The store will not work correctly when cookies are disabled.
JavaScript seems to be disabled in your browser.
For the best experience on our site, be sure to turn on Javascript in your browser.
This is a demo store. No orders will be fulfilled.
We use cookies to keep things working smoothly and to improve your experience.
Choose what’s okay for you below. See our Cookie Policy .
Accept Cookies
L(-)-Allose - 98%, high purity , CAS No.7635-11-2
Basic Description
Synonyms
AKOS015904448 | 3BU | L-Allose | SCHEMBL8625651 | EINECS 231-565-3 | aldehydo-L-allose | GZCGUPFRVQAUEE-MOJAZDJTSA-N | Q27117249 | (2S,3S,4S,5S)-2,3,4,5,6-pentahydroxyhexanal | CS-0031625 | CHEBI:37746 | aldehydo-L-allo-hexose | GEO-04661 | W-200611 | HY-
Specifications & Purity
≥98%
Storage Temp
Store at -20°C,Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic oxygen compounds
Class
Organooxygen compounds
Subclass
Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes
Monosaccharides
Direct Parent
Hexoses
Alternative Parents
Medium-chain aldehydes Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic acyclic compounds
Substituents
Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic 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
aldehydo-allose - L-allose
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.
Names and Identifiers
Pubchem Sid
488187469
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488187469
IUPAC Name
(2S,3S,4S,5S)-2,3,4,5,6-pentahydroxyhexanal
INCHI
InChI=1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5-,6+/m1/s1
InChIKey
GZCGUPFRVQAUEE-MOJAZDJTSA-N
Smiles
C(C(C(C(C(C=O)O)O)O)O)O
Isomeric SMILES
C([C@@H]([C@@H]([C@@H]([C@@H](C=O)O)O)O)O)O
Molecular Weight
180.16
Reaxy-Rn
1908976
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908976&ln=
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Sensitivity
Moisture sensitive
Melt Point(°C)
127-129°C
Molecular Weight
180.160 g/mol
XLogP3
-2.900
Hydrogen Bond Donor Count
5
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
5
Exact Mass
180.063 Da
Monoisotopic Mass
180.063 Da
Topological Polar Surface Area
118.000 Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
138.000
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
Solution Calculators
Molarity Calculator
Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator
Determine the dilution needed to prepare a stock solution.
Reconstitution Calculator
Shall we send you a message when we have discounts available?
Remind me later
Allow
Thank you! Please check your email inbox to confirm.
Oops! Notifications are disabled.
E2325952