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Merck
CN

01-4580

Ammonium citrate dibasic

JIS special grade, ≥99.0%

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
EC Number:
221-146-3
UNSPSC Code:
12352100
PubChem Substance ID:
329747289
Beilstein/REAXYS Number:
4925760
MDL number:
MFCD00013068

Key Documents

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InChI key

YXVFQADLFFNVDS-UHFFFAOYSA-N

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

grade

JIS special grade

vapor density

1.8 (vs air)

assay

≥99.0%

form

solid

availability

available only in Japan

pH

5.2 (20 °C, 50 g/L)

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pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
U1528
U2395
U0245
U6170
U0070

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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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