Products

Featured products

Contact us

WeChat

Hangzhou Yihe Biomedical Technology Co., Ltd.

  • Centella Asiatica Extract CAS 84696-21-9
  • video

Centella Asiatica Extract CAS 84696-21-9

Application:Pharmaceuticals, Cosmetics
  • Yihe Biomedical
  • China


Product Introduction


Centella‍‌‍‍‌‍‌‍‍‌ Asiatica Extract


CAS No.: 84696-21-9


Main Functions

Yihe Biomedical Centella Asiatica Extract is a botanical extract raw material registered under CAS No. 84696-21-9. Available specifications ranges are total glycosides 10%-80%, asiaticoside 10%-90%, madecassoside 10%-90%, and asiatic acid 90%. This product is especially for customers who require different active-component directions for pharmaceutical and cosmetic formulation development.

As per Yihe Biomedical product information Centella Asiatica Extract is principally used for clearing heat and dampness, reducing swelling and detoxifying, activating circulation and also providing anti-inflammatory and analgesic support as well as promoting wound healing. Besides these, it is primarily targeted for skin repair, soothing care and plant-based functional ingredients.Having a definite CAS number and several specifications at hand help pharmaceutical-related clients to choose the suitable grade according to formula target and internal quality requirements.


Application Areas

Centella‍‌‍‍‌‍‌‍‍‌ Asiatica Extract is mainly recognized as a pharmaceutical active substance and as a raw material in cosmetic. It is included in creams, serums, face masks, lotions, and other skincare products that contain naturally derived elements for skin repair and soothing. Different concentration grades make it possible for customers to adjust product positioning, formula composition, and cost management.

In pharmaceuticals, clients may use total glycosides, asiaticoside, madecassoside, or asiatic acid, etc., for their specific fields of research. Yihe Biomedical is ready to provide samples for visual inspection, solubility, compatibility as well as content verification in order to help customers minimize risk at early formulation stage testing.


Company Strengths

Yihe Biomedical incorporates research, production, quality control, and sales. A Hangzhou office and a Nanning factory are its points of operation. The Nanning plant having an area of 3300㎡ was launched in 2019 and is equipped with seven 6-ton extraction tanks, with an annual processing capacity of over 2000 tons of plant raw materials.

Yihe Biomedical regards quality as paramount and implements its Centella Asiatica Extract production method starting at raw material selection and ending with finished-product release. The company uses raw material traceability, incoming inspection, in-process control, finished-product testing, sample retention, and batch traceability. More than 15 key control points are set from feeding, extraction, concentration, drying, blending, and packaging. Finished products must pass both QC testing and QA document review before release. Each batch is assigned a unique batch number and can be traced to raw materials, production line, operator records, testing reports, and logistics information.


Why Choose Us


Pre-Sales‍‌‍‍‌ and After-Sales Support

Pre-Sales Support

1. Prompt Reaction to Queries

We reply to queries within 2 hours and issue first quotes and specs within 24 hours.

2. Sampling Services

We ship you samples for FREE with the Certificate of Analysis (COA) and usage instruction included.

3. Technical Advisory

We help you understand the regulations of your markets (like U.S. Dietary Supplement cGMP, EFSA standards).

4. Custom Sample Production

Perform a small batch trial in a lab based on customer's recipe submission, sample delivery 3–5 business days.

After-Sales Support

1. Use Guidance

Issue technical data sheets (TDS) in detail for product solubility, compatibility & contraindications, recommended dosage, storage conditions, etc.

2. Customer Complaint Management

If there is any problem with the quality, a dedicated team will be formed within 48 hours to offer replacements or refunds for free, and the Quality Director will issue a corrective action report.

3. Sustained Interest in Customer Satisfaction

We take the initiative to contact customers every three months and offer them updated CoAs, literature, and application research materials related to products from the same batch.

4. Stocking Plan for the Long Run

We take responsibility for stocking a safety inventory (≥3 months’ typical usage) of top-selling products to avoid production ‍‌‍‍‌downtime.


FAQ

Q1:‍‌‍‍­ What are your specifications?

A: Specification ranges include total glycosides 10%-80%, asiaticoside 10%-90%, madecassoside 10%-90%, and asiatic acid 90%.

Q2: What is the product CAS number?

A: 84696-21-9.

Q3: What are the main application areas?

A: The most common ones are pharmaceuticals and cosmetics.

Q4: Does Yihe Biomedical offer samples?

A: Yes, we can make samples with a Certificate of Analysis (COA) and some usage information available.

Q5: What is the best way to choose a specification?

A: Specification choice depends on the kind of formula you have, target of active-component, final application, and cost consideration.


Shipping Information

In general, Yihe Biomedical is able to send Centella Asiatica Extract stock specifications within 3 working days of order confirmation. Customized specifications or special processing usually require a production period of 15-25 working days.

Typical stock products come in 25kg/drum packages, and 1kg trial packs are available for use in sample evaluations. In case of large scale or long term orders, it would be advisable to contact Yihe Biomedical for main products safety stock arrangement in order to reduce supply interruption risks and ensure the production ‍‌‍‍‌‍‌‍‍‌stability.‍‌‍‍‌‍‌‍‍‌


CompanyHangzhou Yihe Biomedical Technology Co., Ltd.
Business LayoutHangzhou trade office for international business, customer communication, and logistics coordination; Nanning factory for production and quality control
Factory LocationNanning, Guangxi, close to botanical raw material sources
Factory OperationNanning factory officially started production in 2019
Factory AreaAbout 3,300 m²
Extraction Capacity7 extraction tanks, 6 tons each
Annual Raw Material CapacityOver 2,000 tons of botanical raw materials per year
Product FormsSingle compounds, standardized extracts, ratio extracts, compound granules, and customized grades
Quality DocumentsCOA, TDS, MSDS/SDS, specification sheet; Halal, Kosher, and organic documents available for selected products
Testing CapabilityHPLC, GC/MS, ICP-MS, GC-ECD / GC-MS, headspace gas chromatography, moisture, ash, and particle size testing
Sample SupportSamples can be supplied with sample COA and basic product information
MOQ ReferenceRegular extracts: 25 kg/drum; 1 kg trial pack available; customized products can be discussed from around 5 kg depending on process
Lead Time ReferenceStock products: around 3 working days; customized production: around 15–25 working days
TraceabilityEach batch has a unique batch number linked to raw materials, production records, test reports, and logistics records
Quality ResponseQuality complaints are handled within 48 hours with internal investigation and corrective action when needed


Centella Asiatica Extract


  • Q1: Are you a factory or a trading company?

    We are a professional manufacturer integrating R&D, production, and sales. We control quality directly from the source. You are welcome to visit our factory.
  • Q2: What international certifications do you have?

    Our factory is ISO 9001 certified. Our core products comply with USP/EP standards. For most botanical extracts, we can also provide HALAL and KOSHER certifications.
  • Q3: What is the difference between ratio extracts and standardized extracts?

    Ratio extracts (such as 10:1) mean that 10 kg of raw material is used to produce 1 kg of extract, but the content of active compounds may vary. Standardized extracts, on the other hand, guarantee a specific percentage of active ingredients (such as 5% flavonoids), ensuring consistent efficacy from batch to batch. For pharmaceutical applications, we recommend standardized extracts.
  • Q4: Can you provide a Certificate of Analysis before shipment?

    Of course. Every batch is tested by our in-house quality control laboratory. We provide a detailed Certificate of Analysis (COA), including heavy metals, microbial limits, and active ingredient content. Third-party test reports (such as SGS or Eurofins) can also be provided upon request.
  • Q5: What is your minimum order quantity (MOQ)?

    For high-purity pharmaceutical raw materials, the MOQ is usually [e.g. 25 kg/drum]. For popular botanical extracts, we keep stock available, so sample orders or small trial orders (1–5 kg) are acceptable.
  • Q6: Can these ingredients be legally imported into the USA / EU / Japan?

    Our products comply with most international regulations. Please let us know your target market, and we will provide a regulatory assessment accordingly.
  • Q7: How do you ensure product stability during long-distance sea transportation?

    We use food-grade fiber drums with double-layer sealed inner bags. We can also provide stability data to support your shelf-life claims.

Related Products

Get Quote

top