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251860

Sigma-Aldrich

1-Iodononane

95%

Synonym(s):

Nonyl iodide

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About This Item

Linear Formula:
CH3(CH2)8I
CAS Number:
4282-42-2
Molecular Weight:
254.15
EC Number:
224-286-3
MDL number:
MFCD00001107
UNSPSC Code:
12352100
PubChem Substance ID:
24855162
NACRES:
NA.22

Quality Level

200

Assay

95%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.487 (lit.)

bp

107-108 °C/8 mmHg (lit.)

density

1.288 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCI

InChI

1S/C9H19I/c1-2-3-4-5-6-7-8-9-10/h2-9H2,1H3

InChI key

OGSJMFCWOUHXHN-UHFFFAOYSA-N

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Application

1-Iodononane has been used in the synthesis of:
  • Sch II, a cerebroside that induces fruiting body formation in the basidiomycete Schizophyllum commune
  • 2,6-dimethyl-4-nonylpyridine
  • 2-tridecanone

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

185.0 °F - closed cup

Flash Point(C)

85 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF3635
BCCC4923
BCBZ3177
BCBT3824
BCBQ9913V

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Sulfone-mediated synthesis of polysubstituted pyridines.
Craig D and Henry GD.
Tetrahedron Letters, 46(15), 2559-2562 (2005)
Fiona J Black et al.
Organic & biomolecular chemistry, 8(5), 1188-1193 (2010-02-19)
(4E,8E,10E)-9-Methyl-4,8,10-sphingatrienine, a core component of marine sphingolipids, was synthesised for the first time using a copper(I)-mediated 1,2-metallate rearrangement of a lithiated glycal as a key step. It was converted to phalluside-1, a cerebroside isolated from the ascidian Phallusia fumigate. By
Ultrasound mediated synthesis of a few naturally occurring compounds.
Singh J, et al.
Indian J. Chem. B, 40(5), 386-390 (2005)

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