Enterprise API & Intermediate Dossier

China Cas 119276-01-6 Manufacturer & Factories

Direct Industrial-Scale Synthesis, Validated GMP Quality Systems, and Resilient Global Supply Pipelines for 4,4'-(1H-1,2,4-Triazol-1-ylmethylene)dibenzonitrile (Letrozole Intermediate / Active Precursor).

Primary Catalog Dispatch

High-Purity Reference APIs & Synthesized Precursors

Procurement teams evaluate these high-yield compounds for stringent pharmaceutical research, API formulation, and batch manufacturing compliance.

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Industrial Whitepaper Dossier

Chemical Identity & Strategic Value of CAS 119276-01-6

An authoritative technical evaluation of 4,4'-(1H-1,2,4-triazol-1-ylmethylene)dibenzonitrile, the cornerstone precursor for non-steroidal third-generation aromatase inhibitors.

≥ 99.5%
HPLC Assay Purity
Controlled Chromatographic Threshold
< 0.10%
Single Unknown Impurity
Strict ICH Q3A/B Alignment
50 MT+
Annual Capacity
Scalable Hebei Facility Synthesis
100%
Traceability Index
COA, NMR, and LC-MS per Batch
Analytical Parameter Enterprise Specification Benchmark USP / Ph. Eur. Method Reference Release Status
Chemical Nomenclature 4,4'-(1H-1,2,4-Triazol-1-ylmethylene)dibenzonitrile IUPAC / Systematic Standard Certified
CAS Registry Number 119276-01-6 Chemical Abstracts Service Validated
Molecular Formula & Weight C17H11N5 · 285.31 g/mol High-Resolution MS Identity Exact Match
Physical State & Appearance White to off-white crystalline solid, odorless Visual & Optical Microscopy Conforms
Melting Range 181.0 °C – 184.5 °C Capillary Melting / DSC Thermal Method Within Spec
Chromatographic Purity (HPLC) ≥ 99.5% (Isocratic & Gradient Verified) Ph. Eur. 2.2.29 / Reverse-Phase C18 Premium Grade
Heavy Metal & Elemental Impurities Lead (Pb) ≤ 2ppm, Arsenic (As) ≤ 1ppm, Total ≤ 10ppm ICP-MS (USP <232> / <233>) Ultra-Low
Residual Solvents Profile Methanol < 3000ppm, Toluene < 890ppm, DCM < 600ppm Headspace Gas Chromatography (GC-FID) Compliant
Supply Chain Intelligence

Global Enterprise Sourcing Architecture for CAS 119276-01-6

Macro-industry dynamics dictate that pharmaceutical formulators, CDMOs, and generic medicine manufacturers eliminate supply vulnerabilities via direct synthesis partnerships.

Supply Chain Resiliency

Global oncological pipelines cannot tolerate regulatory suspensions or batch recalls caused by unstable precursors. We control starting materials — 4-bromomethylbenzonitrile and 1,2,4-triazole — guaranteeing uninterrupted upstream supply independent of external third-party market fluctuations.

Genotoxic Impurity Suppression

Alkylating and triazole-based process intermediates pose genotoxic risks under ICH M7 guidelines. Our industrial-scale crystallization protocols systematically purge trace halogenated precursors down to sub-threshold concentrations, eliminating costly regulatory holds for drug substance filers.

Complete Regulatory Auditing

Every commercial order is backed by full analytical dossiers including 1H-NMR, 13C-NMR, FT-IR, HPLC chromatograms, GC residual solvent analysis, and structural confirmation. We provide Certificate of Origin, SDS (OSHA/CLP compliant), and formal DMF Type II support documentation.

Engineering Excellence

Industrial Synthesis Route & Batch Production Flow

A multi-stage chemical engineering sequence engineered in Shijiazhuang, Hebei, delivering maximum selectivity, optimized reaction kinetics, and minimum carbon impact.

PHASE 01

Starting Material Activation

Rigorous quality screening of bis(4-cyanophenyl)methanol derivatives or 4-(bromomethyl)benzonitrile with precise stoichiometric baseline validation.

PHASE 02

Heterocyclic Triazole Coupling

Regioselective nucleophilic substitution incorporating 1,2,4-triazole under mild alkaline conditions, suppressing unwanted regioisomeric side-products.

PHASE 03

Preparative Isolation

Liquid-liquid extraction followed by organic phase washing to remove inorganic salts and trace unreacted starting reagents under vacuum control.

PHASE 04

Precision Recrystallization

Multistage solvent crystallization using pharmaceutical-grade alcohols to lock in precise polymorph stability and eradicate residual colorants.

PHASE 05

Vacuum Drying & Packaging

Low-temperature rotary conical drying, inert nitrogen purging, sealed anti-static foil containment, and QA release against strict COA benchmarks.

Future-Proof Manufacturing

Technical Roadmap & Sustainable Production (2026–2030)

Continuous process improvement, Process Analytical Technology (PAT), and green chemistry paradigms ensure global competitiveness and zero supply disruptions.

Continuous Flow Microreactors

Transitioning from conventional batch reactors to modular continuous flow micro-reaction systems. This transition drastically reduces residence time, eliminates localized hotspots, and ensures that critical parameters (temperature, pH, pressure) remain within ±0.1% tolerances throughout multi-ton campaigns.

AI-Powered Crystallization Modeling

Employing machine learning models trained on nucleation kinetics and crystal growth data to predict polymorphism under variable cooling gradients. This guarantees precise particle size distribution (D50, D90) tailored for direct downstream tablet compression without secondary micronization.

Circular Solvent Closed-Loop Systems

Implementing membrane vapor permeation and automated distillation columns achieving >95% solvent recovery. By decoupling raw chemical inputs from volatile petrochemical pricing, Hebei Miaoou delivers fixed-price supply stability across multi-year procurement contracts.

Export & Localization

Global Logistics, Customs Assurance & Packaging Protocols

End-to-end cold-chain and standard chemical logistics engineered for compliant importation across North America, Europe, LATAM, and Asia-Pacific.

UN-Rated
Industrial Packaging
1kg, 5kg, 25kg Fibre Drums
DDP / CIF
Flexible Trade Terms
Customs Brokerage Handled
24h
Rapid Dispatch Response
Warehoused Inventory Clearance
Zero Loss
Anti-Tamper Protocol
Vacuum Foil Double PE Liner

Ready to Audit Our Hebei Synthesis Facility?

Hebei Miaoou Technology Co., Ltd. (operating since 2010) welcomes both on-site enterprise audits and third-party QA inspections (SGS, Intertek, Eurofins). Request our master facility dossier, sample batch COAs, and raw spectroscopic data.

Shijiazhuang, Hebei, China +852 9862 1364 [email protected]
Technical & Commercial Intelligence

Frequently Asked Questions by Sourcing Directors

Comprehensive technical and commercial clarity regarding CAS 119276-01-6 synthesis, testing benchmarks, and cross-border delivery.

What is the specific pharmaceutical utility of CAS 119276-01-6?

CAS 119276-01-6 is chemically known as 4,4'-(1H-1,2,4-triazol-1-ylmethylene)dibenzonitrile. It represents the central active molecular core and principal synthetic precursor for Letrozole, an established third-generation aromatase inhibitor extensively manufactured for hormone receptor-positive oncology treatments and reproductive endocrinology research.

How does your factory control the regioisomeric 4H-1,2,4-triazole impurity?

During the alkylation coupling stage, the formation of the unwanted 4H-[1,2,4]-triazol-4-yl isomer is suppressed via proprietary low-temperature kinetic control combined with polar aprotic solvent optimization. Any residual isomer is selectively partitioned out in the recrystallization mother liquor, guaranteeing final levels below 0.05% by HPLC.

What analytical documentation accompanies each production batch?

Every shipment is released with a comprehensive, batch-specific Certificate of Analysis (COA). Standard dossiers include HPLC chromatograms (with relative retention times and peak areas), 1H-NMR spectrum, LC-MS molecular weight confirmation, Karl Fischer water titration, residual solvent GC data, and heavy metal ICP-MS scan.

Can you accommodate custom particle size distribution (PSD) requirements?

Yes. In addition to our standard crystalline powder format, we operate clean-room jet milling systems capable of producing tailored micronized grades (e.g., D90 < 20μm or D50 between 5–10μm) tailored specifically to your direct tablet compression or wet granulation operational parameters.

What are the minimum order quantities (MOQ) and scalable packaging formats?

We support trial quantities for R&D pilot validation starting at 100g and 1kg in vacuum-sealed double polyethylene aluminum foil pouches. For commercial industrial manufacturing, standard packaging is 25kg UN-rated tamper-evident fiber drums with multi-layer nitrogen-flushed barrier liners.

How are international customs, duties, and freight clearance managed?

Hebei Miaoou Technology maintains established export routes servicing the US, UK, European Union, India, Brazil, and Southeast Asia. We offer flexible Incoterms including EXW, FOB, CIF, and full Delivered Duty Paid (DDP) where our logistics desk executes customs clearance, duty settlement, and door-to-door delivery.

Extended Synthesis Range

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