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α-L-Rhamnose monohydrate - 10mM in DMSO, high purity , CAS No.6155-35-7

    Grade & Purity:
  • 10mM in DMSO
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Item Number
L425101
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L425101-1ml
1ml
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$42.90
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Compound libraries (12325)

Basic Description

Synonyms 6155-35-7 | L-Rhamnose monohydrate | alpha-L-Rhamnose monohydrate | (2R,3R,4R,5R,6S)-6-methyloxane-2,3,4,5-tetrol;hydrate | (2R,3R,4R,5R,6S)-6-methyltetrahydro-2H-pyran-2,3,4,5-tetraol hydrate | MFCD00071591 | alpha-L-Mannopyranose, 6-deoxy-, hydrate (1:1); Rhamnopyr
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms α-L-Rhamnose monohydrate (6-deoxy-L-mannose monohydrate, α-L-Rhamnopyranose monohydrate) is used as a starting material for the production of furanones. It is an important material involved in the reaction of flavors developed during the preparation of va
Storage Temp Store at -80°C
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Product Description

Information

α-L-Rhamnose monohydrate (6-deoxy-L-mannose monohydrate, α-L-Rhamnopyranose monohydrate) is used as a starting material for the production of furanones. It is an important material involved in the reaction of flavors developed during the preparation of various foods like bread, grilled meats, etc.

In vitro

L-rhamnose in concentration up to 20 (32 resp.) mmol/l can not be considered as cytotoxic or cytostatic for the used in vitro tumor models.

In vivo

L-rhamnose exerts a significant suppressive effect on tumour growth. Its optimal dose is estimated to be 3.64 g/kg/day.

Cell Research(from reference)

Concentrations:0.125 mmol/l to 32 mmol/l 

Incubation Time:48 h 

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct Parent Hexoses
Alternative Parents Oxanes  Secondary alcohols  Hemiacetals  1,2-diols  Oxacyclic compounds  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteromonocyclic compounds
Substituents Hexose monosaccharide - Oxane - Secondary alcohol - Hemiacetal - 1,2-diol - Oxacycle - Organoheterocyclic compound - Polyol - Organic oxide - Hydrocarbon derivative - Alcohol - Aliphatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
External Descriptors Not available

Product Properties

ALogP -1.833
hba_count 1
HBD Count 3

Names and Identifiers

IUPAC Name (2R,3R,4R,5R,6S)-6-methyloxane-2,3,4,5-tetrol;hydrate
INCHI InChI=1S/C6H12O5.H2O/c1-2-3(7)4(8)5(9)6(10)11-2;/h2-10H,1H3;1H2/t2-,3-,4+,5+,6+;/m0./s1
InChIKey BNRKZHXOBMEUGK-NRBMBCGPSA-N
Smiles CC1C(C(C(C(O1)O)O)O)O.O
Isomeric SMILES C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O)O)O)O.O
Molecular Weight 182.17
Reaxy-Rn 36982352
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=36982352&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

DMSO(mg / mL) Max Solubility 36
DMSO(mM) Max Solubility 197.6176099
Molecular Weight 182.170 g/mol
XLogP3
Hydrogen Bond Donor Count 5
Hydrogen Bond Acceptor Count 6
Rotatable Bond Count 0
Exact Mass 182.079 Da
Monoisotopic Mass 182.079 Da
Topological Polar Surface Area 91.200 Ų
Heavy Atom Count 12
Formal Charge 0
Complexity 139.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 5
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 2

Citations of This Product

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