L-IDITOL
- CAS NO.:488-45-9
- Empirical Formula: C6H14O6
- Molecular Weight: 182.17
- MDL number: MFCD00064289
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-05-04 17:34:39
What is L-IDITOL?
Chemical properties
Off-White Crystalline Solid
The Uses of L-IDITOL
Occurs naturally along with D-Glucitol in plants, including in the berry of mountain ash (Sorbus aucuparia). Allitol, D-talitol and L-iditol are sugar alcohols that are rare in nature.
What are the applications of Application
L-Iditol is a naturally occurring plant compound
Definition
ChEBI: L-iditol is the L-enantiomer of iditol. It has a role as a fungal metabolite and a human metabolite. It is an enantiomer of a D-iditol.
Properties of L-IDITOL
Melting point: | 77 °C |
Boiling point: | 235.55°C (rough estimate) |
Density | 1.2393 (rough estimate) |
refractive index | -3 ° (C=1, H2O) |
storage temp. | -20°C Freezer |
solubility | DMSO (Slightly, Sonicated), Methanol (Slightly), Water (Slightly, Sonicated) |
pka | 13.14±0.20(Predicted) |
form | Crystalline Powder |
color | White |
Safety information for L-IDITOL
Computed Descriptors for L-IDITOL
New Products
4-Aminotetrahydropyran-4-carbonitrile Hydrochloride (R)-3-Aminobutanenitrile Hydrochloride 4-AMINO-TETRAHYDRO-PYRAN-4-CARBOXYLIC ACID HCL 4-(Dimethylamino)tetrahydro-2H-pyran-4-carbonitrile 3-((Dimethylamino)methyl)-5-methylhexan-2-one oxalate 1,4-Dioxa-8-azaspiro[4.5]decane 5-Bromo-2-nitropyridine Nimesulide BP Aceclofenac IP/BP/EP Diclofenac Sodium IP/BP/EP/USP Mefenamic Acid IP/BP/EP/USP Ornidazole IP Diclofenac Potassium SODIUM AAS SOLUTION ZINC AAS SOLUTION BUFFER SOLUTION PH 10.0(BORATE) GOOCH CRUCIBLE SINTERED AQUANIL 5 BERYLLIUM AAS SOLUTION 2-Bromo-1-(bromomethyl)-3-chloro-5-nitrobenzene 2-Bromo-3-nitroaniline N-(3-Hydroxypropyl)-N-methylacetamide 3-Bromo-6-chloropyridazine 4-ethyl-3-nitrobenzoic acidRelated products of tetrahydrofuran
6-PHOSPHOGLUCONIC ACID BARIUM SALT
D-MYO-INOSITOL 2,4-BIS-PHOSPHATE AMMONIUM SALT
MYO-INOSITOL HEXASULFATE HEXAPOTASSIUM SALT
1,2-O-ISOPROPYLIDENE-BETA-L-IDOFURANOSE
L-IDITOL
L-(-)-IDOSE
INS(1,4)P2
D-INS(1,4,5)P3, 3LI
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