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159034

Sigma-Aldrich

Acetohydroxamic acid

98%

Sinonimo/i:

AHA

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5 G
CHF 60.20
10 G
CHF 90.70
50 G
CHF 394.00

About This Item

Formula condensata:
CH3CONHOH
Numero CAS:
Peso molecolare:
75.07
Beilstein:
1739019
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

CHF 60.20


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Livello qualitativo

Saggio

98%

Punto di fusione

88-90 °C (lit.)

Gruppo funzionale

amine

Stringa SMILE

CC(NO)=O

InChI

1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4)
RRUDCFGSUDOHDG-UHFFFAOYSA-N

Informazioni sul gene

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Descrizione generale

Acetohydroxamic acid is a potent inhibitor of bacterial urease activity and reduces urinary ammonia levels.[1] 2-Acetohydroxamic acid loaded floating microspheres forms an efficient drug delivery system for the treatment of Helicobacter pylori.[2]

Applicazioni

Acetohydroxamic acid was used:
  • to study the mechanism of complexation of iron (III) with acetohydroxamic acid[3]
  • to study the inhibitory mechanism of lansoprazole and omeprazole on Helicobacter pyloni[4]
  • in urease inhibition studies[5][6]
  • for in situ generation of nitrosocarbonylmethane as a Diels-Alder dienophile[7]
Used in urease inhibition studies[5][6] and for in situ generation of nitrosocarbonylmethane as a Diels-Alder dienophile.[7]

Pittogrammi

Health hazard

Avvertenze

Danger

Indicazioni di pericolo

Consigli di prudenza

Classi di pericolo

Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Dispositivi di protezione individuale

Eyeshields, Gloves, type P2 (EN 143) respirator cartridges


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Slide 1 of 3

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Journal of the Chemical Society. Perkin Transactions 1, 1001-1001 (1991)
K Nagata et al.
Antimicrobial agents and chemotherapy, 37(4), 769-774 (1993-04-01)
The gastric proton pump inhibitor lansoprazole, its active analog AG-2000, and omeprazole dose dependently inhibited urease activity extracted with distilled water from Helicobacter pylori cells; the 50% inhibitory concentrations were between 3.6 and 9.5 microM, which were more potent than
D P Griffith et al.
The Journal of urology, 140(2), 318-324 (1988-08-01)
Acetohydroxamic acid is known to inhibit bacterial urease activity, thus, reducing urinary ammonia levels. A double-blind placebo-controlled clinical trial of acetohydroxamic acid was conducted at 12 Veterans Administration spinal cord injury units. A total of 210 male spinal cord injury
Mechanism of iron (III) complex formation. Activation volumes for the complexation of the iron (III) ion with thiocyanate ion and acetohydroxamic acid.
Funahashi S, et al.
Inorganic Chemistry, 22(14), 2070-2073 (1983)
R B Umamaheshwari et al.
The Journal of pharmacy and pharmacology, 55(12), 1607-1613 (2004-01-24)
This investigation is part of our ongoing effort to develop effective drug delivery systems for the treatment of Helicobacter pylori infection using polycarbonate (PC) floating microspheres as drug carriers. In an effort to augment the anti-H. pylori effect of acetohydroxamic

Questions

  1. Hello, Could you tell me the percentage of impurities and define specifically which impurities we can find in this reagent ? Thank you,

    1 answer
    1. The product impurities are not identified or quantified. Please see the Specification Sheet: https://www.sigmaaldrich.com/specification-sheets/360/076/159034-BULK_______ALDRICH__.pdf

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