456756
Iodomethane solution
2.0 M in tert-butyl methyl ether, contains copper as stabilizer
Sinonimo/i:
Methyl iodide
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About This Item
Formula empirica (notazione di Hill):
CH3I
Numero CAS:
Peso molecolare:
141.94
Beilstein:
969135
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.21
Prodotti consigliati
Tensione di vapore
16.85 psi ( 55 °C)
4.86 psi ( 20 °C)
Livello qualitativo
contiene
copper as stabilizer
Concentrazione
2.0 M in tert-butyl methyl ether
P. ebollizione
41-43 °C
Densità
0.933 g/mL at 25 °C
Gruppo funzionale
alkyl halide
iodo
Temperatura di conservazione
2-8°C
Stringa SMILE
CI
InChI
1S/CH3I/c1-2/h1H3
INQOMBQAUSQDDS-UHFFFAOYSA-N
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Descrizione generale
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.
Applicazioni
- 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).
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Irrit. 2
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
-0.4 °F
Punto d’infiammabilità (°C)
-18 °C
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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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