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Good Quality Dipotassium EDTA White Crystal Powder Blood Sampling Additive
US$1.50
25 kg
Sample price:US$40.00/kg.Request sample
Product profile
Customization
AvailableCAS No.
25102-12-9Formula
C10h17kn2o8Model NO.
EDTA K2EINECS
217-895-0Classification
High Purity MaterialGrade
ARSpecific Usage
For Biological Purpose, Blood Collection AnticoagulantContent
>99%Usage
Laboratory Reagents, Analytical Reagents, Diagnostic ReagentsSource
Dry PowderHabit Appellation
EDTA K2Application
Scientific Research, Health, Blood Sampling ExaminationProperty
Additives for Blood CollectionColor
White Crystal PowderTaste
OdorlessMolecular Weight
404.6Water Solubility
More Than 60%Density
1.767-1.8 at 20℃pH Value
3.8 to 5.8,5% Aqueous Solution, G/MlPurity
Above 99%Transport Package
CartonSpecification
500g/bottleTrademark
DeShengOrigin
Ezhou City, Hubei Province, ChinaProduction Capacity
5 Tons Per MonthKey features
High Purity Grade: AR grade with purity above 99%, suitable for precise laboratory and diagnostic applications.
Superior Solubility: Potassium salt offers better solubility in blood than sodium salt, preventing sample dilution.
Stable Blood Morphology: Has minimal effect on blood cell morphology, ensuring accurate routine blood testing results.
Standard Anticoagulant: Internationally recommended for vacuum blood collection tubes, especially purple cap tubes.
Versatile Applications: Suitable for blood routine, glycated hemoglobin, and blood type identification tests.
Customizable Packaging: Available in 25kg or 20kg barrels, with OEM/ODM services and sample-based customization.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples CertifiedExport Year: 7 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤6.73h
AI-Powered supplier vetting
SummaryThe supplier is a combined manufacturing and trading enterprise with chemical, synthetic-material, medical-device, and related product activities. It reports two production lines, specified annual capacities for several products, finished-product inspection instructions, inventory capability, and an off-peak lead time within 15 working days. Service processes for corrective and preventive actions and customer complaints are documented and followed. R&D personnel provide technical support, with design and verification records available for audit, but no SDK is available. The supplier provides OEM services for well-known brands and can customize from samples. Limitations include no valid manufacturing-capacity contract with related subcontractors, no overseas warehouse, showroom, agent, or branch, and no stated overseas service countries. No explicit certification holdings or customer case details are provided.
Supplier typeThe supplier’s stated scope covers manufacturing of basic chemical raw materials, synthetic and bio-based materials, special chemical products, sealing fillers, engineering plastics, and Category I and Category II medical-device sales. It is identified as a combined company rather than an offshore company, indicating a mixed manufacturing and commercial operating model.
After-Sales capabilityThe supplier has documented and followed procedures for corrective and preventive actions and customer complaints, and technology engineers provide technical support for production and after-sales service. However, it reports no overseas agents or branches, no overseas warehouse or showroom, and zero stated countries for overseas services, limiting evidence of local international support.
R&D capabilityR&D engineers are responsible for R&D and technical support, and relevant design input, output, review, verification, and validation documents are available for audit. The supplier reports software-instrument capability using MestReNova, but no SDK is available, so the evidence supports established R&D activity rather than full software-development integration capability.
Production capacityThe supplier operates two production lines and reports defined annual capacities, including 600 tons of serum separation gel, 500 tons of tris base, 30 tons of dipotassium ethylenediaminetetraacetate, 20 tons of tripotassium EDTA, and 0.6 tons of lithium heparin. It also reports inventory capability, standardized finished-product inspection instructions, and an off-peak lead time within 15 working days; however, it lacks a valid manufacturing-capacity contract with related subcontractors.
Customization capabilityThe supplier explicitly offers design customization from samples and reports OEM services for well-known brands. Its quality-control information also states that own-brand product quality-control capability is present, although the specific designation is recorded as “DS.”
Product Q&A
Q:Who is the manufacturer?
A:
We are Hubei Xindesheng Material Technology Co., Ltd., a professional manufacturer of in vitro diagnostic reagent raw materials.
Q:Where is the company located?
A:
Huarong District, Ezhou City, Hubei Province, is adjacent to Wuhan City. Welcome to visit the company!
Q:What is the delivery time?
A:
It is determined based on the inventory status of the product and the production and delivery status on that day. Generally, if there is stock available, shipment will be arranged on the day of placing the order.
Q:How to choose the transportation method?
A:
Determine based on the urgency of the customer's purchase of products and needs. When the quantity of products is low and the value is high, it is recommended to choose air freight or international express delivery; When there is a large quantity of products, choosing sea or land transportation is more cost-effective.
Q:What are the payment methods available?
A:
T/T, LC, etc
Send Inquiry
*To:
Hubei New Desheng Material Technology Co., Ltd
Hubei New Desheng Material Technology Co., Ltd*Content:
Supplier replies will be sent to your registered email
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