形狀
liquid
技術
HPLC: suitable
&lambda ;
neat
紫外吸收
λ: 250 nm Amax: ≤0.1
λ: 260 nm Amax: ≤0.05
λ: 300 nm Amax: ≤0.01
λ: 500 nm Amax: ≤0.01
SMILES 字串
CC(O)=O.CCN(CC)CC
InChI
1S/C6H15N.C2H4O2/c1-4-7(5-2)6-3;1-2(3)4/h4-6H2,1-3H3;1H3,(H,3,4)
InChI 密鑰
AVBGNFCMKJOFIN-UHFFFAOYSA-N
尋找類似的產品? 前往 產品比較指南
1 of 4
本產品 | 93645 | 745588 | 49540 |
|---|---|---|---|
| technique(s) HPLC: suitable | technique(s) ion pair chromatography: suitable | technique(s) HPLC: suitable | technique(s) ion pair chromatography: suitable |
| form liquid | form liquid | form liquid | form liquid |
| λ neat | λ - | λ - | λ - |
| UV absorption λ: 250 nm Amax: ≤0.1 | UV absorption - | UV absorption - | UV absorption - |
應用
- Direct enantiomeric resolution of betaxolol with application to analysis of pharmaceutical products.: This study presents a method for the direct enantiomeric resolution of betaxolol, where acetic acid and triethylamine are used to facilitate the chiral separation in analytical processes, showcasing its application in pharmaceutical analysis (Hefnawy et al., 2007).
法律資訊
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
相關產品
產品號碼
描述
訂價
訊號詞
Danger
危險分類
Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類(WGK)
WGK 1
Javier Acosta et al.
Frontiers in bioengineering and biotechnology, 8, 593-593 (2020-07-03)
Nucleoside-2'-deoxyribosyl-transferases (NDTs) catalyze a transglycosylation reaction consisting of the exchange of the 2'-deoxyribose moiety between a purine and/or pyrimidine nucleoside and a purine and/or pyrimidine base. Because NDTs are highly specific for 2'-deoxyribonucleosides they generally display poor activity on modified
Fanghua Zhang et al.
Macromolecular bioscience, 20(7), e2000083-e2000083 (2020-06-20)
Affibody-conjugated RALA (affi-RA) are designed for delivering oligomeric 5-fluorodeoxyuridine (FUdR, metabolite of 5-FU) strand to raise the selectivity of 5-fluorouracil (5-FU), decrease its toxicity and improve its suboptimal therapeutic efficacy. The nanodrugs, FUdR@affi-RA, are spontaneously assembled by electrostatic interaction between
Yosuke Taniguchi et al.
Organic & biomolecular chemistry, 18(15), 2845-2851 (2020-04-02)
Expansion of the triplex DNA forming sequence is required in the genomic targeting fields. Basically, triplex DNA is formed by the interaction between the triplex-forming oligonucleotides and homo-purine region with the target duplex DNA. The presence of the base pair
Oleg V Markov et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-17)
Biological activity of antisense oligonucleotides (asON), especially those with a neutral backbone, is often attenuated by poor cellular accumulation. In the present proof-of-concept study, we propose a novel delivery system for asONs which implies the delivery of modified antisense oligonucleotides
Zujun Liang et al.
Dalton transactions (Cambridge, England : 2003), 49(32), 11249-11259 (2020-08-07)
Platinum based anticancer agents are widely applied in clinic and their major target is believed to be DNA. Herein, the interaction of a photoactivatable diazido Pt(iv) anticancer prodrug trans,trans,trans-[Pt(N3)2(OH)2(py)2] (py = pyridine; 1) with a 15-mer single-G-containing oligodeoxynucleotide (ODN I:
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