ISO 9001:2015 & cGMP Standard Chemical Intermediates

High-Quality Methyl 3-Oxo-2-Phenylbutyrate Suppliers & Products

A comprehensive technical authority guide and global supply framework for Methyl 3-Oxo-2-Phenylbutyrate (CAS 4433-88-7 / BMK Intermediate) serving certified analytical, specialty pharmaceutical, and high-precision synthesis markets.

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Technical Profile & Global Chemical Landscape

Methyl 3-oxo-2-phenylbutyrate represents a critical keto-ester platform, structurally configured for diverse asymmetric reductions, organocatalytic reactions, and advanced chemical synthesis.

≥99.2%
Assay Purity by HPLC/GC
<0.05%
Controlled Residual Moisture (KF)
50MT+
Monthly Synthesis Capacity
100%
Traceability via Spectroscopic COA
Analytical Parameter Technical Specification Benchmark Testing Methodology Significance for Industrial End-Users
IUPAC Nomenclature Methyl 3-oxo-2-phenylbutanoate IUPAC Standard Registry Exact chemical taxonomic tracking
CAS Registry Number 4433-88-7 (Isomer profile verified) CAS Chemical Indexing Regulatory clearance & export validation
Assay Purity (GC/HPLC) ≥99.0% (Single Impurity <0.2%) FID Chromatography & DAD (210nm) Prevents downstream catalytic poisoning
Physical State & Clarity Clear to pale yellowish oily liquid / viscous oil Visual / Photometric Transmission Absence of unreacted polymeric precursors
Moisture Content (Water) ≤0.10% w/w Karl Fischer Coulometric Titration Crucial for moisture-sensitive alkylation steps
Heavy Metals (Pb, Cd, Hg, As) ≤10 ppm cumulative ICP-MS Analysis cGMP pharmaceutical feedstock requirement

Regulated Precursor Control

Due to its functional keto-ester structure, international commercial transactions require compliance with domestic DEA/INCB regulatory lists and declared end-user certifications to guarantee legitimate research applications.

Global Compliance

Downstream Chemical Value

Serves as a critical foundation for chiral building blocks, resolving racemic α-aryl propanoic derivatives and providing intermediates for active research molecules across neuroscience and specialty materials.

Synthetic Intermediate

Supply Chain Vulnerability

Global availability has historically fluctuated due to shifts in customs scrutiny. Reliable procurement relies on factories maintaining direct dual-use licensing and consistent non-infringing chemical routes.

Market Continuity

Industrial & Localized Application Scenarios

From fine chemical plants in North America to synthesis facilities across the EU and East Asia, discover how Methyl 3-Oxo-2-Phenylbutyrate functions across multiple synthesis streams.

Asymmetric Chiral Synthesis

Employed in multi-step stereoselective synthesis protocols where the α-phenyl ketoester backbone undergoes chiral catalytic hydrogenation, affording enantiomerically pure beta-hydroxy esters for targeted therapeutic research.

Heterocyclic Intermediate Production

Functions as a bi-functional nucleophile/electrophile pair in condensation cascades with amidines, diamines, and hydrazines to assemble complex nitrogenous heterocycles and specialty dye precursors.

Specialty Flavor & Fragrance Scaffolds

Modified derivatives and selectively hydrolyzed analogues form structural core motifs used in aromatic profiling, synthetic musk research, and proprietary fragrance fixation matrices within industrial consumer chemistry.

Technology Roadmap: Continuous Flow & Green Catalysis

The manufacturing paradigm for Methyl 3-Oxo-2-Phenylbutyrate is undergoing a significant transition from traditional batch vessels toward continuous tubular microreactors and biocatalysis.

Microchannel Flow Synthesis

Microreactors replace batch condensation vessels, achieving precise heat transfer, eliminating localized hotspots, and drastically minimizing byproduct formation like phenylacetic condensation oligomers.

Biocatalytic Enantiopurity

Integration of recombinant ketoreductases (KREDs) during pilot synthesis phases enables stereoselective reduction of the keto group directly in aqueous phases with >99.5% enantiomeric excess (ee).

Solvent Recovery & Zero-Waste

Closed-loop rotary distillation and vacuum solvent stripping recover >92% of non-polar process solvents, aligning bulk production pipelines with European REACH and EcoVadis sustainability parameters.

Automated Quality Assays

Online Raman and NIR spectroscopy integration within distillation lines allows real-time quantification of purity, reducing QC quarantine cycles from 72 hours down to immediate release.

China Factory Supply Chain: Resilience, Scalability & Logistics

Leveraging China's comprehensive upstream petrochemical base, dedicated fine-chemical clusters, and advanced transport links to deliver verified reliability for overseas purchasers.

Raw Material Integration

Facilities based in chemical industrial corridors (Hebei, Shandong, Jiangsu) possess domestic access to toluene, benzyl chloride, and acetate precursors, insulating production costs from international shipping spikes.

Tiered Metric Scalability

Synthesizers offer versatile operational scaling, supporting orders ranging from 100g research pilot packs to multi-ton bulk shipments packaged in UN-certified fluorinated HDPE drums and ISO tank containers.

Air & Sea Dangerous Goods Clearance

Decades of chemical logistics management ensure fully compliant Class 9/Dangerous Goods (DG) declarations, verified SDS (Safety Data Sheets in 16 languages), and frictionless customs documentation through major global hubs.

Localized Support & International Compliance Safeguards

Purchasing fine chemical intermediates across borders requires ironclad compliance, legal clarity, and transparent laboratory verification.

End-User Declarations (EUD)

We provide vetted legal documentation assistance, ensuring customers easily compile end-use statements that satisfy national boards, pharmaceutical inspectorates, and destination customs officials.

Independent 3rd Party Verification

In addition to our factory in-house GC-MS testing, blind samples from each batch are deposited with certified third-party analytical laboratories (SGS, Eurofins, or national institutes) for neutral verification.

24/7 Multilingual Procurement Desk

Our dedicated regulatory and technical desk operates across European (CET), American (EST), and Asian (CST) business hours, resolving import compliance, tracking inquiries, and tender submissions promptly.

Technical & Commercial Procurement FAQ

In-depth responses to the most critical technical, analytical, regulatory, and supply questions raised by chemical engineers and procurement directors.

What is the standard purity threshold and primary isomer profile of your supply?
Our industrial-scale Methyl 3-Oxo-2-Phenylbutyrate is manufactured to a verified assay specification of ≥99.0% by Gas Chromatography (FID) and HPLC. Tautomeric keto-enol equilibrium dynamics are documented within the Certificate of Analysis (COA) to ensure that customers running NMR or IR characterization recognize equilibrium shifts caused by polar solvents without mistaking them for chemical impurities.
How does the facility prevent oxidation or ester degradation during maritime transit?
The keto-ester scaffold can undergo trace decarboxylative degradation or photo-oxidation if exposed to thermal stress and atmospheric air. We package the liquid material under a high-purity dry nitrogen blanket in amber fluorinated drums or sealed steel canisters lined with epoxy-phenolic coatings, accompanied by moisture desiccant bags and temperature-logging monitors upon request.
What regulatory credentials are required to import this chemical compound?
Because Methyl 3-oxo-2-phenylbutyrate is monitored internationally under specific precursor regulatory frameworks (such as UN INCB guidelines and national chemical diversion rules), purchasers must be registered business entities possessing appropriate commercial research licenses, university accreditation, or industrial precursor usage permits along with a signed End-User Declaration.
Can you accommodate custom synthesis, ester variations, or deuterated standards?
Yes. Our R&D technical synthesis team handles requests for homologues including Ethyl 3-oxo-2-phenylbutyrate, ring-halogenated aryl variants, and isotopically labeled reference standards (e.g., d3-methyl derivatives) for analytical bio-quantification and pharmacokinetic internal calibration studies.
What payment, lead-time, and Incoterms structures are standard for overseas contracts?
Typical Incoterms include FOB Tianjin/Shanghai, CIF destination hub, or DDP via dedicated logistics forwarders where permissible. Standard stock orders are dispatched within 48 to 72 hours following documentary clearance, with flexible institutional payment modalities including wire transfer (T/T), confirmed Letter of Credit (L/C) for multi-ton contracts, and escrow arrangements.
Are samples available for pilot evaluation prior to high-volume commitments?
Yes, qualification sample kits (typically 50g, 100g, or 500g) are supplied complete with comprehensive analytical dossiers containing GC-FID chromatograms, H-NMR spectra, Karl Fischer titration results, and Safety Data Sheets (SDS) to allow qualified lab QA/QC teams to conduct independent testing.

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