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The synthesis process is considered proprietary.
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316555
1,6-Anhydro-β-D-glucose
99%
Synonym(e):
Laevoglucosan
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1 G
€ 82,80
About This Item
Empirische Formel (Hill-System):
C6H10O5
CAS-Nummer:
Molekulargewicht:
162.14
Beilstein:
80998
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352201
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
99%
Form
powder or crystals
Optische Aktivität
[α]18/D −66°, c = 1 in H2O
Farbe
beige
mp (Schmelzpunkt)
182-184 °C (lit.)
Löslichkeit
water: 50 mg/mL, clear, colorless
SMILES String
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
InChIKey
TWNIBLMWSKIRAT-VFUOTHLCSA-N
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Anwendung
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]
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
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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Bailliez V, et al.
Tetrahedron, 60(5), 1079-1085 (2004)
The controlled synthesis of polyglucose in one-dimensional coordination nanochannels
Kobayashi Y, et al.
Chemical Communications (Cambridge, England), 52(29), 5156-5159 (2016)
Synthesis of Protected 3-Deoxy-3-fluoro-and 4-Deoxy-4-fluoro-d-galactopyranosides from Levoglucosan
Laine D, et al.
The Journal of Organic Chemistry, 82(9), 4986-4992 (2017)
Dimitra Balla et al.
Environmental science and pollution research international, 25(13), 12191-12205 (2017-09-10)
Two classes of polar organic compounds, dicarboxylic acids (DCAs) and sugars/sugar anhydrides (S/SAs), were measured in airborne particulate matter in the area of Thessaloniki, northern Greece. The target compounds were measured simultaneously in two particle fractions PM10 and PM2.5 during
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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 answer-
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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