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485411

Sigma-Aldrich

Ammonium-14N2 sulfate

99.99 atom % 14N

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About This Item

Linear Formula:
(14NH4)2SO4
CAS Number:
1196157-83-1
Molecular Weight:
132.13
EC Number:
231-984-1
MDL number:
MFCD00167446
UNSPSC Code:
12142200
PubChem Substance ID:
24872071
NACRES:
NA.12

description

15N depleted

isotopic purity

99.99 atom % 14N

form

solid

mp

>280 °C (dec.) (lit.)

application(s)

agriculture

mass shift

depleted

SMILES string

[14NH3].[14NH3].OS(O)(=O)=O

InChI

1S/2H3N.H2O4S/c;;1-5(2,3)4/h2*1H3;(H2,1,2,3,4)/i2*1+0;

InChI key

BFNBIHQBYMNNAN-ONPSQTMSSA-N

Packaging

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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James F Hunter et al.
Environmental science & technology, 48(17), 10227-10234 (2014-08-06)
A large number of organic species emitted into the atmosphere contain cycloalkyl groups. While cyclic species are believed to be important secondary organic aerosol (SOA) precursors, the specific role of cyclic moieties (particularly for species with multiple or fused rings)
Kazunori Sugiura et al.
Biochemical and biophysical research communications, 457(3), 242-248 (2015-01-17)
Intracellular redox state is a critical factor for fundamental cellular functions, including regulation of the activities of various metabolic enzymes as well as ROS production and elimination. Genetically-encoded fluorescent redox sensors, such as roGFP (Hanson, G. T., et al. (2004))
Yohei Y Yamamoto et al.
Journal of molecular biology, 426(14), 2667-2678 (2014-05-27)
Chaperonins are ubiquitous molecular chaperones with the subunit molecular mass of 60kDa. They exist as double-ring oligomers with central cavities. An ATP-dependent conformational change of the cavity induces the folding of an unfolded protein that is captured in the cavity.
Christian Molitor et al.
Planta, 242(3), 519-537 (2015-02-24)
Aurone synthase belongs to the novel group 2 polyphenol oxidases and the presented kinetic characterization suggests a differing aurone biosynthesis in Asteraceae species compared to snapdragon. Aurone synthases (AUS) are polyphenol oxidases (PPO) physiologically involved in the formation of yellow
Houda Banani et al.
International journal of food microbiology, 182-183, 1-8 (2014-05-24)
The yeast-like fungus Aureobasidium pullulans PL5 is a microbial antagonist against postharvest pathogens of fruits. The strain is able to produce hydrolases, including glucanases, chitinases and proteases. The alkaline serine protease gene ALP5 from A. pullulans was cloned, inserted into
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