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Merck
CN

V900150

Sigma-Aldrich

Ammonium citrate dibasic

98%, Vetec™, reagent grade

Synonym(s):

Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate

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About This Item

Linear Formula:
HOC(CO2H)(CH2CO2NH4)2
CAS Number:
3012-65-5
Molecular Weight:
226.18
Beilstein:
4925760
EC Number:
221-146-3
MDL number:
MFCD00013068
UNSPSC Code:
12352100
PubChem Substance ID:
329829586

Key Documents

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Product Name

Ammonium citrate dibasic, Vetec™, reagent grade, 98%

grade

reagent grade

vapor density

1.8 (vs air)

product line

Vetec™

Assay

98%

SMILES string

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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Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
WXBD6898V
WXBD6592V
WXBC7605V
WXBC4223V
WXBB1520V

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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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