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608602

Sigma-Aldrich

Ammonium-14N2,sulfate-16O4

99.99 atom % 16O, 99.99 atom % 14N

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About This Item

Formule linéaire :
(14NH4)2S16O4
Poids moléculaire :
132.11
Code UNSPSC :
12352116
ID de substance PubChem :

Description

15N,18O-depleted

Pureté isotopique

99.99 atom % 16O
99.99 atom % 14N

Forme

solid

Pf

>280 °C (dec.) (lit.)

Changement de masse

depleted

Chaîne SMILES 

[14NH3].[14NH3].[16OH]S([16OH])(=[16O])=[16O]

InChI

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

Clé InChI

BFNBIHQBYMNNAN-VNZOPVORSA-N

Conditionnement

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.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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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))
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)
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
Takayoshi Hiyama et al.
The FEBS journal, 281(14), 3113-3125 (2014-05-20)
The last two steps of l-tryptophan (Trp) biosynthesis are catalyzed by Trp synthase, a heterotetramer composed of TrpA and TrpB. TrpB catalyzes the condensation of indole, synthesized by TrpA, and serine to Trp. In the hyperthermophilic archaeon Thermococcus kodakarensis, trpA

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