L-Xylose - CAS 609-06-3

Catalog:	BB030853
Product Name:	L-Xylose
CAS:	609-06-3
Synonyms:	Xylose, L-; NSC 26213

Technical Data

Safety and Hazards

Patents

Literatures

Computed Properties

IUPAC Name:	(2S,3R,4S)-2,3,4,5-tetrahydroxypentanal
Description:	L-Xylose is used as a selective sodium-dependent glucose cotransporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes.
Molecular Weight:	150.13
Molecular Formula:	C5H10O5
Canonical SMILES:	C(C(C(C(C=O)O)O)O)O
InChI:	InChI=1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5+/m1/s1
InChI Key:	PYMYPHUHKUWMLA-WISUUJSJSA-N
Boiling Point:	415.5±38.0°C at 760 mmHg
Melting Point:	144°C
Density:	1.508±0.06 g/cm3
LogP:	-2.73970

Publication Number	Title	Priority Date
CN-113502249-A	Bacillus amyloliquefaciens HTGC-10 and fermentation application method thereof for producing beta-mannase	20210728
CN-113463388-A	Inorganic/polymer composite membrane for preventive protection of paper cultural relics and preparation method thereof	20210720
CN-113430135-A	Lactobacillus helveticus strain with depression improving effect and application thereof	20210701
KR-102294437-B1	Infant and child origin lactic acid bacteria Lactobacillus plantarum MG4553 and composition comprising the lactic acid bacteria for enhancing intestine activity, anti-oxidant and anti-obesity	20210217
KR-102294442-B1	Infant and child origin lactic acid bacteria Lactobacillus plantarum MG4555 and composition comprising the lactic acid bacteria for enhancing intestine activity, anti-oxidant and anti-obesity	20210217

PMID	Publication Date	Title	Journal
22840047	20121001	A polysaccharide from Sargassum fusiforme protects against immunosuppression in cyclophosphamide-treated mice	Carbohydrate polymers
22058322	20120901	Enterococcus rivorum sp. nov., from water of pristine brooks	International journal of systematic and evolutionary microbiology
22532020	20120501	Simultaneous determination of the absolute configuration of twelve monosaccharide enantiomers from natural products in a single injection by a UPLC-UV/MS method	Planta medica
22292940	20120217	SmI2-mediated cross-coupling of nitrones with β-silyl acrylates: synthesis of (+)-australine	Organic letters
22133443	20120105	Production of L-xylose from L-xylulose using Escherichia coli L-fucose isomerase	Enzyme and microbial technology

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GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	104
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	3
Defined Bond Stereocenter Count:	0
Exact Mass:	150.05282342
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	5
Hydrogen Bond Donor Count:	4
Isotope Atom Count:	0
Monoisotopic Mass:	150.05282342
Rotatable Bond Count:	4
Topological Polar Surface Area:	98 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	-2.3