ChemicalBook--->CAS DataBase List--->75-11-6

75-11-6

75-11-6 Structure

75-11-6 Structure
IdentificationMore
[Name]

Diiodomethane
[CAS]

75-11-6
[Synonyms]

DIIODOMETHANE
METHYLENE DIIODIDE
METHYLENE IODIDE
CH2I2
Diiodmethan
diiodo-methan
Diiodomethane,methyleneiodide
Dijodmethan
ioduredemethylene
Methane,diiodo-
Methyl diiodide
Methylenjodid
Mi-gee
Mi-gee brand
Diodomethane
DIIODOMETHANE REAGENTPLUS(TM) 99%
DIIODOMETHANE, REAGENTPLUS, 99%
METHYLENE IODIDE STAB.
Diiodomethane(ForSeparationOfMinerals)
Diiodomethane,99%
[EINECS(EC#)]

200-841-5
[Molecular Formula]

CH2I2
[MDL Number]

MFCD00001079
[Molecular Weight]

267.84
[MOL File]

75-11-6.mol
Chemical PropertiesBack Directory
[Appearance]

light yellow or gold liquid with chloroform-like odour
[Melting point ]

6 °C
[Boiling point ]

67-69 °C11 mm Hg(lit.)
[density ]

3.325 g/mL at 25 °C(lit.)
[vapor density ]

9.25 (vs air)
[refractive index ]

1.737
[Fp ]

181°C
[storage temp. ]

Store below +30°C.
[solubility ]

0.8g/l
[form ]

Liquid
[color ]

deep yellow
[Specific Gravity]

3.325
[Stability:]

Stable. Incompatible with strong oxidizing agents, strong bases. Reacts violently with alkali metal salts. May discolour on exposure to light.
[Water Solubility ]

14 g/L (20 ºC)
[Specific Heat Capacity]

Cp(liquid):134J/(g·K);Cp(gas):0.215427J/(g·K),at 25℃
[Thermal Conductivity]

0.098 W/(m·K) at 25 ℃
[Sensitive ]

Light Sensitive
[Merck ]

14,6066
[BRN ]

1696892
[Henry's Law Constant]

2.3×10-2 mol/(m3Pa) at 25℃, Burkholder et al. (2019)
[Dielectric constant]

5.3(-4℃)
[InChI]

1S/CH2I2/c2-1-3/h1H2
[InChIKey]

NZZFYRREKKOMAT-UHFFFAOYSA-N
[SMILES]

ICI
[Surface tension]

50.8mN/m at 20°C
[CAS DataBase Reference]

75-11-6(CAS DataBase Reference)
[NIST Chemistry Reference]

Methane, diiodo-(75-11-6)
[EPA Substance Registry System]

75-11-6(EPA Substance)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H301+H311-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P301+P310-P302+P352+P312-P304+P340+P312-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[RIDADR ]

2810
[WGK Germany ]

3
[RTECS ]

PA8575000
[F ]

8
[TSCA ]

Yes
[REACH Registrations]

Active
[HazardClass ]

6.1
[PackingGroup ]

III
[HS Code ]

29033080
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Chronic 3
[Toxicity]

LD50 orally in Rabbit: 76 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Benzyltriethylammonium chloride-->Iodoform
[Preparation Products]

N,N-DiMethylMethyleneaMMoniuM Iodide-->3,4-(Methylenedioxy)phenyl isocyanate-->3,4-(Methylenedioxy)phenylacetic acid-->Piperonyloyl chloride-->Cyclopropyl carbinol-->4-Bromo-7-methoxy-benzo[1,3]dioxole-5-carboxylic acid methyl ester-->Bis(phenylthio)methane-->Cyclopropane-->Methyl 3-methoxy-4,5-methylenedioxybenzoate-->Diethyl (hydroxymethyl)phosphonate-->Diethyl iodomethylphosphonate-->Bis(2-methoxyethoxy)methane-->1-methyl-4-[(4-methylphenyl)sulfonyloxymethoxysulfonyl]benzene-->Fluoroiodomethane-->1-Phenyl-1-cyclopropanol
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Diiodomethane(75-11-6).msds
Hazard InformationBack Directory
[Hazard]

May be irritating and narcotic.
[Description]

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
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.
https://www.sigmaaldrich.com/catalog/product/sial/158429
[Chemical Properties]

light yellow or gold liquid with chloroform-like odour
[Uses]

Diiodomethane is used to determine the density of minerals and other solid samples due to its high density. It is used as an optical contact liquid to determine the refractive index of certain gemstones. In simmons-smith reaction, it acts as a reagent to generate methylene (carbine) free radical. It reacts with olefins to prepare cyclopropanes with high stereo specificity.
[Uses]

In separating mixtures of minerals. In determining the specific gravity of minerals and other substances. In the manufacture of x-ray contrast media.
[Application]

Diiodomethane is used as the dispersive (non-polar) liquid while de-ionized water and glycerol as polar liquids. It is also used in separating mixtures of minerals. In determining the specific gravity of minerals and other substances. In the manufacture of x-ray contrast media.
[General Description]

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.
[Synthesis]

Diiodomethane can be prepared from the widely available solvent dichloromethane by the action of sodium iodide in acetone in the Finkelstein reaction:
CH2Cl2 + 2 NaI → CH2I2 + 2 NaCl.
It can also be prepared by reducing iodoform with elemental phosphorus or sodium arsenite:
CHI3 + Na3AsO3 + NaOH → CH2I2 + NaI + Na3AsO.
Diiodomethane is prepared by reacting iodoform with sodium acetate in ethanol.
[Purification Methods]

Fractionally distil it under reduced pressure, then fractionally crystallise it by partial freezing, and stabilize it with silver wool if necessary. It has also been purified by drying over CaCl2 and fractionally distilling from Cu powder. Store it in the dark. [Beilstein 1 IV 97.]
Spectrum DetailBack Directory
[Spectrum Detail]

Diiodomethane(75-11-6)MS
Diiodomethane(75-11-6)1HNMR
Diiodomethane(75-11-6)13CNMR
Diiodomethane(75-11-6)IR1
Diiodomethane(75-11-6)IR2
Diiodomethane(75-11-6)ESR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Diiodomethane, stabilized, 99+%(75-11-6)
[Alfa Aesar]

Diiodomethane, 99%, stab. with copper wire(75-11-6)
[Sigma Aldrich]

75-11-6(sigmaaldrich)
[TCI AMERICA]

Diiodomethane  (stabilized with Copper chip),>98.0%(GC)(75-11-6)
75-11-6 suppliers list
Company Name: Shanghai YouPeng Chemical Co. Ltd.  Gold
Telephone: 021-69005955 13701776567;
Website: http://www.youpengchem.com
Company Name: Shanghai Witofly Chemical Co. ,Ltd.  Gold
Telephone: 02150630626 17717886015
Website: www.witofly.com
Company Name: Yangzhou Prince Chemical Co., Ltd  Gold
Telephone: 0514-84248359 13328140016;15052570758;15949050037
Website: www.princechem.com
Company Name: Manac (SHANGHAI) TRADING CO., LTD  Gold
Telephone: 021-32503616
Website: http://manac-inc.com.cn
Company Name: Hubeicowardchemical  Gold
Telephone: 027-83295551 13317178958
Website: www.cowardchemical.com/
Company Name: Shanghai Qiji Yongying Biotechnology Co., Ltd.  Gold
Telephone: 13069481218
Website:
Company Name: Wuhan xinyangruihe Chemical Technology Co., Ltd.  Gold
Telephone: 153-07155313 15307155313
Website: http://www.ruihechem.com/
Company Name: Shandong Xiya Chemical Co., Ltd.  Gold
Telephone: 4009903999 13395398332
Website: http://www.xiyashiji.com
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Telephone: 021-50182298 021-50180596
Website: www.boylechem.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Telephone: 4006356688 18621169109
Website: www.x-labseek.com/
Company Name: Beijing Donghualituo Techonlogy Development Co.,Ltd.  
Telephone: 010-88425576
Website: www.dhltchem.com
Company Name: Anqing PhiChem Corporation  
Telephone: 0556-5209970
Website: http://www.phichem.com.cn
Company Name: Shanghai Gonghe Chemical Co., Ltd  
Telephone: +86-21-56733000
Website: www.gonghechem.com
Company Name: Alfa Aesar  
Telephone: 400-6106006
Website: http://chemicals.thermofisher.cn
Company Name: TCI (Shanghai) Development Co., Ltd.  
Telephone: 021-67121386
Website: https://www.tcichemicals.com/CN/zh/
Company Name: Energy Chemical  
Telephone: 400-0056266
Website: www.energy-chemical.com
Company Name: JinYan Chemicals(ShangHai) Co.,Ltd.  
Telephone: 13817811078
Website: www.jingyan-chemical.com
Company Name: Jia Xing Isenchem Co.,Ltd  
Telephone: 0573-85285100 18627885956
Website: https://www.chemicalbook.com/ShowSupplierProductsList14265/0_EN.htm
Tags:75-11-6 Related Product Information
75-47-8 2314-97-8 74-88-4 7553-56-2 101-68-8 25535-16-4 507-25-5 513-92-8 20018-09-1 75-11-6