277185
Iodomethane-13C
99 atom % 13C, 99% (CP), contains copper as stabilizer
Synonym(s):
13C Labeled iodomethane, Methyl-13C iodide
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
13CH3I
CAS Number:
Molecular Weight:
142.93
UNSPSC Code:
12352101
NACRES:
NA.13
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1697017
Isotopic purity:
99 atom % 13C
Assay:
99% (CP)
Mass shift:
M+1
Form:
liquid
vapor density
4.89 (vs air)
Quality Level
vapor pressure
6.35 psi ( 20 °C)
isotopic purity
99 atom % 13C
assay
99% (CP)
form
liquid
contains
copper as stabilizer
technique(s)
protein expression: suitable
refractive index
n20/D 1.5293 (lit.)
bp
42 °C (lit.)
mp
−66.5 °C (lit.)
density
2.290 g/mL at 25 °C
application(s)
environmental
mass shift
M+1
storage temp.
2-8°C
SMILES string
[13CH3]I
InChI
1S/CH3I/c1-2/h1H3/i1+1
InChI key
INQOMBQAUSQDDS-OUBTZVSYSA-N
General description
13CH3I, isotopically labeled methyl iodide.
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
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Carc. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Shu-Yu Zhang et al.
Journal of the American Chemical Society, 135(32), 12135-12141 (2013-08-08)
We report a new set of reactions based on the Pd-catalyzed alkylation of methylene C(sp(3))-H bonds of aliphatic quinolyl carboxamides with α-haloacetate and methyl iodide and applications in the stereoselective synthesis of various β-alkylated α-amino acids. These reactions represent the
Susan E Cellitti et al.
Journal of the American Chemical Society, 130(29), 9268-9281 (2008-06-26)
In vivo incorporation of isotopically labeled unnatural amino acids into large proteins drastically reduces the complexity of nuclear magnetic resonance (NMR) spectra. Incorporation is accomplished by coexpressing an orthogonal tRNA/aminoacyl-tRNA synthetase pair specific for the unnatural amino acid added to
Gerardo Alvarez-Manilla et al.
Glycobiology, 17(7), 677-687 (2007-03-27)
Analysis of oligosaccharides by mass spectrometry (MS) has enabled the investigation of the glycan repertoire of organisms with high resolution and sensitivity. It is difficult, however, to correlate the expression of glycosyltransferases with the glycan structures present in a particular