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The synthesis process is considered proprietary.
316555
1,6-Anhydro-β-D-glucose
99%
Synonyme(s) :
Levoglucosan
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82,80 €
About This Item
Formule empirique (notation de Hill):
C6H10O5
Numéro CAS:
Poids moléculaire :
162.14
Beilstein:
80998
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352201
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Essai
99%
Forme
powder or crystals
Activité optique
[α]18/D −66°, c = 1 in H2O
Couleur
beige
Pf
182-184 °C (lit.)
Solubilité
water: 50 mg/mL, clear, colorless
Chaîne SMILES
O[C@H]1[C@H](O)[C@H]2CO[C@H](O2)[C@@H]1O
InChI
1S/C6H10O5/c7-3-2-1-10-6(11-2)5(9)4(3)8/h2-9H,1H2/t2-,3-,4+,5-,6-/m1/s1
Clé InChI
TWNIBLMWSKIRAT-VFUOTHLCSA-N
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Application
1,6-Anhydro-β-D-glucose (Levoglucosan) can be used as a precursor for the synthesis of:
- 1,6-anhydro-2,4-dideoxy-β-D-glycerohexopyranos-3-ulose.[1]
- Quasi-linear polyglucose (PGlc) via cationic ring-opening polymerization.[2]
- Polynitrogenated analogs of glucopyranoses.[3]
- 3-deoxy-3-fluorogalactopyranose and acetylated 4-deoxy-4-fluorogalactopyranose.[4]
Autres remarques
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Can you please elucidate in detail the synthesis process? What exactly is the process flow?
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What is the method of manufacture for product 316555, 1,6-Anhydro-β-D-glucose?
1 réponse-
Product 316555, 1,6-Anhydro-β-D-glucose, is manufactured by the pyrolysis of starch. The solvents used in the process are water, ethanol, and methanol.
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What is the Department of Transportation shipping information for this product?
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Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
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