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Merck

68487

Oxalic acid concentrate

0.1 M (COOH)2 (0.2N), eluent concentrate for IC

Synonym(s):

Oxalic acid solution

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About This Item

Linear Formula:
HOOCCOOH
CAS Number:
Molecular Weight:
90.03
NACRES:
NB.21
PubChem Substance ID:
UNSPSC Code:
12161700
MDL number:
Concentration:
0.1 M (COOH)2 (0.2N)
Form:
liquid
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Quality Level

form

liquid

concentration

0.1 M (COOH)2 (0.2N)

technique(s)

ion chromatography: suitable

SMILES string

OC(=O)C(O)=O

InChI

1S/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)

InChI key

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Application

Metrohm IC application note AN-C-139: Cations andamines in the water-steam cycle.

Metrohm IC application note AN-C-138: Zinc,nickel, calcium, and magnesium in borated water of a pressurized water reactor(PWR).

Metrohm IC application note AN-C-113:Determination of lysine and standard cations in a lysine sample.

Other Notes

Visit the IC Portal to learn more


Storage Class

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves



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L K Massey et al.
Journal of agricultural and food chemistry, 49(9), 4262-4266 (2001-09-18)
Consumption of soybeans and food products made from them is increasing because of their desirable nutritional value. However, the oxalate content of seeds from 11 cultivars of soybean showed relatively high levels of total oxalate from 0.67 to 3.5 g/100
R de Water et al.
American journal of kidney diseases : the official journal of the National Kidney Foundation, 33(4), 761-771 (1999-04-09)
Urinary calcium oxalate (CaOx) crystals and crystal agglomerates are normally harmlessly excreted, but in nephrolithiasis they are retained by tubular epithelial cells and shifted into the renal interstitium. This crystalline material induces an inflammatory response consisting of an increase in
G M Gadd
Advances in microbial physiology, 41, 47-92 (1999-09-29)
The production of organic acids by fungi has profound implications for metal speciation, physiology and biogeochemical cycles. Biosynthesis of oxalic acid from glucose occurs by hydrolysis of oxaloacetate to oxalate and acetate catalysed by cytosolic oxaloacetase, whereas on citric acid