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About This Item
Empirical Formula (Hill Notation):
CH2I2
CAS Number:
Molecular Weight:
267.84
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
200-841-5
MDL number:
Beilstein/REAXYS Number:
1696892
Assay:
99%
Form:
liquid
Product Name
Diiodomethane, ReagentPlus®, 99%, contains copper as stabilizer
vapor density
9.25 (vs air)
product line
ReagentPlus®
assay
99%
form
liquid
contains
copper as stabilizer
bp
67-69 °C/11 mmHg (lit.)
mp
5-8 °C (lit.)
density
3.325 g/mL at 25 °C (lit.)
functional group
iodo
SMILES string
ICI
InChI
1S/CH2I2/c2-1-3/h1H2
InChI key
NZZFYRREKKOMAT-UHFFFAOYSA-N
General description
Diiodomethane is a solvent used as a halogen bond donor toward metal-bound halides.
Diiodomethane (CH2I2) is an iodine containing organic compound. Its decomposition in acetonitrile initiated by 310nm light has been investigated. Femtosecond pump-probe spectroscopic and ab initio molecular dynamics simulations studies of the photodecomposition of CH2I2 suggest the formation of the isomer of diiodomethane (CH2I-I) as hot photoproduct. In the atmosphere, it undergoes photolysis in the presence of ozone to afford iodine oxide (IO) which results in the formation of aerosols. Its vacuum ultraviolet (VUV) photoabsorption spectrum has been reported.
Diiodomethane (CH2I2) is an iodine containing organic compound. Its decomposition in acetonitrile initiated by 310nm light has been investigated. Femtosecond pump-probe spectroscopic and ab initio molecular dynamics simulations studies of the photodecomposition of CH2I2 suggest the formation of the isomer of diiodomethane (CH2I-I) as hot photoproduct. In the atmosphere, it undergoes photolysis in the presence of ozone to afford iodine oxide (IO) which results in the formation of aerosols. Its vacuum ultraviolet (VUV) photoabsorption spectrum has been reported.
Application
Diiodomethane has been used as a probe liquid for evaluation of the polar and dispersive components of the surface energy of the catecholamine coated fiber surfaces. It may be used for the preparation of cyclopropyl ketones, esters and amides.
Diiodomethane may be used as a probe solvent in contact angle measurement to analyze the hydrophilicity of polymer surfaces.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Anuvab Mandal et al.
The Journal of chemical physics, 140(19), 194312-194312 (2014-05-24)
The electronic absorption spectrum of diiodomethane in the 30,000-95,000 cm(-1) region is investigated using synchrotron radiation; the spectrum in the 50,000-66,500 cm(-1) region is reported for the first time. The absorption bands in the 30,000-50,000 cm(-1) region are attributed to
Nowsheen Goonoo et al.
Materials science & engineering. C, Materials for biological applications, 76, 13-24 (2017-05-10)
In this paper, the biomineralization potential and cellular response of novel blend films of the anionic sulfated polysaccharides kappa-carrageenan (KCG) and fucoidan (FUC) derived from seaweeds with semi-crystalline polyhydroxybutyrate (PHB) and polyhydroxybutyrate-co-valerate (PHBV), respectively, were analyzed. The incorporation of KCG
Catecholamine polymers as surface modifiers for enhancing interfacial strength of fiber-reinforced composites.
Lee W, et al.
Composites Science and Technology, 110, 53-61 (2015)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 158429-25G | 04061838743930 |
| 158429-100G | 04061838743923 |
| 158429-500G | 04061838743947 |