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HCID 1990Erstellt: 24. Oktober 2026

Acetohydroxamsure

N-HYDROXYACETAMIDE · AHA · Acetylhydroxamic acid · Acetylhydroxylamine · Acetomenadione · N-hydroxyacetimidic acid · T-41B · NSC 5073

https://huagongshe.com/de/chemical/1990

Molekülstruktur von Acetohydroxamsure

Identifikatoren & physikalische Daten

CAS No.546-88-3
SummenformelC2H5NO2
Durchschnittliche Molmasse75,07 g/mol
Monoisotopische Masse75,0320284 g/mol
SMILESCC(=O)NO
InChIKeyRRUDCFGSUDOHDG-UHFFFAOYSA-N
PubChem CID1990
ChEMBLCHEMBL734
ChEBICHEBI:27777
EC No.208-913-8
DTXSIDDTXSID7022546
Lokaler NameAcetohydroxamsure

Chemische & physikalische Eigenschaften

XLogP-1,6
Polarare Oberfläche (TPSA)49,3
H-Brücken-Donoren2
H-Brücken-Akzeptoren2
Frei drehbare Bindungen0
Schwere Atome5
Formalladung0
Komplexität42,9
ArzneimittelPharmaceuticals -> Listed in ZINC15
pH9.39 (aq soln)
SpringerMaterials PropertiesChemical shift
LogP (Verteilungskoeffizient)log Kow= -1.59-0.7
Löslichkeit5.09e+02 g/L<0.2 [ug/mL] (The mean of the results at pH 7.4)Methanol (Sparingly), Water (Sparingly)Soluble in water.
Human DrugsFDA approved drugs -> Active ingredient
DecompositionWhen heated to decomposition it emits toxic fumes of nitroxides.
Schmelzpunkt89-92 °C90.5 °C88-90 °C (lit.)
Physical DescriptionSolid
Dissociation Constants8.7 (at 25 °C)pKa= 8.70
Siedepunkt133.7°C (rough estimate)
Dichte1.2269 (rough estimate)
Brechungsindex1.4264 (estimate)
LagerbedingungenKeep in dark place,Inert atmosphere,Room temperature
AggregatzustandCrystalline Solid
pKa (Säurekonstante)8.70(at 25℃)
FarbeWhite to pale yellow
Merck14,63
BRN1739019
StabilitätMoisture and Temperature Sensitive
InChI1S/C2H5NO2/c1-2(4)3-5/h5H,1H3,(H,3,4)
InChIKeyRRUDCFGSUDOHDG-UHFFFAOYSA-N
SMILESCC(NO)=O
CAS Datenbank546-88-3(CAS DataBase Reference)
NIST chemische InformationenAcetamide,N-hydroxy(546-88-3)
EPA chemische InformationenAcetohydroxamic acid (546-88-3)

Sicherheit & Vorschriften

GHS-EinstufungDangerH360 (96.1%): May damage fertility or the unborn child [Danger Reproductive toxicity]P203, P280, P318, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 51 reports by companies from 9 notifications to the ECHA C&L Inventory.
Regulatorische InformationenHazard Traits - Developmental Toxicity
FDA-AnforderungenManufacturers, packers, and distributors of drug and drug products for human use are responsible for complying with the labeling, certification, and usage requirements as prescribed by the Federal Food, Drug, and Cosmetic Act, as amended (secs 201-902, 52 Stat. 1040 et seq., as amended21 U.S.C. 321-392).
Hazard Classes and CategoriesRepr. 1B (96.1%)
EntsorgungsverfahrenSRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.
WechselwirkungenConcurrent use of alcoholic beverages with acetohydroxamic acid has resulted in a nonpruritic, reddish, macular skin rash about 30 to 45 minutes after ingestion. The rash may be associated with a general feeling of warmth and tingling, and usually disappears spontaneously in 30 to 60 minutes.Acetohydroxamic acid chelates iron and possibly other heavy metals with concurrent oral administrationthis may result in reduced intestinal absorption of bothif iron therapy is indicated, parenteral administration of iron is recommended.In vitro studies indicate that acetohydroxamic acid and methenamine have a synergistic effect in inhibiting increases in pH caused by urease-producing Proteus spp. and that acetohydroxamic acid potentiates the antibacterial effect of methenamine against these bacteria...
Human Toxicity ExcerptsAcetohydroxamic acid was positive for mutagenicity in the Ames test.Acetohydroxamic acid overdose has not been reported. However, if it should occur, concomitant reduction in platelets and/or white blood cells should be anticipatedreticulocyte count is likely to be elevated, and severe hemolysis may occur.
Drug Induced Liver InjuryDrug Induced Liver Injury Rank (DILIrank 2.0)Acetohydroxamic acidAmbiguous-DILI-concern3Warnings & precautionsDOI:10.1016/j.drudis.2016.02.015
Non-Human Toxicity ExcerptsAcetamide, a metabolite or acetohydroxamic acid, has been shown to cause hepatocellular carcinoma in rats when used in very high doses....in long-term studies in rats, large oral dosages (e.g., 4 g/kg daily) of acetamide, a metabolite of acetohydroxamic acid, have been shown to cause hepatocellular carcinoma.Evidence of toxicity did not occur when the drug was administered subcutaneously in mice at a dosage of 500 mg/kg daily for 60-100 dayshowever, evidence of cumulative toxicity, with death occurring at a mean of 21 days, occurred when the drug was administered subcutaneously at a dosage of 1 g/kg daily.
Antidote and Emergency TreatmentTreatment of overdose: Administration should be stopped. There is no known specific antidote for acetohydroxamic acid overdose. Recommended treatment consists of the following: Monitoring - Close monitoring of hematologic statusSpecific Treatment - Symptomatic treatment as necessary. Blood transfusions if required. Dialysis (considered possible but not yet proven).
Non-Human Toxicity ValuesLD50 Mouse ip 2.5 g/kgLD50 Mouse oral 5 g/kgLD50 Rat oral 4.8 g/kg
Wassergefährdungsklasse (WGK)3
UN-Transportnummer3263
Zollcode29225090
RTECS-Nr.AK8157000
R-Sätze (R)61-40
Toxizitätmmo-sat 160 mmol/plate JOPHDQ 3,557,80
GefahrensymboleT
hazard_noteToxic
Sicherheitshinweise (S)53-45-36/37/39-22
VerpackungsgruppeII
Lagerklasse6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
Gefahrstoffdaten546-88-3(Hazardous Substances Data)
GefahrenklasseRepr. 1B

Anwendungen & Verwendung

Beschreibung

Acetohydroxamic acid is a potent, non-competitive and irreversible inhibitor of bacterial urease (Ki≈lO-7M). This enzyme, which is widely distributed in plants and bacteria, but not in mammalian cells, catalyzes the decomposition of urea to ammonia. Elevated urinary ammonia levels can reduce the antibacterial effectiveness of a number of agents. Thus, acetohydroxamic acid is useful as adjunctive therapy to decrease urinary ammonia and alkalinity in patients with chronic urea-splitting urinary infection. Such infections are a leading cause of recurring complications and death in paraplegics.

Verwenden

Acetohydroxamic acid is a potent inhibitor of bacterial urease activity and reduces urinary ammonia levels. 2-Acetohydroxamic acid loaded floating microspheres forms an efficient drug delivery system for the treatment of Helicobacter pylori.Acetohydroxamic acid was used:to study the mechanism of complexation of iron (III) with acetohydroxamic acid.to study the inhibitory mechanism of lansoprazole and omeprazole on Helicobacter pyloni.in urease inhibition studies.for in situ generation of nitrosocarbonylmethane as a Diels-Alder dienophile.Used in urease inhibition studies and for in situ generation of nitrosocarbonylmethane as a Diels-Alder dienophile.