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Merck

901229

Ammonium sulfate

anhydrous, free-flowing, Redi-Dri™, ACS reagent, ≥99.0%

Synonym(s):

Mascagnite

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About This Item

Linear Formula:
(NH4)2SO4
CAS Number:
7783-20-2
Molecular Weight:
132.14
UNSPSC Code:
12352314
NACRES:
NA.21
EC Number:
231-984-1
MDL number:
MFCD00003391
Assay:
≥99.0%
Grade:
ACS reagent, anhydrous
Form:
powder or crystals
Solubility:
water: soluble 132 g/L at 20 °C

Key Documents

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InChI key

BFNBIHQBYMNNAN-UHFFFAOYSA-N

InChI

1S/2H3N.H2O4S/c;;1-5(2,3)4/h2*1H3;(H2,1,2,3,4)

grade

ACS reagent, anhydrous

product line

Redi-Dri™

assay

≥99.0%

form

powder or crystals

impurities

≤0.005% Insoluble matter

ign. residue

≤0.005%

pH

5.0-6.0 (25 °C, 5%)

mp

>280 °C (dec.) (lit.)

solubility

water: soluble 132 g/L at 20 °C

density

1.77 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤5 ppm, nitrate (NO3-): ≤0.001%, phosphate (PO43-): ≤5 ppm

cation traces

Fe: ≤5 ppm, heavy metals: ≤5 ppm (by ICP-OES)

storage temp.

room temp

Quality Level

100

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General description

Ammonium sulfate is an ammonium salt commonly used as fertilizer. It can be synthesized by neutralizing sulfuric acid with ammonia. It can enhance the phytotoxicity of several herbicides like glyphosates. Ammonium sulfate is formed as a co-product during the manufacture of caprolactam, a precursor of nylon.

Application

Ammonium sulfate was used in methyl cellulose precipitable tannin assay to evaluate wine tannin in finished wine samples. It was also used in making externally mixed aerosols for analyzing the 1 × 3 tandem differential mobility analyzer (1 × 3-TDMA), which is mainly employed for determining the irreversibility of the hygroscopic growth factor of aerosol particles.

Legal Information

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000453688
SLCK9163
SLCG6921
SLCM4188
SLCF5535

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Influence of yeast strain on Shiraz wine quality indicators.
Holt H, et al.
International Journal of Food Microbiology, 165(3), 302-311 (2013)
Industrial catalytic aspects of the synthesis of monomers for nylon production.
Bellussi G and Perego C.
CATTECH, 4(1), 4-16 (2000)
Ammonium Compounds.
Weston CW, et al.
Kirk-Othmer Encyclopedia of Chemical Technology (2003)
The 1-by-3 tandem differential mobility analyzer for measurement of the irreversibility of the hygroscopic growth factor.
Rosenoern T, et al.
Aerosol Science and Technology, 43(7), 641-652 (2009)
Simon Gareth Broadley et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 11), 1450-1459 (2012-10-24)
MshB, a zinc-based deacetylase, catalyses a step in the mycothiol biosynthetic pathway that involves the deacetylation of 1-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-D-myo-inositol (GlcNAc-Ins), via cleavage of an amide bond, to 1-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-D-myo-inositol (GlcN-Ins) and acetate. In this study, MshB was expressed, purified and crystallized. A
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