质量
tested for UHPLC-MS
保质期
limited shelf life, expiry date on the label
包含
0.095-0.105 % (v/v) trifluoroacetic acid (T)
杂质
≤0.0001% non-volatile
≤0.5 ppb fluorescence (quinine) at 365 nm
≤0.7 ppb fluorescence (quinine) at 254 nm
≤50 ppb UHPLC-MS (q-TOF) (Reserpin, ESI(+))
透射比
230 nm, ≥35%
254 nm, ≥90%
痕量阳离子
Ca: ≤0.25 mg/kg
K: ≤0.25 mg/kg
Mg: ≤0.25 mg/kg
Na: ≤1 mg/kg
UHPLC-梯度
≤30 mAU at 254 nm (drift)
≤4 mAU at 254 nm (peak)
适用性
passes test for UHPLC-MS
InChI
1S/CH4O/c1-2/h2H,1H3
InChI key
OKKJLVBELUTLKV-UHFFFAOYSA-N
正在寻找类似产品? 访问 产品对比指南
应用
Mixture of methanol with 0.1% trifluoroacetic acid and water with 0.1% trifluoroacetic acid was used as the mobile phase in the HPLC apparatus, used for the quantification of eight quinolones (danofloxacin, oxolinic acid, flumequine, enrofloxacin, ciprofloxacin, sarafloxacin, difloxacin and marbofloxacin) in bovine muscle, milk and aquacultured products.
警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1
储存分类代码
3 - Flammable liquids
WGK
WGK 1
法规信息
新产品
此项目有
Validation of a liquid chromatography-tandem mass spectrometric method for the quantification of eight quinolones in bovine muscle, milk and aquacultured products.
Van Hoof N
Analytica Chimica Acta, 529 (1), 265-272 (2005)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持