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Merck
CN

V900150

Sigma-Aldrich

柠檬酸铵 二元

98%, Vetec, reagent grade

别名:

枸椽酸氢二铵, 柠檬酸 铵盐, 柠檬酸氢二铵

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关于此项目

线性分子式:
HOC(CO2H)(CH2CO2NH4)2
化学文摘社编号:
分子量:
226.18
Beilstein:
4925760
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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产品名称

柠檬酸铵 二元, Vetec, reagent grade, 98%

等级

reagent grade

蒸汽密度

1.8 (vs air)

产品线

Vetec

方案

98%

SMILES字符串

N.N.OC(=O)CC(O)(CC(O)=O)C(O)=O

InChI

1S/C6H8O7.2H3N/c7-3(8)1-6(13,5(11)12)2-4(9)10;;/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12);2*1H3

InChI key

YXVFQADLFFNVDS-UHFFFAOYSA-N

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法律信息

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Lorina Gjonaj et al.
Organic & biomolecular chemistry, 13(21), 6059-6065 (2015-05-08)
A new method for the selective chemical modification of DNA at cytosine nucleobases using alkoxy- and benzyloxyamines is presented. It is shown that in particular benzyloxyamines are effective DNA modifying agents, giving rise to almost exclusive formation of the mono
S Vollmer et al.
Organic & biomolecular chemistry, 13(20), 5734-5742 (2015-04-23)
Triplexes with a gap in the purine strand have been shown to bind adenosine or guanosine derivatives through a combination of Watson-Crick and Hoogsteen base pairing. Rigidifying the binding site should be advantageous for affinity. Here we report that clamps
Shi-Jun Dong et al.
The international journal of biochemistry & cell biology, 68, 33-41 (2015-08-19)
During the industrial bioethanol fermentation, Saccharomyces cerevisiae cells are often stressed by bacterial contaminants, especially lactic acid bacteria. Generally, lactic acid bacteria contamination can inhibit S. cerevisiae cell growth through secreting lactic acid and competing with yeast cells for micronutrients
Ewa Radzikowska et al.
Organic & biomolecular chemistry, 13(1), 269-276 (2014-11-05)
Chimeric oligonucleotides containing phosphodiester and phosphorothioate linkages have been obtained using the solid phase synthesis. The oligonucleotide parts possessing natural internucleotide phosphate bonds were assembled using commercially available nucleoside 3'-O-(2-cyanoethyl-N,N-diisopropylamino)phosphoramidites 7 whereas the phosphorothioate segment was built using nucleoside 3'-O-(2-thio-1,3,2-oxathiaphospholanes)

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