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Merck
CN

01-4580

Sigma-Aldrich

柠檬酸铵 二元

JIS special grade, ≥99.0%

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别名:
枸椽酸氢二铵, 柠檬酸 铵盐, 柠檬酸氢二铵
线性分子式:
HOC(CO2H)(CH2CO2NH4)2
CAS号:
分子量:
226.18
Beilstein:
4925760
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

等级

JIS special grade

蒸汽密度

1.8 (vs air)

检测方案

≥99.0%

形式

solid

存货情况

available only in Japan

pH值(酸碱度)

5.2 (20 °C, 50 g/L)

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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象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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
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
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
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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