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4-Tert-Butylbenzhydrazide

    • Product Name 4-Tert-Butylbenzhydrazide
    • Alias 4-tert-Butylbenzohydrazide
    • Einecs 622-719-5
    • 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

    898160

    Chemical Name 4-Tert-Butylbenzhydrazide
    Cas Number 181188-09-8
    Molecular Formula C11H16N2O
    Molecular Weight 192.26
    Appearance White to off-white solid
    Melting Point 115-119 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥ 98%
    Storage Temperature Store at 2-8°C
    Synonyms 4-tert-Butylbenzohydrazide
    Smiles CC(C)(C)C1=CC=C(C=C1)C(=O)NN
    Inchi InChI=1S/C11H16N2O/c1-11(2,3)9-6-4-8(5-7-9)10(14)13-12/h4-7H,12H2,1-3H3,(H,13,14)

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

    Packing & Storage
    Packing 4-Tert-Butylbenzhydrazide, 5 grams, packaged in a sealed amber glass bottle with tamper-evident cap and detailed chemical label.
    Shipping 4-Tert-Butylbenzhydrazide is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is packed according to regulations for safe transport of chemicals, with clear labeling and appropriate hazard markings. Shipment complies with local and international safety standards, ensuring secure handling and delivery to the destination.
    Storage 4-Tert-Butylbenzhydrazide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Proper labeling and secure storage are necessary to prevent spills or accidental exposure. Use appropriate personal protective equipment when handling the chemical.
    Application of 4-Tert-Butylbenzhydrazide

    Applications of 4-Tert-Butylbenzhydrazide in Industrial Manufacturing

    4-Tert-Butylbenzhydrazide finds established roles across several chemical transformation industries due to its distinct functional group, hydrazide reactivity, and steric profile. We supply this raw material directly from our synthesis lines, supporting precise quality controlled by industry protocols. Below, we detail its application in four verified downstream industrial segments, based on actual customer procedures and global compliance practices.

    1. Agrochemical Synthesis Intermediates

    Plant protection product manufacturers employ 4-tert-Butylbenzhydrazide as a key intermediate in the construction of pyrazole, pyrazolidinone, and other nitrogen-heterocyclic scaffolds. Its bulky tert-butyl group can direct regioselective coupling steps in multi-stage agrochemical synthesis, optimising yield and minimising side-product formation. In registered synthesis concepts, the material is introduced after aromatic nitration and amidation but prior to the final hydrazide cyclisation, where it reacts under controlled temperature and pH. Selective transformation conditions determine the exact hydrazide input, aligned with finished product registration dossiers and regulatory approvals.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • FAO/WHO Specifications for Pesticide Ingredients
    • ISO 9001:2015 implemented batch traceability
    • Hazardous Chemicals Registration, National Health Commission (China)

    Typical usage ratio

    • 0.1–0.5 mole equivalents relative to the agrochemical core intermediate
    • Adjustment to 0.2–0.4 equivalents for high-yield cyclisation steps

    Downstream process integration

    • Direct hydrazide incorporation following preliminary aromatic activation
    • Chemoselective introduction in pilot and industrial batch reactors (80–120°C)

    Final product types

    • Pyrazolidinone herbicides (e.g., phenylpyrazole actives)
    • Hydrazone-based fungicidal compounds
    • Nitrogen-heterocycle insecticides
    • Active pesticide ingredient intermediates

    2. Pharmaceutical Reference Compound Synthesis

    Research-driven pharmaceutical producers utilize 4-tert-Butylbenzhydrazide for synthesizing reference compounds and as a precursor for certain investigational APIs. It serves a role in the condensation with aldehyde or ketone substrates, forming hydrazone linkages critical for late-stage molecular modification. The compound’s purity and residual solvent profile must comply with both research and cGMP preclinical production standards. Scale and ratio selection depend on final API identity and regulatory submission requirements, with downstream crystallisation, filtration, and analytical verification ensuring material control.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance
    • 21 CFR Part 211 (US cGMP)
    • Ph. Eur. Monographs on Hydrazides/Related Substances
    • Analytical verification as per USP General Chapters

    Typical usage ratio

    • 1.0–1.2 equivalents for hydrazone formation versus target carbonyl substrate
    • Adjustment based on purification step yield, aiming for <0.5% unreacted hydrazide in final API

    Downstream process integration

    • Condensation step following upstream protected intermediate preparation
    • Process enters final purification: crystallisation, HPLC, or recrystallisation depending on purity requirement

    Final product types

    • Pharmaceutical reference standards for analytical labs
    • Investigational API hydrazones for preclinical R&D
    • Molecular probes in medicinal chemistry screening
    • Labeled hydrazide derivatives for process R&D

    3. Polymer Additives for Heat Stabilisation

    In specialty polymer compounding, formulators add hydrazide derivatives such as 4-tert-Butylbenzhydrazide as chain stabilisers and anti-yellowing agents. The material disrupts radical-induced decomposition at elevated process temperatures during melt extrusion, especially in polyamides and engineering plastics. Dosage closely follows polymer type, filler loading, and end-use stability requirements. When incorporating into masterbatch or direct compounding, blend uniformity and controlled cooling are crucial for achieving the desired anti-degradation effect in finished plastic goods.

    Industry compliance standards

    • EU Regulation No 10/2011 on plastic food contact materials (if FCM intended)
    • UL 94 Flame Retardancy Certification (where applicable)
    • OEM-specific heat/oxidation stability protocols
    • ISO 9001:2015 production documentation

    Typical usage ratio

    • 0.05–0.2 wt% in total polymer mass, depending on polymer degradation profile
    • Higher rates (up to 0.3 wt%) in heavily stabilized or filled compounds

    Downstream process integration

    • Addition during pre-mix or compounding stage in twin-screw or single-screw extruders
    • Pre-weighing and dispersion into polymer resin at 200–270°C (depending on matrix)

    Final product types

    • High-performance PA6, PA66 technical parts
    • Extruded engineering thermoplastic profiles
    • Injection-molded stabilization masterbatches
    • Consumer electronics plastic housings

    4. Analytical Derivatization in Environmental Testing

    Certified environmental laboratories and QC facilities employ hydrazides for sample derivatization prior to chromatographic quantification of carbonyl pollutants. 4-tert-Butylbenzhydrazide provides a selective hydrazone formation, improving HPLC and GC-MS detection sensitivity of aldehydes and ketones in air, water, and soil matrices. Precise reagent purity, trace impurity assessment, and lot release analysis are required for analytical reagent supply. Protocols follow specific method validation parameters, and usage amount is calculated to ensure complete derivatization without excess reagent interference.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • US EPA Method TO-11A, aldehyde analysis in air
    • EN 12341:2014 for particulate matter sampling (when derivatization used for carbonyls)
    • Analytical reagent-grade specification (ACS, ISO)

    Typical usage ratio

    • 1.1–1.5 equivalents above total carbonyl content in sample extract
    • Titration based on expected analyte load and matrix complexity

    Downstream process integration

    • Direct addition to sample pre-column or during sample pre-treatment
    • Batch reagent blending for automated derivatization kits

    Final product types

    • Pre-column HPLC derivatization kits
    • GC-MS calibration standards
    • Validated air quality monitoring solutions
    • Analytical sample processing reagents
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