G7134
L-(−)-Galactose
≥99% (HPLC)
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About This Item
Fórmula empírica (notación de Hill):
C6H12O6
Número de CAS:
Peso molecular:
180.16
Beilstein/REAXYS Number:
1724622
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
Productos recomendados
Quality Level
assay
≥99% (HPLC)
form
powder
technique(s)
HPLC: suitable
color
white
solubility
water: 50 mg/mL, clear, colorless
SMILES string
OC[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O
InChI
1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3+,4+,5-,6?/m0/s1
InChI key
WQZGKKKJIJFFOK-DHVFOXMCSA-N
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Biochem/physiol Actions
L-Galactose was shown to be a key intermediate in the molecular pathway of converting D-glucose to oxalic acid in Pistia stratiotes.
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Phytochemistry, 53(4), 433-440 (2000-03-24)
Axenic Pistia stratiotes L. plants were pulse-chase labeled with [14C]oxalic acid, L[1-14C]ascorbic acid, L-6-14C]ascorbic acid, D-[1-14C]erythorbic acid, L-[1-14C]galactose, or [1-14C]glycolate. Specific radioactivities of L-ascorbic acid (AsA), free oxalic acid (OxA) and calcium oxalate (CaOx) in labeled plants were compared. Samples
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