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277185

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

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Certificados de análisis (COA)

Lot/Batch Number
MBBD7197
MBBD3013
MBBD0276
MBBC8019
MBBC7075

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Si necesita una versión concreta, puede buscar un certificado específico por el número de lote.

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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
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
Sarah J Feakins et al.
Rapid communications in mass spectrometry : RCM, 27(3), 430-436 (2013-01-03)
A published method to determine the hydrogen isotope ((2)H/(1)H) ratios of methoxyl groups, cleaved from lignin by hydroiodic acid (HI), calls for the analysis of methyl iodide (CH(3)I). However, analysis of halogenated compounds by gas chromatography/pyrolysis/isotope ratio mass spectrometry (GC/P/IRMS)
R Otto et al.
Nature chemistry, 4(7), 534-538 (2012-06-22)
Solvents have a profound influence on chemical reactions in solution and have long been used to control their outcome. Such effects are generally considered to be governed by thermodynamics; however, little is known about the steric effects of solvent molecules.
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