Basic information
- CAS
4172-44-5- Standard SMILES
O=C(O)[C@@H](O)[C@H](O)[C@@H](O)CO- InChIKey
QXKAIJAYHKCRRA-NUNKFHFFSA-N- Molecular formula
- C5H10O6
- Average molar mass
- 166.13 g/mol
Overview
L-xylonic acid is a xylonic acid. It is a conjugate acid of a L-xylonate. It is an enantiomer of a D-xylonic acid.
Names & identifiers
- Preferred name
- Xylonic acid, L-
- IUPAC
- (2S,3R,4S)-2,3,4,5-tetrahydroxypentanoic acid
- English name
- L-Xylonic acid
- Molecular formula
- C5H10O6
- Molecular weight
- 166.1293
Names & synonyms
L-xylonic acidXylonic acid, L-LAO7LF939B(2S,3R,4S)-2,3,4,5-tetrahydroxypentanoic acid4172-44-5CHEBI:48092RefChem:151983GlyTouCan:G41308FSG41308FSUNII-LAO7LF939BSCHEMBL13219455QXKAIJAYHKCRRA-NUNKFHFFSA-N
Show more names
L-Xylonic acid lithium salt
C05411L-Xylonic acid lithium salt, >=95.0% (TLC)Q27104604
Database identifiers
- CAS
4172-44-5- PubChem CID
- 6971043
- ChEBI
CHEBI:48092- UNII
- LAO7LF939B
- Nikkaji
- J2.367.490D
Properties
Computed structural properties
- XLogP
- -2.7
- Topological polar surface area
- 118 Ų
- Hydrogen bond donors
- 5
- Hydrogen bond acceptors
- 6
- Rotatable bonds
- 4
- Heavy atoms
- 11
- Formal charge
- 0
- Complexity
- 135
Physicochemical properties
- storage temp.
- 2 · 2-8°C
- form
- solid
- color
- white
- optical activity
- -18 · [α]/D -18±2°, c =1 in H2O
- InChI
- 1S/C5H10O6/c6-1-2(7)3(8)4(9)5(10)11/h2-4,6-9H,1H2,(H,10,11)/t2-,3+,4-/m0/s1
- InChIKey
- QXKAIJAYHKCRRA-NUNKFHFFSA-N
- SMILES
- OC[C@H](O)[C@@H](O)[C@H](O)C(O)=O || OC[C@H](O)[C@@H](O)[C@H](O)C(O)=O
- FDA UNII
- 7 LF939B · LAO7LF939B
- UNSPSC Code
- 12352106 · 12352106
- NACRES
- 25 · NA.25
- WGK Germany
- 3 · WGK 3
- Storage Class
- 11 · 11 - Combustible Solids
Safety & regulation
Safety data
- wgk
- WGK 3
- Storage Class
- 11 - Combustible Solids
Chemistry & industry
Suppliers2 total
西格玛奥德里奇（上海）贸易有限公司21-20338288 · [email protected]
上海梅凯科技有限公司15300790979 18964014359 · [email protected]
Additional notes
DefinitionChEBI: L-xylonic acid is a xylonic acid. It is a conjugate acid of a L-xylonate. It is an enantiomer of a D-xylonic acid.
Related reactions
1 records
Compound notes
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