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Sigma-Aldrich

Iodomethane-13C

99 atom % 13C, 99% (CP), contains copper as stabilizer

Sinónimos:

13C Labeled iodomethane, Methyl-13C iodide

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About This Item

Fórmula lineal:
13CH3I
Número de CAS:
4227-95-6
Peso molecular:
142.93
Beilstein/REAXYS Number:
1697017
MDL number:
MFCD00001075
UNSPSC Code:
12352101
PubChem Substance ID:
24856740
NACRES:
NA.13

vapor density

4.89 (vs air)

Quality Level

200

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

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Categorías relacionadas

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.

For use with

Referencia del producto
Descripción
Precios

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
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
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
Sébastien Allard et al.
Water research, 44(15), 4623-4629 (2010-06-29)
This paper demonstrates that manganese oxides can initiate the formation of methyl iodide, a volatile compound that participates to the input of iodine into the atmosphere. The formation of methyl iodide was investigated using a natural manganese oxide in batch
Warayuth Sajomsang et al.
International journal of biological macromolecules, 50(1), 263-269 (2011-11-22)
Five water-soluble chitosan derivatives were carried out by quaternizing either iodomethane or N-(3-chloro-2-hydroxypropyl) trimethylammonium chloride (Quat188) as a quaternizing agent under basic condition. The degree of quaternization (DQ) ranged between 28±2% and 90±2%. The antifungal activity was evaluated by using
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