Skip to Content
MilliporeSigma
All Photos(2)

Key Documents

View All Documentation

I6035

Sigma-Aldrich

L-Iditol

≥98% (GC)

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C6H14O6
CAS Number:
488-45-9
Molecular Weight:
182.17
MDL number:
MFCD00064289
UNSPSC Code:
12352201
PubChem Substance ID:
329815389
NACRES:
NA.25

Quality Level

100

assay

≥98% (GC)

form

solid

color

white

mp

78-80 °C (lit.)

solubility

water: 50 mg/mL, clear, colorless

storage temp.

2-8°C

SMILES string

OC[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)CO

InChI

1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4-,5+,6+/m0/s1

InChI key

FBPFZTCFMRRESA-UNTFVMJOSA-N

Looking for similar products? Visit Product Comparison Guide

General description

A rare sugar alcohol (polyol).

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Wojciech Schönemann et al.
Bioorganic & medicinal chemistry, 18(7), 2645-2650 (2010-03-17)
A short synthesis of new beta-1-C-alkyl-1,5-dideoxy-1,5-imino-l-iditols by means of the diastereoselective addition of Grignard reagents onto a glucopyranosylamine is described. These compounds were evaluated as beta-glucocerebrosidase inhibitors and their activity was compared with that of related iminosugar derivatives in the
Hexitol anhydrides; 1,4,3,6-dianhydro-L-iditol and the structures of isomannide and isosorbide.
H G FLETCHER et al.
Journal of the American Chemical Society, 68, 939-941 (1946-06-01)
David M Hodgson et al.
Organic letters, 7(12), 2305-2308 (2005-06-04)
[reaction: see text] Reaction of hindered lithium amides with readily available (enantiopure) terminal epoxides gives 2-ene-1,4-diols via carbenoid dimerization of the corresponding alpha-lithiated epoxides. D-Mannitol and D-iditol were synthesized using this method in three steps from (S)-tritylglycidyl ether.
Constitution of the dianhydrides of sorbitol and iditol.
R MONTGOMERY et al.
Nature, 157, 372-372 (1946-03-23)
N A Williams et al.
Journal of parenteral science and technology : a publication of the Parenteral Drug Association, 47(3), 119-123 (1993-05-01)
The mechanical properties of frozen mannitol, L-iditol, dulcitol, and sorbitol solutions were measured as a function of temperature during warming (after freezing) using a thermal mechanical analyzer (TMA). The mannitol sample first underwent a contractive phase starting at 30 degrees
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service