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经验公式(希尔记法):
C13H16N4O6
化学文摘社编号:
分子量:
324.29
UNSPSC Code:
12352200
NACRES:
NA.77
PubChem Substance ID:
EC Number:
205-384-5
Beilstein/REAXYS Number:
8130725
MDL number:
Quality level:
Application
呋喃他酮已被用作液相色谱-质谱(LC-MS/MS)定量测定养殖基质和蜂蜜中硝基呋喃代谢物的参考标准。
Biochem/physiol Actions
硝基呋喃在商业上被用作饲料添加剂,以促进水产养殖、蜂群和牲畜等各个领域的生长。
General description
呋喃他酮是一种含有5-硝基呋喃环的硝基呋喃,是合成抗生素中的一员。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
Nitrofuran antibiotics: a review on the application, prohibition and residual analysis
Vass M, et al.
Veterinary medicine (Auckland, N.Z.), 53(9), 469-469 (2008)
Hiroshige Mikamo et al.
The Japanese journal of antibiotics, 59(6), 468-473 (2007-03-06)
We investigated the efficacies of various administration methods for levofloxacin (LVFX) and tosufloxacin (TFLX) against 161 isolates of Streptococcus pneumoniae and 309 isolates of Haemophilus influenzae isolated in Gifu prefecture, using Monte Carlo simulation. The pharmacokinetic parameters of the fluoroquinolones
Sara Leston et al.
Chemosphere, 82(7), 1010-1016 (2010-11-27)
The use of pharmaceuticals in the food production industry as prophylatic and therapeutic agents is necessary to promote animal health, but may entail significant consequences to natural ecosystems, especially in the cases of overdosing and use of banned pharmaceuticals. The
Zhen-Lin Xu et al.
Talanta, 103, 306-313 (2012-12-04)
A heterologous competitive indirect enzyme-linked immunosorbent assay (ciELISA) for the determination of the furaltadone metabolite 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ) was developed. AMOZ was derivatised with 2-(4-formylphenoxy) acetic acid or 2-(3-formylphenoxy) acetic acid to obtain two novel immunizing haptens. The ability of these
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