HomeProductsBuilding BlocksFunctional GroupsCarboxylic AcidsOxamic acid
Chemical structure of CAS 471-47-6

Oxamic acid

In Stock•Starting at $9 for 1 g•Purity ≥ 97%
CAS No.471-47-6
MDL No.MFCD00008006
MFC2H3NO3
MW89.05
InChI KeySOWBFZRMHSNYGE-UHFFFAOYSA-N
CUSTOM SYNTHESISPRECLINICAL SUPPORT

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
1 g97%+$9In Stock
5 g97%+$17In Stock
10 g97%+$28In Stock
25 g97%+$57In Stock
50 g97%+$106In Stock
100 g97%+$203In Stock
250 g97%+$500In Stock
500 g97%+$958In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

Oxamic acid is a dicarboxylic acid monoamide formed by the formal condensation of one carboxy group of oxalic acid with ammonia. It functions as an Escherichia coli metabolite and is the conjugate acid of an oxamate.

CAS No.471-47-6
Product NameOxamic acid
IrritantIrritant
Signal Word:Warning
HCode:H315-H319-H335
PCode:P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Repair and mutagenic potential of oxaluric acid, a major product of singlet oxygen-mediated oxidation of 8-oxo-7,8-dihydroguanine.

Chemical research in toxicology • Vol. 14, Issue 1 • 2001
PMID: 11170507DOI: 10.1021/tx0001629

Structural basis for altered activity of M- and H-isozyme forms of human lactate dehydrogenase.

Proteins • Vol. 43, Issue 2 • 2001
PMID: 11276087DOI: 10.1002/1097-0134(20010501)43:2<175::aid-prot1029>3.0.co;2-#

Hypersensitization of tumor cells to glycolytic inhibitors.

Biochemistry • Vol. 40, Issue 18 • 2001
PMID: 11331019DOI: 10.1021/bi002426w

Further studies on the effects of topical lactate on amino acid efflux from the ischemic rat cortex.

Brain research • Vol. 901, Issue 1-2 • 2001
PMID: 11368947DOI: 10.1016/s0006-8993(01)02183-7

Documentation

Similar Products