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250287

Sigma-Aldrich

1,10-Diiododecane

95%

Synonym(s):

Decamethylene diiodide

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About This Item

Linear Formula:
I(CH2)10I
CAS Number:
Molecular Weight:
394.07
Beilstein/REAXYS Number:
1738614
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

95%

form

liquid

bp

197-200 °C/12 mmHg (lit.)

mp

33-35 °C (lit.)

functional group

iodo

SMILES string

ICCCCCCCCCCI

InChI

1S/C10H20I2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-10H2

InChI key

CKJCTZAIDVFHCX-UHFFFAOYSA-N

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General description

Electrochemical reduction of 1,10-diiododecane at Hg cathode in dimethylformamide containing tetramethylammonium perchlorate has been investigated.

Application

1,10-Diiododecane has been used as:
  • an alkylating agent in the synthesis of symmetrical and unsymmetrical bis-cryptophanes
  • crosslinking reagent for tetrabutylammonium polygalacturonic acid

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Gelation of chemically cross-linked polygalacturonic acid derivatives.
Matricardi P, et al.
Carbohydrate Polymers, 27(3), 215-220 (1995)
Electrochemical reduction of 1, 10-dihalodecanes at mercury cathodes in dimethylformamide.
Bart JC and Peters DG.
J. Electroanal. Chem. Interfac. Electrochem., 280(1), 129-144 (1990)
Magali Darzac et al.
Chemical communications (Cambridge, England), (1)(1), 48-49 (2002-07-18)
After deprotection with a palladium catalyst, mono-allylated cryptophane-A (1, 2) and cryptophane-E (3) gave the new cryptophanols 4, 5 and 6, respectively, which are important key compounds for the preparation of monofunctionalized cryptophanes as well as for the design of

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