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I6035

Sigma-Aldrich

L-Iditol

≥98% (GC)

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About This Item

Empirische Formel (Hill-System):
C6H14O6
CAS-Nummer:
488-45-9
Molekulargewicht:
182.17
MDL-Nummer:
MFCD00064289
UNSPSC-Code:
12352201
PubChem Substanz-ID:
329815389
NACRES:
NA.25

Qualitätsniveau

100

Assay

≥98% (GC)

Form

solid

Farbe

white

mp (Schmelzpunkt)

78-80 °C (lit.)

Löslichkeit

water: 50 mg/mL, clear, colorless

Lagertemp.

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

InChIKey

FBPFZTCFMRRESA-UNTFVMJOSA-N

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Allgemeine Beschreibung

A rare sugar alcohol (polyol).

Sonstige Hinweise

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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D-Psicose ≥95% (HPLC)

Sigma-Aldrich

P8043

D-Psicose

D-Mannitol ≥98% (GC)

Sigma-Aldrich

M4125

D-Mannitol

Dextromethorphan HBr certified reference material, pharmaceutical secondary standard

Supelco

PHR1018

Dextromethorphan HBr

D-Sorbit ≥98% (GC)

Sigma-Aldrich

S1876

D-Sorbit

D-Sorbit 99% (GC)

Sigma-Aldrich

240850

D-Sorbit

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
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
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
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