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Merck

57619

乙酸 – 三乙胺溶液 1:1

suitable for HPLC, 2M:2M aqueous solution, LiChropur

同義詞:

三乙基乙酸铵 溶液, 三乙胺:乙酸 1:1 溶液

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線性公式:
CH3COOH · N(CH2CH3)3
CAS 編號:
分子量::
161.24
Beilstein:
3688333
MDL號碼:
分類程式碼代碼:
51242002
NACRES:
NA.21

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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

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本產品
9364574558849540
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

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產品號碼
描述
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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


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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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