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Merck

01-4600

Sigma-Aldrich

柠檬酸铵 二元

suitable for atomic absorption spectrometry, 98.0-102.0%

别名:

枸椽酸氢二铵, 柠檬酸 铵盐, 柠檬酸氢二铵

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About This Item

线性分子式:
HOC(CO2H)(CH2CO2NH4)2
CAS号:
分子量:
226.18
Beilstein:
4925760
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

蒸汽密度

1.8 (vs air)

化驗

98.0-102.0%

形狀

solid

存貨情形

available only in Japan

pH值

5.2 (20 °C, 50 g/L)

適合性

suitable for atomic absorption spectrometry

SMILES 字串

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 密鑰

YXVFQADLFFNVDS-UHFFFAOYSA-N

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象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Lorina Gjonaj et al.
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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
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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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