Is the product suitable for medical device applications?

Yes, it is widely used in the medical device industry for blood testing and analysis.

What is the molecular formula of EDTA K3?

The molecular formula is C10H17K3N2O10.

EDTA K3 Tripotassium Ethylenediaminetetraacetate Acid for Vacutainer

Name: EDTA K3 Tripotassium Ethylenediaminetetraacetate Acid for Vacutainer
Brand: Hubei New Desheng Material Technology Co., Ltd
SKU: 2062985735

Hubei, ChinaHubei New Desheng Material Technology Co., Ltd

US$1.50

25 kg

Product specifications

500g

Sample price:US$40.00/kg.Request sample

Product profile

Customization

Available

CAS No.

65501-24-8T65501-24-8

Formula

C10h17K3n2o10

Model NO.

EDTA K3

Carboxyl No.

Dicarboxylic Acid

Alkyl No.

Unsaturated Acid

Appearance

Powder

Source

Hydrolysis

Colour

White

Product Name

EDTA K3

Usage

Blood Collection Tube Additives

Function

Blood Anti-Coagulant

Industry

Medical Device

Application

Blood Testing & Analysis

Transport Package

500g/Bottle

Specification

Purity-99.5%

Trademark

DESHENG

Origin

Ezhou, China

HS Code

2921219000

Production Capacity

1000kgs/Month

Key features

Blood Anti-Coagulant Function: Tripotassium EDTA used as anticoagulant in vacuum blood collection tubes for blood cell analysis.

High Purity Grade: High-purity tripotassium ethylenediaminetetraacetate suitable for medical device applications.

Manufacturer Direct Supply: Produced by Hubei Xindesheng Material Co., Ltd., a professional biochemical reagent manufacturer.

OEM and ODM Services: Customization from samples available with dedicated R&D engineers and production lines.

Stable Sales Record: Products have stable sales at home and abroad since 2005 with excellent quality.

Versatile Chelating Agent: Forms stable complexes with alkali metals, rare earth elements, and transition metals.

Fast Lead Time: Average lead time within 15 workdays for both peak and off-peak seasons.

Comprehensive Product Line: Includes EDTA K2, K3, Na2, heparin, and other blood collection tube additives.

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: ≤11.59h

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.”