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C7165

Sigma-Aldrich

Citrate-phosphate-dextrose solution

aseptically filled

Synonym(s):

Citrate-phosphate-glucose

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About This Item

UNSPSC Code:
12161700
NACRES:
NA.25

sterility

aseptically filled

Quality Level

form

liquid

pH

5.2-5.8

storage temp.

2-8°C

General description

Citrate-phosphate-dextrose solution (CPD) is an anticoagulant solution. It has 15% less citrate ion over citrate-phosphate-dextrose solution with adenine (ACD) and provides improved isotonicity, oxygen release function and posttransfusion viability for red blood cells.

Application

Citrate-phosphate-dextrose solution has been used as an anti-coagulant in bovine blood. It has also been used in the storage of fluorescein isothiocyanate (FITC) labeled erythrocytes. Citrate-phosphate-dextrose solution is suitable for erythrocyte survival studies and whole blood storage.

Other Notes

Suggested anticoagulant: whole blood ratio: 1:14

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Citrate phosphate dextrose (CPD) anticoagulant in blood transfusion
McCullough J and Weiblen BJ
Minnesota Medicine, 56(11), 980-982 (1973)
C1-inhibitor reduces hepatic leukocyte-endothelial interaction and the expression of VCAM-1 in LPS-induced sepsis in the rat
Croner RS, et al.
Microvascular Research, 67(2), 182-191 (2004)
Mònica Arman et al.
Malaria journal, 7, 243-243 (2008-11-26)
Platelet-mediated clumping of Plasmodium falciparum-infected erythrocytes (IE) is a parasite adhesion phenotype that has been associated with severe malaria in some, but not all, field isolate studies. A variety of experimental conditions have been used to study clumping in vitro
Real-time feedback of histotripsy thrombolysis using bubble-induced color Doppler
Zhang X, et al.
Ultrasound in Medicine & Biology, 41(5), 1386-1401 (2015)
Alexander P Duryea et al.
IEEE transactions on ultrasonics, ferroelectrics, and frequency control, 62(12), 2068-2078 (2015-12-17)
Remanent bubble nuclei generated by primary cavitation collapse can limit the efficiency of histotripsy softtissue fractionation. When these residual bubbles persist from one histotripsy pulse to the next, they can seed the repetitive nucleation of cavitation bubbles at a discrete

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