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线性分子式:
CH313CONH13C6H5
化学文摘社编号:
分子量:
142.11
UNSPSC Code:
12352002
PubChem Substance ID:
MDL number:
产品名称
乙酰苯胺-(环-13C6,羰基-13C), 99 atom % 13C
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
SMILES string
C[13C](=O)N[13c]1[13cH][13cH][13cH][13cH][13cH]1
InChI key
FZERHIULMFGESH-NWWRDLAKSA-N
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
Application
- High-resolution NMR spectroscopy
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- Environmental monitoring applications
- Metabolomic profiling and pathway analysis
- Stable Isotope probing in Environmental microbiology
- Environmental monitoring applications
Features and Benefits
Features
Benefits
- 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.
General description
Acetanilide-(ring-13C6, carbonyl-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.
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.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
321.8 °F - closed cup
flash_point_c
161.00 °C - closed cup
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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