WARNING: This product is for research use only, not for human or veterinary use.
MedKoo CAT#: 530809
Description: alpha-D-Lyxofuranose is a bioactive chemical.
MedKoo Cat#: 530809
Chemical Formula: C5H10O5
Exact Mass: 150.0528
Molecular Weight: 150.13
Elemental Analysis: C, 40.00; H, 6.71; O, 53.28
This product is not in stock, which may be available by custom synthesis.
For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge).
Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.
IUPAC/Chemical Name: alpha-D-Lyxofuranose
InChi Key: HMFHBZSHGGEWLO-STGXQOJASA-N
InChi Code: InChI=1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3+,4+,5+/m1/s1
SMILES Code: O[C@@H]1[C@H]([C@H]([C@@H](CO)O1)O)O
Appearance: Solid powder
Purity: >98% (or refer to the Certificate of Analysis)
Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility: Soluble in DMSO
Shelf Life: >3 years if stored properly
Drug Formulation: This drug may be formulated in DMSO
Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code: 2934.99.9001
The following data is based on the product molecular weight 150.13 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
|Concentration / Solvent Volume / Mass||1 mg||5 mg||10 mg|
|1 mM||1.15 mL||5.76 mL||11.51 mL|
|5 mM||0.23 mL||1.15 mL||2.3 mL|
|10 mM||0.12 mL||0.58 mL||1.15 mL|
|50 mM||0.02 mL||0.12 mL||0.23 mL|
1: Prasad Mishra G, Venkata Ramana G, Venkateswara Rao B. Synthesis of 4a-carba-alpha-D-lyxofuranose from 2,3-O-isopropylidene-L-erythruronolactone via Tebbe-mediated cascade reaction. Chem Commun (Camb). 2008 Aug 7;(29):3423-5. doi: 10.1039/b802418a. Epub 2008 May 21. PubMed PMID: 18633510.
2: Taubert S, Konschin H, Sundholm D. Computational studies of 13C NMR chemical shifts of saccharides. Phys Chem Chem Phys. 2005 Jul 7;7(13):2561-9. Epub 2005 Jun 9. PubMed PMID: 16189565.
3: Claridge TD, Long DD, Baker CM, Odell B, Grant GH, Edwards AA, Tranter GE, Fleet GW, Smith MD. Helix-forming carbohydrate amino acids. J Org Chem. 2005 Mar 18;70(6):2082-90. PubMed PMID: 15760191.
4: Gosselin G, Bergogne MC, De Rudder J, De Clercq E, Imbach JL. Systematic synthesis and biological evaluation of alpha- and beta-D-lyxofuranosyl nucleosides of the five naturally occurring nucleic acid bases. J Med Chem. 1987 Jun;30(6):982-91. PubMed PMID: 3585910.