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Key Documents

Otros documentos

I6035

Sigma-Aldrich

L-Iditol

≥98% (GC)

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About This Item

Fórmula empírica (notación de Hill):
C6H14O6
Número de CAS:
488-45-9
Peso molecular:
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

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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)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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D-Manitol ≥98% (GC)

Sigma-Aldrich

M4125

D-Manitol

Dextromethorphan HBr certified reference material, pharmaceutical secondary standard

Supelco

PHR1018

Dextromethorphan HBr

D-Sorbitol ≥98% (GC)

Sigma-Aldrich

S1876

D-Sorbitol

D-Sorbitol 99% (GC)

Sigma-Aldrich

240850

D-Sorbitol

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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