Industrial Chemical Whitepaper & Global Dossier

High-Quality Cas 315-37-7 Supplier & Factory

Technical synthesis parameters, ultra-pure chromatographic validation, and global commercial supply chain execution for institutional research and pharmaceutical intermediates procurement.

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Executive Chemical Profile: CAS 315-37-7 Structure & Specifications

CAS 315-37-7, chemically recognized as Testosterone 17β-heptanoate (Testosterone Enanthate), represents an esterified steroid intermediate of paramount significance in biochemical research, pharmaceutical standard development, and industrial steroid synthesis.

≥99.2%
Batch HPLC Purity
<0.1%
Single Max Impurity
16+
Years In-House Synthesis
100%
Batch HPLC/MS Audit
Analytical Parameter Documented Specification Range Observed Factory Release Value Validation Instrument
Chemical Name Testosterone 17β-heptanoate / Testosterone Enanthate Confirmed Identity 1H-NMR / FTIR Spectrum
CAS Registry Number 315-37-7 Verified CAS Identification CAS Inventory Registry
Molecular Formula & Weight C26H40O3 — 400.59 g/mol 400.60 g/mol ±0.1 High-Res Mass Spectrometry (HRMS)
Chromatographic Purity (HPLC) ≥98.00% (USP / EP Reference Standard Grade) 99.35% – 99.70% Reverse-Phase HPLC-UV (240 nm)
Melting Point Range 34.0 °C to 39.0 °C 36.5 °C – 37.8 °C Automated Melting Point Apparatus
Specific Optical Rotation [α]D +77.0° to +82.0° (in dioxane) +79.5° Digital Polarimeter (Sodium D-line)
Loss on Drying (Moisture) ≤ 0.50% 0.18% Karl Fischer Titration
Residual Solvents Meets ICH Q3C Guidelines (Ethanol, Hexane, DCM) Complies with Class 2/3 limits Headspace GC-FID

Macro Industry Landscape: Commercial Sourcing Bottlenecks & Solutions

A rigorous examination of supply continuity, intermediate pricing pressures, and analytical qualification criteria shaping international fine chemical supply chains.

Traceability & Identity Integrity

Global steroid hormone precursors face pervasive risks of mislabeling and polymorphic variance. Miaoou enforces end-to-end analytical identity checking, establishing that every kilogram of CAS 315-37-7 matches its raw spectral blueprint before downstream export authorization.

Upstream Intermediate Volatility

Supply shocks in phytosterol fermentation intermediates (4-AD and ADD) frequently disrupt commercial ester production. Our integrated raw materials stocking model maintains 6-month buffer inventories, protecting international buyers from price spikes and shipment stalls.

Customs Clearance Architecture

Complex classification codes across tariff regions frequently delay chemical imports. We formulate proactive HS-Code classifications, bilingual export declarations, and verified SDS data sheets matching European, American, and Asia-Pacific regional customs requirements.

Industrial Synthesis Chemistry & Technical Manufacturing Roadmap

The catalytic esterification of testosterone requires precise thermal moderation, inert atmosphere control, and multi-stage solvent purification to avert related substance impurities.

STAGE 01

Sterol Bio-Oxidation

Soybean phytosterols undergo multi-stage microbial bioconversion to generate 4-androstene-3,17-dione (4-AD), followed by chemoselective reduction into high-purity testosterone base material.

STAGE 02

Catalytic Esterification

Testosterone is reacted with heptanoic anhydride or heptanoyl chloride in an anhydrous pyridine/DMAP catalytic matrix, controlling the 17β-hydroxy esterification equilibrium while suppressing secondary side-chain modifications.

STAGE 03

Impurity Scavenging

Acidic washes, microfiltration, and specialized silica-gel chromatographic filtration strip out residual heptanoic acid, unreacted steroid base, and trace metal catalysts below detectable pharmacopeial thresholds.

STAGE 04

Recrystallization & Micronization

Controlled cooling recrystallization in food-grade organic solvent matrices produces uniform, crystalline white powders. Material is lyophilized/vacuum-dried to guarantee loss-on-drying parameters <0.2%.

Localized Support & Cross-Border Compliance Assurance

Supplying biological institutions and fine chemical buyers across North America, Europe, and Asia requires granular adherence to local chemical import regulations.

European Union (REACH)

Our regulatory team validates export documentation aligned with EU REACH criteria, non-restricted chemical inventories, and specialized CLP regulation (EC 1272/2008) safety protocols.

North American Compliance

Shipments to qualified institutional research laboratories are paired with GHS-compliant 16-section SDS data sheets, TSCA non-commercial R&D statements, and full customs proforma invoicing.

Double-Vacuum Packaging

Because CAS 315-37-7 exhibits a low melting threshold (34–39 °C), bulk packaging utilizes multi-layer pharmaceutical-grade foil vacuum bags with desiccants and temperature-buffered packaging for tropical routes.

Independent Third-Party Auditing

Beyond our in-house ISO 9001 certified labs, we welcome blind testing via third-party ISO 17025 accredited laboratories (e.g., SGS, Intertek, Janoshik) to ensure complete procurement confidence.

Institutional & Industrial Application Scenarios

Exploring the core analytical, pharmacological, and commercial domains requiring pharmaceutical-grade CAS 315-37-7 material.

Reference Standard Benchmarking

Analytical testing labs and university biochemistry departments utilize high-purity CAS 315-37-7 as a primary analytical calibrant for high-performance liquid chromatography (HPLC) and gas chromatography-mass spectrometry (GC-MS) assay quantifications.

Endocrine & Androgen Receptor Assays

In vitro hormone receptor binding affinity studies examine testosterone ester hydrolysis kinetics, cellular proliferation pathways, and lipid solubility dynamics across comparative vertebrate models.

Formulation & Emulsion Stability Research

Contract research organizations (CROs) evaluate oil carrier miscibility (sesame, castor, ethyl oleate), benzyl alcohol/benzyl benzoate preservative equilibria, and thermal crystallization profiles across storage conditions.

Forward-Looking Roadmap: Green Chemistry & Continuous Flow Esterification

The manufacturing paradigm for steroid hormone intermediates is transitioning from legacy batch reaction vessels toward continuous flow synthesis and bio-catalysis.

Microreactor Continuous Flow

Deploying microfluidic continuous flow chemical reactors enables millisecond temperature control during heptanoyl acylation. This innovation eliminates local thermal hotspots, slashing related substance impurities by 65% compared to legacy batch reactors.

Enzymatic Biocatalytic Acylation

Developing immobilized lipase enzymes (such as Candida antarctica lipase B) to selectively esterify the C-17 position eliminates hazardous acid chlorides and corrosive organic bases, yielding a completely eco-neutral, heavy-metal-free production stream.

Blockchain Traceability & Digital COA

Integrating cryptographic batch verification links every drum of CAS 315-37-7 to an immutable digital certificate containing raw NMR spectra, HPLC trace files, and timestamped export declaration stamps to eradicate gray-market counterfeiting.

Frequently Asked Questions: CAS 315-37-7 Procurement

Clear, direct responses addressing analytical documentation, minimum orders, storage protocols, and regulatory compliance.

What is the typical HPLC purity profile of your factory batches?

Every commercial batch produced at Hebei Miaoou Technology Co., Ltd. satisfies a minimum release target of ≥98.0%, with standard lots achieving 99.2% to 99.7% chromatographic purity. Individual related substance impurities are restricted to <0.1% per ICH Q3A guidelines.

Which analytical test reports accompany each shipment?

Shipments include an authentic batch-specific Certificate of Analysis (COA) containing the exact lot number, analytical HPLC chromatograms, Fourier-Transform Infrared (FTIR) spectral identity validation, melting point ranges, Karl Fischer water titration, and residual solvent quantification.

How does the low melting point of CAS 315-37-7 affect shipping and storage?

With a melting range between 34.0 °C and 39.0 °C, CAS 315-37-7 can aggregate or melt if exposed to prolonged summer heat in transit. We package the material in heavy-duty, double-vacuum aluminum foil enclosures alongside thermal barrier padding, recommending long-term storage in cool, desiccated conditions between 2 °C and 8 °C.

Are these chemical materials intended for human or veterinary administration?

No. Materials cataloged on this website are distributed exclusively for qualified institutional laboratory research, synthesis benchmarking, and chemical intermediate manufacturing. They are not intended, formulated, or authorized for human or direct veterinary clinical use.

Can you accommodate custom packaging scales for institutional buyers?

Yes. We support custom packaging options ranging from 100g sample containers for QC testing and characterization up to 1kg, 5kg, and 25kg multi-layer pharmaceutical-grade polyethylene-lined fiber drums for high-volume manufacturing requirements.

What is the standard inquiry response timeline for international buyers?

Our dedicated export and regulatory compliance division provides official quotes, product dossiers, and sample COAs within 24 hours of receipt on regular business days.

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Connect Directly with Our Fine Chemical Synthesis Engineers

Whether you require pilot-scale validation quantities or bulk industrial supply contracts, our technical export team delivers rapid quote generation, analytical data packs, and international trade compliance assistance within 24 hours.