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901874

Sigma-Aldrich

Ammonium sulfate

anhydrous, Redi-Dri™, ReagentPlus®, ≥99.0%

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Synonym(s):
Mascagnite
Linear Formula:
(NH4)2SO4
CAS Number:
7783-20-2
Molecular Weight:
132.14
MDL number:
MFCD00003391
UNSPSC Code:
12352116
NACRES:
NA.21

grade

anhydrous

Quality Level

200

product line

ReagentPlus®
Redi-Dri™

Assay

≥99.0%

form

powder

pH

5-6 (25 °C, 132 g/L)

mp

>280 °C (dec.) (lit.)

solubility

water: soluble 132 g/L at 20 °C

density

1.77 g/mL at 25 °C (lit.)

cation traces

Fe: ≤10 ppm
Pb: ≤3 ppm
Se: ≤5 ppm

SMILES string

N.N.OS(O)(=O)=O

InChI

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

InChI key

BFNBIHQBYMNNAN-UHFFFAOYSA-N

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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 is reported to enhance the phytotoxicity of several herbicides like glyphosates. It is formed as a co-product during the manufacture of caprolactam, a precursor of nylon.

Redi-Dri™ technology eliminates clumping and the need for complicated procedures to keep your salts free-flowing. Keeping your salts dry helps improve your results by giving accurate measurements and easier-to-handle salts and buffers. Rather than drying your salts in an oven or desiccator or breaking them apart manually, Redi-Dri™ ensures that your salts will remain easy-to-use for months without worrying about anti-caking agents. Even after repeated openings you can be assured that your results are always accurate. Redi-Dri™ saves you time, energy and money by keeping your salts usable for longer!

Application

Ammonium sulfate may be used in methyl cellulose precipitable tannin assay to examine wine tannin in finished wine samples. It may also be 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.

Features and Benefits

  • Increased efficiency – Eliminate time and effort of loosening hardened powders
  • Safety –Avoid risks of using tools of force to break up clumps
  • Economy –Faster preparation and solvation increase productivity and reduce costs
  • Assured quality –Excellent, expert-tested quality with no anti-caking agents
  • Flexible volumes –Available from research amounts to scale-up quantities

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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  1. How does Redi-Dri™ help keep salts and buffers free-flowing?

    Redi-Dri™ products are specially handled and the bottle is specially designed to ensure that the product will remain dry without adding impurities or additives to the product. Ensuring that you receive the highest quality material that is easy to handle.

  2. Are there any special storage conditions that must be maintained?

    No, Redi-Dri™ products can be stored under the same conditions as the equivalent non-Redi-Dri™ products.

  3. How long will material remain free-flowing after it is opened?

    While the exact amount of time your material will remain free-flowing can vary, this largely depends on the ambient storage conditions and how many times it is opened.

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)
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)
Ammonium Compounds.
Weston CW, et al.
Kirk-Othmer Encyclopedia of Chemical Technology (2003)
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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