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Supelco

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
MDL number:
UNSPSC Code:
12161700
PubChem Substance ID:
NACRES:
NB.21

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

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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.

Linkage

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related product

Product No.
Description
Pricing

Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), 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
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
A Amoroso et al.
Journal of the American Society of Nephrology : JASN, 12(10), 2072-2079 (2001-09-20)
Primary hyperoxaluria type 1 (PH1) is an autosomal recessive disorder that is caused by a deficiency of alanine: glyoxylate aminotransferase (AGT), which is encoded by a single copy gene (AGXT). Molecular diagnosis was used in conjunction with clinical, biochemical, and
R Shapiro et al.
Transplantation, 72(3), 428-432 (2001-08-15)
The appropriate use of liver transplantation in children with type-1 primary hyperoxaluria (PH-1) is not well established. We reviewed our experience with 36 children with PH-1, including 12 who underwent liver transplantation. From 1989-1998, 36 children from 10 families in
Y Nakagawa et al.
The Journal of clinical investigation, 76(4), 1455-1462 (1985-10-01)
One reason that some people are prone to calcium oxalate nephrolithiasis is that they produce urine that is subnormal in its ability to inhibit the growth of calcium oxalate crystals. We have identified in human urine a glycoprotein (GCI) that

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