Skip to Content
Merck

E8008

Ethylenediaminetetraacetic acid solution

0.02% in DPBS (0.5 mM), sterile-filtered, BioReagent, suitable for cell culture

Synonym(s):

EDTA solution

Sign In to View Organizational & Contract Pricing.

Select a Size

Pricing and availability is not currently available.

About This Item

Empirical Formula (Hill Notation):
C10H16N2O8
CAS Number:
Molecular Weight:
292.24
NACRES:
NA.75
PubChem Substance ID:
eCl@ss:
39030907
UNSPSC Code:
12352204
MDL number:
Beilstein/REAXYS Number:
1716295

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Ethylenediaminetetraacetic acid solution, 0.02% in DPBS (0.5 mM), sterile-filtered, BioReagent, suitable for cell culture

InChI

1S/C10H16N2O8/c13-7(14)3-11(4-8(15)16)1-2-12(5-9(17)18)6-10(19)20/h1-6H2,(H,13,14)(H,15,16)(H,17,18)(H,19,20)

SMILES string

OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CC(O)=O

InChI key

KCXVZYZYPLLWCC-UHFFFAOYSA-N

sterility

sterile-filtered

product line

BioReagent

form

solution

concentration

0.02% in DPBS (0.5 mM)

technique(s)

cell culture | mammalian: suitable

impurities

endotoxin, tested

pH

7.1-7.7

shipped in

wet ice

storage temp.

2-8°C

Quality Level

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
EDS43178803620
technique(s)

cell culture | mammalian: suitable

technique(s)

-

technique(s)

electrophoresis: suitable

technique(s)

-

product line

BioReagent

product line

BioUltra

product line

-

product line

-

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

200

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

-

pH

7.1-7.7

pH

2.5 (23 °C, 10 g/L)

pH

-

pH

-

impurities

endotoxin, tested

impurities

-

impurities

-

impurities

-

Application

Ethylenediaminetetraacetic acid solution has been used to remove confluent cell monolayers in swine testicular (ST-cells) culture.[1] It has also been used to detach embryonic stem cells (ESCs) from matrigel[2] and primary human fibroblasts.[3]

General description

Ethylenediaminetetraacetic acid (EDTA) is an aminopolycarboxylic acid and a hexadentate ligand. It chelates with metal ions to form an octahedral complex especially with cations.[4] Ethylenediaminetetraacetic acid (EDTA) is an anticoagulant, which prevents clotting of blood. It is implicated in platelet aggregation in pseudothrombocytopenia.[5] EDTA chelates with calcium and is effective in solubilisation of the atheromatous plaques.[6] Calcium disodium EDTA administration is effective in slowing down the progression of chronic kidney disease.[7] It is a chelator used to remove calcium from cell washing and suspension media. EDTA reduces cell clumping.[8]

Physical form

Solution in Dulbecco′s phosphate buffered saline without calcium and magnesium

related product

Product No.
Description
Pricing

Storage Class

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Exosomes from embryonic mesenchymal stem cells alleviate osteoarthritis through balancing synthesis and degradation of cartilage extracellular matrix
Wang Y, et al.
Stem Cell Research & Therapy, 8(1), 189-189 (2017)
The genotoxicity of physiological concentrations of chromium (Cr (III) and Cr (VI)) and cobalt (Co (II)): an in vitro study
Figgitt M, et al.
Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis, 688(1-2), 53-61 (2010)
Ex vivo Lung bioengineering
Lung Stem Cells in the Epithelium and Vasculature, 151-151 (2015)
EDTA chelation therapy for cardiovascular disease: a systematic review
Seely DMR, et al.
BMC Cardiovascular Disorders, 5(1), 32-32 (2005)
Environmental fate and microbial degradation of aminopolycarboxylic acids
Bucheli-Witschel M and Egli T
FEMS Microbiology Reviews, 25(1), 69-106 (2001)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service