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Merck

576794

Ammonium-14N chloride

99.99 atom % 14N, 15N-depleted, 99% (CP)

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About This Item

Formule linéaire :
14NH4Cl
Poids moléculaire :
53.49
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
235-186-4

Nom du produit

Ammonium-14N chloride, 99.99 atom % 14N, 15N-depleted, 99% (CP)

InChI key

NLXLAEXVIDQMFP-QMVMUTFZSA-N

InChI

1S/ClH.H3N/h1H;1H3/i;1+0

SMILES string

[14NH4+].[Cl-]

isotopic purity

99.99 atom % 14N

assay

99% (CP)

form

solid

mp

340 °C (subl.) (lit.)

mass shift

depleted

Catégories apparentées

Application

- Nitrogen cycling studies in Environmental research
- agricultural fertilizer efficiency assessment
- Protein turnover investigations in biological systems
- Chlorination reaction mechanism studies

Features and Benefits

Features
  • Cost-effective solution for Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP) applications.
  • High purity of Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP) ensures optimal performance.
  • Exceptional stability and compatibility with various ingredients.
  • Versatile use in different formulations involving Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP).


Benefits
  • Increases market competitiveness of products containing Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP).
  • Reduces time to market for products utilizing Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP).
  • Improves overall product quality and consumer satisfaction.
  • Enhances product efficacy and reliability in formulations.

General description

Ammonium-14N chloride 99.99 atom % 14N, 15N-depleted, 99% (CP) is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.

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.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Classe de stockage

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Consulter la Bibliothèque de documents

Cyrill A Rentsch et al.
European urology, 66(4), 677-688 (2014-03-29)
Whether the commonly used bacillus Calmette-Guérin (BCG) strains Connaught and Tice confer different treatment responses in non-muscle-invasive bladder cancer (NMIBC) is unknown. To compare clinical efficacy, immunogenicity, and genetics of BCG Connaught and Tice. A prospective randomized single-institution trial with
Christine Burkard et al.
PloS one, 9(7), e101762-e101762 (2014-07-16)
Studies of viral entry into host cells often rely on the detection of post-entry parameters, such as viral replication or the expression of a reporter gene, rather than on measuring entry per se. The lack of assays to easily detect
Allison L Boyd et al.
The Journal of experimental medicine, 211(10), 1925-1935 (2014-09-03)
Allogeneic hematopoietic stem cell (HSC) transplantation (HSCT) is currently the leading strategy to manage acute myeloid leukemia (AML). However, treatment-related morbidity limits the patient generalizability of HSCT use, and the survival of leukemic stem cells (LSCs) within protective areas of
Sewa Rijal et al.
Blood, 125(18), 2815-2824 (2015-03-05)
Phosphoinositide signaling regulates diverse cellular functions. Phosphoinositide-3 kinase (PI3K) generates PtdIns(3,4,5)P3 and PtdIns(3,4)P2, leading to the activation of proliferative and anti-apoptotic signaling pathways. Termination of phosphoinositide signaling requires hydrolysis of inositol ring phosphate groups through the actions of PtdIns(3,4,5)P3 3-phosphatase
Jackie Perrin et al.
Journal of cell science, 128(13), 2269-2277 (2015-05-23)
TM9 family proteins (also named Phg1 proteins) have been previously shown to control cell adhesion by determining the cell surface localization of adhesion proteins such as the Dictyostelium SibA protein. Here, we show that the glycine-rich transmembrane domain (TMD) of

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