L-Mannitol - ≥97% , CAS No.643-01-6

CAS: 643-01-6 Cat. No.: L130871 Formule: C₆H₁₄O₆ Poids moléculaire: 182.17

GRADE & PURITY ≥97%

Synonyms

MFCD00154039 | SCHEMBL25330 | GEO-04675 | J-200008 | F0430C81-EA3D-4324-863D-08AB2852F39D | M1084 | Q27117350 | D-Mannitol, EP, USP grade | FBPFZTCFMRRESA-BXKVDMCESA-N | W-203389 | L-Mannitol | AC-13700 | CHEBI:38030 | (2S,3S,4S,5S)-hexane-1,2,3,4,5,6-hex

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonymes

MFCD00154039 | SCHEMBL25330 | GEO-04675 | J-200008 | F0430C81-EA3D-4324-863D-08AB2852F39D | M1084 | Q27117350 | D-Mannitol, EP, USP grade | FBPFZTCFMRRESA-BXKVDMCESA-N | W-203389 | L-Mannitol | AC-13700 | CHEBI:38030 | (2S,3S,4S,5S)-hexane-1,2,3,4,5,6-hex

Spécifications et pureté

≥97%

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥97%

Noms et identifiants

• Pubchem Sid: 528765190
• Sourires canoniques: C(C(C(C(C(CO)O)O)O)O)O
• IUPAC Name: (2S,3S,4S,5S)-hexane-1,2,3,4,5,6-hexol
• InChIKey: FBPFZTCFMRRESA-BXKVDMCESA-N
• 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
• Isomères SMILES: C([C@@H]([C@@H]([C@H]([C@H](CO)O)O)O)O)O
• Poids moléculaire: 182.17
• Reaxy-Rn: 8496933
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8496933&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar alcohols
• Alternative Parents: Monosaccharides Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
• External Descriptors: mannitol

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Sensibilité: Hygroscopic
• Rotation spécifique [α]: -30° (C=5,H2O)
• Point de fusion (°C): 165 °C
• Poids moléculaire: 182.170 g/mol
• XLogP3: -3.100
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 182.079 Da
• Monoisotopic Mass: 182.079 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 105.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1