7377-03-9
7377-03-9
Chemical Structure
Octanohydroxamic acid
Synonym(s): N-Hydroxyoctanamide; Caprylhydroxamic acid
- CAS 番号: 7377-03-9
- Formula:C8H17NO2
- Molecular Weight:159.23
IUPAC Name: N-hydroxyoctanamide
InChIKey: RGUVUPQQFXCJFC-UHFFFAOYSA-N
SMILES: O=C(CCCCCCC)NO
Biological Activity: Octanohydroxamic acid (N-Hydroxyoctanamide) is a Urease inhibitor. Octanohydroxamic acid acts as a chelating agent that binds to metal cations, thereby assisting in the purification of tin ore. Octanohydroxamic acid is also used as a preservative. Octanohydroxamic acid can be used in research on Escherichia coli infection[1][2][3][4][5].
| 製品番号 | 製品名 | 純度 | 製品説明 | Pricing | |||||||||||||||||||
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Octanohydroxamic acid | 99.86% | Octanohydroxamic acid (N-Hydroxyoctanamide) is a Urease inhibitor. Octanohydroxamic acid acts as a chelating agent that binds to metal cations, thereby assisting in the purification of tin ore. Octanohydroxamic acid is also used as a preservative. Octanohydroxamic acid can be used in research on Escherichia coli infection. | ||||||||||||||||||||
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References
- [1]. Paterson JR. Characterisation of the mode of action of chelating agents against Gram-negative and Gram-positive bacteria (Doctoral dissertation, et al.
- [2]. Lynn L, et al. Antimicrobial, Preservative, and Hazard Assessments from Eight Chemical Classes. ACS omega. 2024 Apr 23;9(16):17869-17877.
- [3]. Evstafeva D, et al. Inhibition of urease-mediated ammonia production by 2-octynohydroxamic acid in hepatic encephalopathy. Nature communications. 2024 Mar 12;15(1):2226.
- [4]. Evstafeva D. Urease inhibitors in the treatment of hepatic encephalopathy (Doctoral dissertation, et al.
- [5]. Liao L, et al. HDAC inhibitor SAHA triggers the production of previously undescribed sesquiterpenes and undergoes biotransformation by the fungus Robillarda sessilis from Verbena officinalis L. Phytochemistry. 2025 May;233:114411.
