lactitol
chemical compound
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lactitol
Summary
lactitol is a type of chemical entity[1]. lactitol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (102 views/month).[2]
Key Facts
- lactitol's instance of is recorded as type of chemical entity[3].
- lactitol's canonical SMILES is recorded as C(C1C(C(C(C(O1)OC(C(CO)O)C(C(CO)O)O)O)O)O)O[4].
- lactitol's chemical formula is recorded as C₁₂H₂₄O₁₁[5].
- lactitol is a type of disaccharide[6].
- lactitol is used for sweetener[7].
- lactitol's Commons category is recorded as Lactitol[8].
- lactitol comprises oxygen[9].
- lactitol comprises carbon[10].
- lactitol comprises hydrogen[11].
- lactitol's isomeric SMILES is recorded as C([C@@H]1C@@HO)OC@@HO)O">[12].
- lactitol's mass is recorded as {'unit': 'Q483261', 'amount': '+344.131862'}[13].
- lactitol's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'lactitol'}[14].
- lactitol's subject has role is recorded as cathartic[15].
- lactitol's stereoisomer of is recorded as α-D-Glcp-(1→3)-D-Glc-OH[16].
- lactitol's stereoisomer of is recorded as β-D-Galp-(1→3)-D-Gal-OH[17].
- lactitol's stereoisomer of is recorded as cellobiotol[18].
- lactitol's stereoisomer of is recorded as maltitol[19].
- lactitol's stereoisomer of is recorded as β-D-Galp-(1→3)-Man-OH[20].
- lactitol's stereoisomer of is recorded as α-D-Manp-(1→3)-Man-OH[21].
- lactitol's stereoisomer of is recorded as β-D-Glcp-(1→3)-D-Glc-OH[22].
- lactitol's stereoisomer of is recorded as β-D-Galp-(1→4)-D-Gal-OH[23].
- lactitol's stereoisomer of is recorded as α-D-Galp-(1→4)-D-Gal-OH[24].
Why It Matters
lactitol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (102 views/month).[2] lactitol has Wikipedia articles in 21 language editions, a strong signal of global cultural recognition.[25] lactitol is known by 14 alternative names across languages and contexts.[26]