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485306

Sigma-Aldrich

Ammonium-14N2 sulfate solution

40 wt. % in H2O, 99.99 atom % 14N

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About This Item

Linear Formula:
(14NH4)2SO4/H2O soln.
CAS Number:
Molecular Weight:
132.13
EC Number:
MDL number:
UNSPSC Code:
12352314
PubChem Substance ID:

description

15N-depleted

isotopic purity

99.99 atom % 14N

form

solid

concentration

40 wt. % in H2O

refractive index

n20/D 1.396

density

1.23 g/mL at 25 °C

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


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

485306-VAR:
485306-BULK:
485306-1KG:


Certificates of Analysis (COA)

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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
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)
Adam Kawałek et al.
Aging, 5(1), 67-83 (2013-02-22)
We studied the role of peroxisomal catalase in chronological aging of the yeastHansenula polymorpha in relation to various growth substrates. Catalase-deficient (cat) cells showed a similar chronological life span (CLS) relative to the wild-type control upon growth on carbon and
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

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