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Lithium Heparin Analysis of Pure Grade Blood Sampling Additive
US$1.50
25 kg
Sample price:US$20.00/gram.Request sample

Product profile

Customization

Available

CAS No.

9045-22-1

Formula

N.a.

Model NO.

Lithium Heparin

EINECS

686-293-1

Color

White

Appearance

Powder

Storage Conditions

Room Temp

Form

Powder

Water Solubility

Soluble

Purity

Above 99%

Primitive Trait

White Amorphous Powder

Performance

Odorless, Soluble in Water, Easily Hygroscopic

Potency

Greater Than 150iu/Mg

Anhydrous Potency

Greater Than 160iu/Mg

Average Molecular Weight

15000

Valid Period

3 Years

Purity Above

99%

Aqueous Solution

Sealed Storage at 0-4 Degrees Celsius

Transport Package

Carton

Specification

10g/bottle, 20g/bottle, 50g/bottle

Trademark

DeSheng

Origin

Ezhou City, Hubei Province, China

Production Capacity

20 Kg Per Month

Key features

High Purity Grade: Purity above 99% with potency greater than 150iu/Mg.
Effective Anticoagulant: Used as external anticoagulant for blood sampling with high correlation to serum.
Stable Chemical Properties: Lithium is more stable than sodium, combining slower with PLTs.
Water Soluble: Easily soluble in water with 125 mg/mL solubility.
Long Valid Period: Valid for 3 years when stored at room temperature.
Customization Available: Customization from samples and OEM/ODM services offered.
Manufacturer Direct: Produced by Hubei New Desheng with professional R&D team.
Fast Lead Time: Peak and off-peak season lead time within 15 workdays.

Company profile

Hubei New Desheng Material Technology Co., Ltd
Importers and ExportersPatents AwardedExhibition Experience
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: ≤6.78h

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 of the Lithium Heparin?
A:
The purity is above 99% with a potency greater than 150iu/Mg.
Q:How should the product be stored?
A:
Store at room temperature. Aqueous solution requires sealed storage at 0-4 degrees Celsius.
Q:What is the main use of this product?
A:
It is used as an external anticoagulant for blood sampling.
Q:Is customization available for this product?
A:
Yes, customization from samples is available, along with OEM and ODM services.
Q:What is the lead time for orders?
A:
The lead time is within 15 workdays for both peak and off-peak seasons.

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