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Merck

586765

Aniline-4-13C

99 atom % 13C

Sinónimos:

Benzenamine-4-13C

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Fórmula lineal:
13CC5H4NH2
Número CAS:
55147-71-2
Peso molecular:
93.11
UNSPSC Code:
12352005
PubChem Substance ID:
329758443
MDL number:
MFCD01075584
Isotopic purity:
99 atom % 13C
Mass shift:
M+1

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InChI

1S/C6H7N/c7-6-4-2-1-3-5-6/h1-5H,7H2/i1+1

SMILES string

Nc1cc[13cH]cc1

InChI key

PAYRUJLWNCNPSJ-OUBTZVSYSA-N

isotopic purity

99 atom % 13C

bp

184 °C (lit.)

mp

-6 °C (lit.)

density

1.033 g/mL at 25 °C

mass shift

M+1

storage temp.

2-8°C

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General description

Aniline-4-13C 99 atom % 13C 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.

Application

- High-resolution NMR spectroscopy
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- reaction mechanism investigations

Features and Benefits

Features
  • Cutting-edge technology in production.
  • Comprehensive support and documentation provided.
  • Flexible ordering options for different scales.
  • Expert technical assistance available.


Benefits
  • Streamlines the synthesis of complex molecules.
  • Supports innovative approaches in organic chemistry.
  • Enhances the efficiency of chemical reactions.
  • Facilitates the development of new therapeutic agents.

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.

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2 - Resp. Sens. 1

Clase de almacenamiento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

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Ronald Besandre et al.
Organic letters, 15(7), 1666-1669 (2013-03-15)
N-substituted indoles are synthesized from primary amines through a tandem reaction sequence. Initial condensation of the amine with an α-(o-haloaryl)ketone or aldehyde is followed by intramolecular aryl amination catalyzed by CuI. A variety of anilines and alkyl amines, including those
Laya Siroos Rezaei et al.
Environmental technology, 33(19-21), 2273-2280 (2013-02-12)
Aerobic granules can be formed in sequencing batch airlift reactors (SBAR) and sequencing batch reactors (SBR). Comparing these two systems, the SBAR has excellent mixing condition, but due to a high height-to-diameter ratio (H/D), there is no performance capability at
Timo Stahl et al.
Journal of the American Chemical Society, 135(4), 1248-1251 (2013-01-15)
Heterolytic splitting of the Si-H bond mediated by a Ru-S bond forms a sulfur-stabilized silicon cation that is sufficiently electrophilic to abstract fluoride from CF(3) groups attached to selected anilines. The ability of the Ru-H complex, generated in the cooperative
Chia-Chi Su et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 48(9), 1012-1018 (2013-04-12)
This study was undertaken to investigate the feasibility of applying the Fered-Fenton process to the degradation of m-phenylenediamine, by examining the effect of varying the initial H2O2 and Fe(2+) concentrations, the initial pH and electric current on the process efficiency.
Regina Mažeikienė et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 106, 34-40 (2013-01-30)
For the first time, chemical oxidation of aniline and N-methylaniline with dichromate as oxidant has been studied by Raman spectroscopy with 785 nm laser beam excitation, and the suitability of this technique for kinetic study of this process was demonstrated.
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