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Aminomalonic acid (CAS 1068-84-4)

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Alternate Names:
2-Aminopropanedioic Acid
CAS Number:
1068-84-4
Purity:
≥97%
Molecular Weight:
119.08
Molecular Formula:
C3H5NO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Aminomalonic acid, derived from malonic acid, holds importance as a component in the synthesis of diverse compounds. With its versatility, aminomalonic acid serves as a valuable starting material for the production of carboxylic acids, amines, and other compounds. Furthermore, aminomalonic acid acts as an intermediate in the synthesis of vitamins and other important compounds. Its utility extends to the study of compound effects on various cell cultures, as well as investigating the impact of drugs on cellular systems.


Aminomalonic acid (CAS 1068-84-4) References

  1. Enzymatic formation of aminomalonic acid from ketomalonic acid.  |  NAGAYAMA, H., et al. 1958. Nature. 181: 417-8. PMID: 13504217
  2. Detection and possible origins of aminomalonic acid in protein hydrolysates.  |  Copley, SD., et al. 1992. Anal Biochem. 201: 152-7. PMID: 1621954
  3. Micellization of true amphoteric surfactants.  |  Li, Y., et al. 2013. J Colloid Interface Sci. 411: 47-52. PMID: 24112839
  4. Application of Metabolic Profiling to Abdominal Aortic Aneurysm Research.  |  Qureshi, MI., et al. 2017. J Proteome Res. 16: 2325-2332. PMID: 28287739
  5. Plasma metabolic profiling on postoperative colorectal cancer patients with different traditional Chinese medicine syndromes.  |  Hu, XQ., et al. 2018. Complement Ther Med. 36: 14-19. PMID: 29458921
  6. Urinary biomarker panel for diagnosing patients with depression and anxiety disorders.  |  Chen, JJ., et al. 2018. Transl Psychiatry. 8: 192. PMID: 30232320
  7. GC/MS-based metabolomics strategy to analyze the effect of exercise intervention in diabetic rats.  |  Jing, L. and Chengji, W. 2019. Endocr Connect. 8: 654-660. PMID: 31042671
  8. Plasma Metabolomics Reveals Diagnostic Biomarkers and Risk Factors for Esophageal Squamous Cell Carcinoma.  |  Yu, M., et al. 2022. Front Oncol. 12: 829350. PMID: 35198450
  9. Aminomalonic acid and its congeners as potential in vivo inhibitors of L-asparagine synthetase.  |  Milman, HA., et al. 1979. Enzyme. 24: 36-47. PMID: 35346
  10. The effect of tacrolimus-induced toxicity on metabolic profiling in target tissues of mice.  |  Xie, D., et al. 2022. BMC Pharmacol Toxicol. 23: 87. PMID: 36443830
  11. Aminomalonic acid. Spontaneous decarboxylation and reaction with 5-deoxypyridoxal.  |  Thanassi, JW. 1970. Biochemistry. 9: 525-32. PMID: 5415959
  12. Quantitative analysis and comparative decarboxylation of aminomalonic acid, beta-carboxyaspartic acid, and gamma-carboxyglutamic acid.  |  Hauschka, PV., et al. 1980. Anal Biochem. 108: 57-63. PMID: 7457858
  13. Hydroxamate derivatives of substrate-analogous peptides containing aminomalonic acid are potent inhibitors of matrix metalloproteinases.  |  Krumme, D., et al. 1998. FEBS Lett. 436: 209-12. PMID: 9781680

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Aminomalonic acid, 100 mg

sc-357287B
100 mg
$73.00

Aminomalonic acid, 1 g

sc-357287
1 g
$407.00

Aminomalonic acid, 5 g

sc-357287A
5 g
$1417.00

Aminomalonic acid, 10 g

sc-357287C
10 g
$2259.00