L-Mannitol - ≥97% , CAS No.643-01-6

CAS: 643-01-6 Cat. No.: L130871 Formula: C₆H₁₄O₆ Peso molecolare: 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

Sinonimi

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

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 528765190
• Sorrisi canonici: 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
• Isomeri SMILES: C([C@@H]([C@@H]([C@H]([C@H](CO)O)O)O)O)O
• Peso molecolare: 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
• Descrizione: 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

Proprietà chimiche e fisiche

• Sensibilità: Hygroscopic
• Rotazione specifica [α]: -30° (C=5,H2O)
• Punto di fusione (°C): 165 °C
• Peso molecolare: 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