V800457
Oxalic acid
≥98%, crystalline, Vetec™, LR grade
Synonym(s):
Ethanedioic acid
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
HO2CCO2H
CAS Number:
Molecular Weight:
90.03
UNSPSC Code:
12352300
PubChem Substance ID:
EC Number:
205-634-3
Beilstein/REAXYS Number:
385686
MDL number:
Assay:
≥98%
Form:
crystalline
Grade:
LR
Product Name
Oxalic acid, LR, ≥98%
grade
LR
vapor density
4.4 (vs air)
vapor pressure
<0.01 mmHg ( 20 °C)
product line
Vetec™
assay
≥98%
form
crystalline
mp
189.5 °C (dec.) (lit.)
solubility
water: soluble 108 g/L at 25 °C
density
1.9 g/cm3 at 25 °C
functional group
carboxylic acid
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
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Still not finding the right product?
Explore all of our products under Oxalic acid
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 1
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| V800457-500G | 04061833001059 |