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Merck
CN

250287

1,10-Diiododecane

95%

Synonym(s):

Decamethylene diiodide

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About This Item

Linear Formula:
I(CH2)10I
CAS Number:
16355-92-3
Molecular Weight:
394.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24855048
EC Number:
240-415-6
Beilstein/REAXYS Number:
1738614
MDL number:
MFCD00001086
Assay:
95%
Form:
liquid

Key Documents

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Product Name

1,10-Diiododecane, 95%

assay

95%

form

liquid

bp

197-200 °C/12 mmHg (lit.)

InChI key

CKJCTZAIDVFHCX-UHFFFAOYSA-N

InChI

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

SMILES string

ICCCCCCCCCCI

mp

33-35 °C (lit.)

functional group

iodo

Quality Level

100

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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

General description

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCD0400
BCCC0375
BCBV3012
BCBS2423V
BCBQ3833V

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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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