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Good Quality Heparin Sodium 9041-08-1 External Anticoagulant
US$1.50
25 kg
Sample price:US$20.00/gram.Request sample
Product profile
Customization
AvailableCAS No.
9041-08-1Formula
(C12h16ns2na3)20Model NO.
Heparin SodiumEINECS
232-681-7Classification
Biochemical ReagentsGrade
ARSpecific Usage
For Biological Purpose, For Tissue Medium Purpose, Technical Grade, Pratical Use, Pro Analysis, Blood AnticoagulantContent
Purity Above 99%Usage
Laboratory Reagents, Diagnostic ReagentsSource
Dry PowderHabit Appellation
Heparin SodiumApplication
Scientific Research, HealthProperty
Biochemical ReagentColour
WhiteStorage Conditions
Room TempForm
PowderWater Solubility
SolubleOEM Packing
YesValid Period
3 YearsPotency
Over 150iu/MgpH Value
5.0-7.5Clarity of Solution
Colorless ClarificationTransport Package
CartonSpecification
10g/bottle, 20g/bottle, 50g/bottleTrademark
DeShengOrigin
Ezhou City, Hubei Province, ChinaProduction Capacity
20 Kg Per MonthKey features
High Purity Grade: Purity above 99% with AR grade standard for biological purposes.
Effective Anticoagulant: Prevents platelet aggregation and inhibits fibrinogen transformation.
Multiple Packaging Options: Available in 10g, 20g, and 50g bottles packed in cartons.
Long Valid Period: Shelf life of 3 years when stored at room temperature.
Customization Available: OEM and ODM services available with customization from samples.
High Potency: Potency exceeds 150 IU/mg for superior performance.
Water Soluble: Easily soluble in water with colorless clarification.
Manufacturer Direct: Produced by Hubei New Desheng with professional R&D team.
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: ≤10.35h
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:What is the purity and potency of this product?
A:
The product has a purity above 99% and a potency of over 150IU/mg.
Q:How should Heparin Sodium be stored?
A:
It should be stored at room temperature and has a validity period of 3 years.
Q:What are the available packaging sizes?
A:
We offer 10g/bottle, 20g/bottle, and 50g/bottle options, packed in cartons.
Q:Is OEM customization available for this product?
A:
Yes, OEM service is available, including customization from samples.
Q:What are the payment terms accepted?
A:
We accept LC, T/T, PayPal, Western Union, and small-amount payments.
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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