Heparin Sodium 9041-08-1 Blood Sampling Additive for Blood Ammonia Determination

Name: Heparin Sodium 9041-08-1 Blood Sampling Additive for Blood Ammonia Determination
Brand: Hubei New Desheng Material Technology Co., Ltd
SKU: 2096625265

Hubei, ChinaHubei New Desheng Material Technology Co., Ltd

US$1.50

25 kg

Sample price:US$20.00/gram.Request sample

Product profile

Customization

Available

CAS No.

9041-08-1

Formula

(C12h16ns2na3)20

Model NO.

Heparin Sodium

EINECS

232-681-7

Classification

Biochemical Reagents

Grade

Specific Usage

For Biological Purpose, For Tissue Medium Purpose, Technical Grade, Pratical Use, Pro Analysis, Blood Anticoagulant

Content

Purity Above 99%

Usage

Laboratory Reagents, Diagnostic Reagents

Source

Dry Powder

Habit Appellation

Heparin Sodium

Application

Scientific Research, Health

Property

Biochemical Reagent

Colour

White

Storage Conditions

Room Temp

Form

Powder

Water Solubility

Soluble

Purity

Above 99%

Valid Period

3 Years

Potency

Over 150iu/Mg

pH Value

5.0-7.5

Clarity of Solution

Colorless Clarification

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 Standard: Purity above 99% with strict quality control and batch consistency.

Flexible Potency Options: Potency ranges from 150IU/mg to 180IU/mg, customizable to needs.

20 Years Experience: Nearly 20 years of technical experience in extraction and purification.

Complete Product System: Covers heparin lithium, EDTA salt, coagulant, and serum separation gel.

Professional Support: Provides professional usage guidance and flexible packaging solutions.

Fast Delivery: Shipment arranged on the day of order if stock is available.

OEM/ODM Service: Customization from samples available for specific requirements.

Versatile Application: Suitable for clinical biochemistry, emergency testing, and skincare.

Company profile

Importers and ExportersPatents AwardedExhibition Experience

Hubei New Desheng Material Technology Co., Ltd

Hubei, China

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: ≤5.18h

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 grade is required for lithium heparin used in blood collection tubes?

The lithium heparin in the blood collection tube requires biochemical grade heparin lithium.

Q:As an additive for common blood routine tubes, what is the recommended dosage of lithium heparin?

The general recommended dosage is 15-25IU per ml of blood, and the recommended dosage is 20IU/ml. The specific usage can be carried out according to the actual situation.

Q:Why do some lithium heparin tubes show tiny coagulation fragments after blood sampling?

This is because the local anticoagulant concentration in the lithium heparin anticoagulant tube is too high, which causes part of the blood to enter the blood collection tube and cannot be fully mixed with the lithium heparin, which results in some small clots. This may be caused by the failure to invert and mix the test tube in time after blood sampling.

Q:Where is the company?

Huarong District, Ezhou City, Hubei Province, is adjacent to Wuhan City.Welcome to visit the company!

Q:What is the delivery time?

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.