Eucalyptus Oil

Eucalyptus Oil

Product Name: Eucalyptus Leaf Oil
English name: Eucalyptus oil
Appearance: Colorless, clear, oily liquid
Extraction method: Distillation extraction
Aroma type: with a unique odor of eucalyptus leaves
Scope of application: cosmetics, massage, aromatherapy, health products, daily chemical products
Usage: If the concentration of a single essential oil is high, it needs to be diluted with base oil
Storage method: sealed, away from light, heat, cool and irritating at room temperature
Shelf life: 24 months
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High-Cineole Eucalyptus Refinement (E. globulus) - Xi'an Tihealth

Through engineered fractional steam distillation, Xi'an Tihealth provides a clinical-grade Eucalyptus Essential Oil optimized for peak bioactivity. By precisely regulating the thermal gradient during extraction from fresh Eucalyptus globulus leaves, we stabilize the 1,8-Cineole (Eucalyptol) fraction at ≥70% or ≥80% as per bespoke industrial requirements. This technical precision ensures the oil maintains its full range of volatile monoterpenes while satisfying the stringent purity criteria of international pharmacopoeias (USP, BP, EP).

Operating as a performance-driven B2B supplier, our facility ensures every industrial batch exhibits a distinctive, crisp camphorous organoleptic profile with zero synthetic adulterants. Our technical isolation process is complemented by nitrogen-shrouded processing, making this essential oil a premier active ingredient for mucolytic pharmaceutical excipients, dermaceutical antiseptics, and high-performance oral hygiene systems.

 

Analytical Parameters

 

Analytical Dimension

B2B Technical Standard

Validation Protocol

Refractive Index (nD20)

1.4580 – 1.4700

ISO 280

Active Biomarker

1,8-Cineole (Eucalyptol) ≥ 70.0% / 80.0%

GC-MS / HPLC

Optical Rotation (alphaD20)

0° to +10°

Polarimetry

Specific Gravity (d2020)

0.9000 – 0.9250

Electronic Density Meter

Phytochemical Origin

100% Eucalyptus globulus (Australian Provenance)

Botanical DNA Audit

Miscibility

Fully soluble in 5 parts 70% (v/v) ethanol.

ISO Standard 856

 

Operational Excellence

Performance Metric Tihealth Proprietary Standard Supply Chain Impact
Distillation Integrity Fractional Heat Regulation < 0.3°C Retention of 95%+ heat-sensitive cineole fractions.
Safety Dossier Full Compliance with BP/USP/ISO 3515 Zero rejection rate in pharmaceutical procurement.
Traceability Matrix QR-Coded Batch Fingerprinting Instant technical verification for QA departments.

 

Industrial Utility

Eucalyptus Oil Industrial Utility
Clinical & Industrial Integration

1. Pharmaceutical Excipients: Acts as a natural mucolytic support in bronchial inhalants and enteric-coated formulations.

2. Periodontal Bioactives: Critical antimicrobial component in high-potency antiseptic mouthwashes and gum-care systems.

3. Dermaceutical Topicals: Facilitates skin penetration for localized analgesic and anti-inflammatory formulations.

4. Biosanitization: Natural, eco-friendly active for clinical-grade surface disinfectants (verified 90%+ microbial inhibition).

 

Strategic Partnership & OEM

Integrated Contract Manufacturing Solutions

Xi'an Tihealth functions as a Strategic Manufacturing Partner for international health brands, offering:

  • Chemotype Calibration: Customizing Cineole ratios (70%-85%) to target specific bio-efficacy.
  • Documentary Support: Rapid provision of MSDS, TDS, and SGS certificates for global filings.
  • Scalable Industrial Hub: Monthly raw material reserves > 50 Tons for seamless high-volume supply.
  • Quality Assurance: Continuous GC-MS monitoring during automated filling cycles.
Xi'an Tihealth Industrial Hub

 

 
Cargo Integrity & Logistics
 
Packaging design for liquid products
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Global Distribution
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Payment Methods
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Trade Aspect Governance & Support
Packaging Matrix SS316 Stainless Steel (180kg) or HDPE industrial barrels. All units are nitrogen-flushed to halt oxidation.
Payment Protocols Irrevocable L/C at sight, T/T (Bank Transfer), and verified digital sample transactions.
Logistics Compliance Specialized Hazardous Goods Management (UN-standard labeling). Supports DDP/CIF "Dual-Clearing" solutions.

 

Eucalyptus-Specific FAQ

Why is the Cineole content in your oil higher than the market average?

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Standard commercial grades often stabilize at 60%. Our Fractional Distillation selectively captures the cineole-rich heart of the run, ensuring a consistent purity ≥ 70%-80% for clinical applications.

Is your oil verified for pharmaceutical-grade purity (BP/USP)?

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Yes. Our refining process targets the removal of undesired aldehydes and moisture, fulfilling the analytical standards of British and US Pharmacopoeias for therapeutic use.

How do you prevent the oxidation of the 1,8-Cineole during cross-border transit?

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We employ nitrogen-blanketing within airtight SS316 industrial containers. This creates an oxygen-free environment, effectively preserving the chemical integrity for up to 24 months.

Do you provide Pre-Shipment Samples (PSS) for bulk validation?

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Certainly. We provide 10-50ml Pre-Shipment Samples. We also facilitate third-party audits (e.g., SGS) to ensure batch consistency before container dispatch.

What is the flash point of your standardized eucalyptus oil for sea freight?

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Typical flash point is ~49°C. As a responsible supplier, we handle all logistics according to IMDG (International Maritime Dangerous Goods) regulations to ensure safe delivery.

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