to off-white crystalline powder
    Melting Point 137-141 °C
    Density 1.36 g/cm³
    Solubility In Water Slightly soluble
    Smiles C1=CC=C(C(=C1)C=O)C(=O)O
    Pubchem Cid 8718
    Refractive Index 1.630 (predicted)

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

    Packing & Storage
    Packing 2-Carboxybenzaldehyde, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with hazard and handling information.
    Shipping 2-Carboxybenzaldehyde is shipped in tightly sealed containers, protected from moisture and incompatible substances. The chemical must be properly labeled and accompanied by a safety data sheet (SDS). Shipping complies with relevant regulations for hazardous materials, ensuring safe handling during transport and storage to prevent leaks, spills, or exposure.
    Storage 2-Carboxybenzaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Use proper personal protective equipment when handling, and label the storage area clearly to prevent accidental exposure or misuse.
    Application of 2-Carboxybenzaldehyde

    Applications of 2-Carboxybenzaldehyde in Industrial Manufacturing

    2-Carboxybenzaldehyde serves as an essential fine chemical intermediate in multiple downstream industrial fields. As a direct manufacturer, we support specialized applications in pharmaceuticals, dyes, specialty polymers, corrosion inhibitor synthesis, and agricultural formulations, supplying high-purity product meeting strict global requirements.

    1. Pharmaceutical Intermediate for Cephalosporin Antibiotic Synthesis

    2-Carboxybenzaldehyde acts as a building block in the preparation of cephalosporin core intermediates, especially in the synthesis of 7-ACA (7-aminocephalosporanic acid) derivatives. Downstream pharmaceutical producers use it in regulated multi-step processes to introduce functional side-chains on cephalosporin backbones. Typical processes require stringent raw material traceability and batch consistency, with full documentation for regulatory submission. Integration occurs at the amide-functionalization or side-chain modification stages under strictly controlled conditions, and the downstream output feeds into the manufacture of advanced injectable or oral antibiotic products for hospital and retail markets.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) under 21 CFR Parts 210/211
    • Chinese Pharmacopoeia (ChP), European Pharmacopoeia (Ph. Eur.), United States Pharmacopeia (USP)
    • EDQM CEP and FDA DMF filing requirements
    • ICH Q7 for Active Pharmaceutical Ingredient (API) intermediates

    Typical usage ratio

    • Applied at 0.12–0.25 molar equivalent relative to β-lactam starting material. Precise usage depends on cephalosporin derivative; adjusted based on kinetic monitoring and residual aldehyde analysis.

    Downstream process integration

    • Introduced following core β-lactam ring formation.
    • Employed as a key side-chain precursor in amidation or acylation stages, under inert gas, in polar aprotic solvents.
    • Integrated into automated reactor systems equipped with in-line HPLC for purity control.

    Final product types

    • Ceftriaxone sodium sterile API
    • Cefotaxime bulk powder
    • Third-generation cephalosporin injectables
    • Oral cephalosporin antibiotic tablets and capsules

    2. Intermediate for Azo and Anthraquinone Dye Manufacturing

    In the industrial dye sector, 2-Carboxybenzaldehyde enables the formation of complex aromatic frameworks through condensation, cyclization, and coupling reactions. It is especially utilized for preparing anthraquinone derivatives and high-performance azo dyes used in textile and synthetic fiber coloration. The material must meet strict content and impurity specifications, allowing downstream partners to ensure colorfastness, shade reproducibility, and heavy metal compliance. Addition occurs at coupling or ring-closure stages, frequently in jacketed batch reactors with automated temperature and pH controls to ensure consistent pigment characteristics. End products are tested for resistance to washing, light, and elevated temperatures as required for apparel and industrial applications.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • REACH Annex XVII dye and pigment restrictions
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 105-B02, 105-C06 (color fastness tests)

    Typical usage ratio

    • Typically 0.08–0.16 molar equivalent relative to primary amine component, based on desired shade intensity. Adjusted as per specific dye chemistry.

    Downstream process integration

    • Added in coupling sequence to react with aromatic diamines or hydrazines.
    • Outsourced for ring-closure reactions in anthraquinone synthesis under controlled pH and temperature, followed by crystallization or spray drying.
    • Used in pigment modification stages for fine-tuning dye solubility and dispersion properties.

    Final product types

    • Reactive azo dyes for cotton and cellulosic fibers
    • Disperse anthraquinone dyes for polyester fiber
    • High-performance pigments for plastics and specialty coatings
    • Printing inks for textiles and packaging

    3. Specialty Polymer Material Synthesis (Polyimides & Polyesters)

    Advanced polymer manufacturers use 2-Carboxybenzaldehyde as a monomeric precursor in producing polyimide and polyester resins with precise molecular architecture. Its incorporation imparts rigidity and enhances thermal stability in high-performance materials, especially for electronic insulation, automotive, and aerospace applications. Compliance with material safety and purity is documented throughout the process, with real-time monitoring for traces of unreacted aldehyde and color impurities. The product is introduced in stoichiometric balance with diamine or diol components in melt-phase or solvent-based polymerizations. Process control focuses on end-group functionality to meet downstream customers’ specifications for dielectric, mechanical, and optical performance.

    Industry compliance standards

    • UL 94 flammability classification
    • RoHS 2011/65/EU (for electronic materials)
    • ISO 9001 and IATF 16949 (automotive quality management)
    • IEC 60216-1 (thermal endurance requirements)

    Typical usage ratio

    • Used at 1:1 molar ratio with primary diamine (polyimide) or diol (polyester) component. Ratios may be fine-tuned ±5% depending on desired end-group functionality and molecular weight target.

    Downstream process integration

    • Charged at the polymerization pre-condensation stage in specially lined reactors.
    • Integrated in co-polymerization with controlled heating profiles and vacuum stripping to minimize residual monomer content.
    • Subject to in-process FTIR and GPC monitoring for molecular structure verification.

    Final product types

    • High-temperature polyimide films and varnishes
    • Apparel-grade polyester specialty fibers
    • High-strength composite resins
    • Electrical insulation laminates for printed circuit boards

    4. Synthesis of Benzimidazole-Based Corrosion Inhibitors

    The chemical is a precursor in the industrial synthesis of benzimidazole derivatives used as corrosion inhibitors for metal processing fluids, cooling water systems, and closed-loop heating installations. Its use enables the formation of aromatic ring systems exhibiting strong metal surface adsorption and film-forming properties. Production requires strict batch documentation and impurity control to comply with environmental guidelines for downstream applications. Manufacturers add this material in pre-cyclization steps under catalytic conditions, monitoring conversion and purity prior to blending with other inhibitor components. Finished inhibitor formulations must pass laboratory corrosion rate and compatibility tests relevant to their intended service environments before commercial shipping.

    Industry compliance standards

    • ISO 8044:2019 (corrosion terminology and definition)
    • ASTM D1384 (engine coolant corrosion test)
    • REACH compliance for downstream water treatment chemicals
    • EN 13094 (safety in storage and handling of chemicals for water applications)

    Typical usage ratio

    • Added at 0.1–0.2 molar equivalent with respect to amine cyclization partner; formulation concentration in final inhibitor product ranges 0.5–2% w/w according to field performance demands.

    Downstream process integration

    • Charged in closed-loop reactors fitted with pH monitoring and reflux systems during cyclization.
    • Combined with additional functionalized alcohols or amines to modulate metal affinity and solubility.
    • Integrated into multi-component blends and QC-checked for compatiblity and chemical stability.

    Final product types

    • Water-soluble corrosion inhibitor concentrates for industrial water systems
    • Multi-purpose rust inhibitor formulations for automotive and machinery fluids
    • Protective additives for oil and gas pipeline chemicals
    • Closed-circuit heating and cooling corrosion control blends

    5. Active Ingredient Intermediate for Plant Growth Regulator Formulation

    In the agrochemical sector, downstream partners utilize 2-Carboxybenzaldehyde to synthesize plant growth regulators for crop protection and yield enhancement. Integrators require a highly pure, low-residue input, as regulatory controls on trace impurities are rigorous. The intermediate enters plant growth regulator synthesis at ring-closure or side-chain modification points, where it reacts under mild catalysis to deliver active molecules with targeted bioavailability. The process adheres to agrochemical batch tracing, and product undergoes multi-residue screening prior to formulation and field application. Finished agrochemical formulations subsequently must be registered and tested for crop safety and environmental fate in compliance with international agricultural standards.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001 with traceable batch recording for agrochemical QA
    • EU Regulation (EC) No 1107/2009 (plant protection products)
    • US EPA 40 CFR Part 180 (Tolerance for Residues)

    Typical usage ratio

    • Generally 0.09–0.22 molar equivalent during key condensation steps. Downstream usage in formulated product commonly 1–5% w/w, modified per specific crop and local application protocols.

    Downstream process integration

    • Employed at condensation and cyclization stages within closed reactor systems.
    • Converted in situ into heterocyclic intermediates, then isolated for subsequent blending with adjuvants and safeners.
    • Final integration into soluble granules, suspension concentrates, or emulsifiable concentrates based on regional agricultural product forms.

    Final product types

    • Plant growth regulator technical concentrates
    • Field-ready crop growth enhancement formulations
    • Rice, corn, and wheat-specific application packages
    • Plant metabolic stimulation agents for horticulture
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