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I6035

Sigma-Aldrich

L-Iditol

≥98% (GC)

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Empirical Formula (Hill Notation):
C6H14O6
CAS Number:
Molecular Weight:
182.17
MDL number:
PubChem Substance ID:
NACRES:
NA.25

Quality Level

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

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1 of 4

This Item
M8892836504160
L-Iditol ≥98% (GC)

I6035

L-Iditol

Maltitol ≥98% (HPLC)

M8892

Maltitol

L-Rhamnose monohydrate suitable for microbiology, ≥99.0%, Naturally occurring deoxy sugar that is found primarily in plants and some bacteria

83650

L-Rhamnose monohydrate

Millipore

4160

L-Isoleucine

solubility

water: 50 mg/mL, clear, colorless

solubility

water: 50 mg/mL, clear, colorless

solubility

H2O: 0.1 g/mL, clear, colorless

solubility

water: ~4% (at RT)

form

solid

form

powder

form

powder

form

crystalline solid, crystals

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

10-30°C

storage temp.

15-25°C

color

white

color

white

color

-

color

white

mp

78-80 °C (lit.)

mp

149-152 °C (lit.)

mp

90-95 °C

mp

-

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)


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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.
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
C A Brearley et al.
The Biochemical journal, 314 ( Pt 1), 215-225 (1996-02-15)
We have undertaken an analysis of the inositol phosphates of Spirodela polyrhiza at a developmental stage when massive accumulation of InsP6 indicates that a large net synthesis is occurring. We have identified Ins3P, Ins(1,4)P2, Ins(3,4)P2 and possibly Ins(4,6)P2, Ins(3,4,6)P3, Ins(3,4,5,6)P4
Constitution of the dianhydrides of sorbitol and iditol.
R MONTGOMERY et al.
Nature, 157, 372-372 (1946-03-23)

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