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Merck
CN

604003

Sigma-Aldrich

Acetanilide-(ring-13C6, carbonyl-13C)

99 atom % 13C

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About This Item

Linear Formula:
CH313CONH13C6H5
CAS Number:
Molecular Weight:
142.11
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
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isotopic purity

99 atom % 13C

form

solid

bp

304 °C (lit.)

mp

113-115 °C (lit.)

density

1.283 g/mL at 25 °C

mass shift

M+7

SMILES string

C[13C](=O)N[13c]1[13cH][13cH][13cH][13cH][13cH]1

InChI

1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)/i2+1,3+1,4+1,5+1,6+1,7+1,8+1

InChI key

FZERHIULMFGESH-NWWRDLAKSA-N

Application

- High-resolution NMR spectroscopy
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- Environmental monitoring applications

Features and Benefits

Features
  • High isotopic purity for reliable synthesis.
  • Stable isotopic composition for consistent results.
  • Versatile applications across various therapeutic areas.
  • Compatibility with multiple diagnostic platforms.


Benefits
  • Enhances the accuracy and reliability of metabolic studies.
  • Increases efficiency in the drug developmentpipeline.
  • Supports compliance with regulatory standards.
  • Provides a competitive advantage in the pharmaceutical market.

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

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

321.8 °F - closed cup

Flash Point(C)

161.00 °C - closed cup


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Shalini Jayasundera et al.
Journal of agricultural and food chemistry, 51(13), 3829-3835 (2003-06-12)
The dynamics of acetanilide pesticide interactions with organic matter (OM) surrogates were examined using nuclear magnetic resonance (NMR) spectroscopy. Differences in the relative changes in (13)C and (1)H spin-lattice relaxation times (T(1)) were measured at multiple molecular sites of metolachlor

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