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Merck
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Key Documents

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319740

Sigma-Aldrich

2-Nitrofuran

97%

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About This Item

Fórmula empírica (Notação de Hill):
C4H3NO3
Número CAS:
609-39-2
Peso molecular:
113.07
Número MDL:
MFCD00013442
Código UNSPSC:
12352100
ID de substância PubChem:
24859185
NACRES:
NA.22

Ensaio

97%

forma

crystals

pb

84 °C/13 mmHg (lit.)

pf

29-33 °C (lit.)

cadeia de caracteres SMILES

[O-][N+](=O)c1ccco1

InChI

1S/C4H3NO3/c6-5(7)4-2-1-3-8-4/h1-3H

chave InChI

FUBFWTUFPGFHOJ-UHFFFAOYSA-N

Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Flam. Sol. 1

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

190.4 °F - closed cup

Ponto de fulgor (°C)

88 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Liyun Liu et al.
Frontiers in cellular and infection microbiology, 8, 233-233 (2018-07-28)
Objectives:Citrobacter freundii is a frequent cause of nosocomial infections and a known cause of diarrheal infections, and has increasingly become multidrug resistant (MDR). In this study, we aimed to determine the genetic diversity, the antimicrobial resistance profiles and in vitro
Jinyan Gong et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1146, 122018-122018 (2020-04-26)
This study established a validated analytical method for the first time on the determination of nitrofuran metabolites, including semicarbazide (SEM), 1-aminohydantoin (AHD), 3-amino-2-oxazolidinone (AOZ) and 3-amino-5-morpholinomethyl-2-oxazolinone (AMOZ) in gelatin Chinese medicine. A C18 column with the mobile phase consisting of
Hui Li et al.
Xenobiotica; the fate of foreign compounds in biological systems, 47(2), 103-111 (2016-04-20)
1. Nitrofurantoin (NFT), a 5-nitrofuran derivative, has been widely used for the treatment of specific urinary tract infections. It has been reported that exposure to NFT was associated with various adverse effects, particularly hepatotoxicity and pneumotoxicity. The objective of the study
Brian T Veach et al.
Journal of AOAC International, 101(3), 897-904 (2017-12-01)
This paper describes a rapid and robust method utilizing a single liquid-liquid extraction for the quantitation and confirmation of chloramphenicol, florfenicol, and nitrofuran metabolites in honey. This methodology combines two previous extraction methods into a single extraction procedure and utilizes
Pierre Guichard et al.
Food chemistry, 342, 128389-128389 (2020-12-04)
LC-MS/MS method for confirmation of nitrofuran metabolites in meat and aquaculture products, including the nifursol metabolite (DNSH), was developed. The nitrofuran metabolites investigated were as follows: 3-amino-2-oxazolidinone (AOZ), 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ), 1-aminohydantoine (AHD), semicarbazide (SEM) and 3,5-dinitrosalicylic acid hydrazide (DNSH). The
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