Saltar al contenido
Merck

456756

Iodomethane solution

2.0 M in tert-butyl methyl ether, solution, contains copper as stabilizer

Sinónimos:

Methyl iodide

para ver los precios por organización y contrato.

Seleccione un Tamaño

Cambiar Vistas

Acerca de este artículo

Fórmula empírica (notación de Hill):
CH3I
Número CAS:
Peso molecular:
141.94
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
969135
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarle


Nombre del producto

Iodomethane solution, 2.0 M in tert-butyl methyl ether, contains copper as stabilizer

Quality Segment

vapor pressure

16.85 psi ( 55 °C), 4.86 psi ( 20 °C)

contains

copper as stabilizer

concentration

2.0 M in tert-butyl methyl ether

bp

41-43 °C

density

0.933 g/mL at 25 °C

functional group

alkyl halide, iodo

storage temp.

2-8°C

SMILES string

CI

InChI

1S/CH3I/c1-2/h1H3

InChI key

INQOMBQAUSQDDS-UHFFFAOYSA-N

General description

The product is 2M solution of iodomethane in tert-butyl methyl ether. Iodomethane also known as methyl iodide is an alkyl halide commonly employed as methylating agent.

Application

  • 8-plex LC-MS/MS Analysis of Permethylated N-Glycans Achieved by Using Stable Isotopic Iodomethane.: This research demonstrates the use of iodomethane in stable isotope labeling for the mass spectrometric analysis of permethylated N-glycans. The method enhances the accuracy and sensitivity of glycomic studies (Dong et al., 2019).
  • Comparative glycomic profiling of isotopically permethylated N-glycans by liquid chromatography/electrospray ionization mass spectrometry.: The study presents a comparative analysis of N-glycan profiles using isotopically labeled iodomethane, improving the resolution and identification of glycan structures in complex biological samples (Hu et al., 2013).
  • Antifungal property of quaternized chitosan and its derivatives.: This paper explores the synthesis of quaternized chitosan derivatives using iodomethane and their subsequent antifungal activities. The results suggest potential applications in biomedical and agricultural fields (Sajomsang et al., 2012).
  • Validation of two fluoro-analogues of N,N-dimethyl-2-(2′-amino-4′-hydroxymethyl-phenylthio)benzylamine as serotonin transporter imaging agents using microPET.: This research validates fluoro-analogues of a serotonin transporter imaging agent, synthesized using iodomethane, highlighting its potential in neuroimaging applications (Jarkas et al., 2010).


signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-0.4 °F

flash_point_c

-18 °C



Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documentos section.

Si necesita más asistencia, póngase en contacto con Atención al cliente

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos