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Home > Encyclopedia > L-xylo-hex-2-ulosonic acid

L-xylo-hex-2-ulosonic acid

L-xylo-hex-2-ulosonic acid structure

L-xylo-hex-2-ulosonic acid 

structure
  • CAS No:

    526-98-7

  • Formula:

    C6H10O7

  • Chemical Name:

    L-xylo-hex-2-ulosonic acid

  • Synonyms:

    L-Xylohexulosonic acid;2-Keto-L-gulonsure;2-Oxo-2-deoxy-L-gulonic acid;2-Oxo-L-gulonic acid;L-xylo-2-Hexulosonic acid;3-Keto-L-gulonic acid;Einecs 208-403-5;Idonic acid, 2-keto-, L-

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

2-dehydro-L-idonic acid is a ketoaldonic acid. It derives from a L-idonic acid and a L-gulonic acid. It is a conjugate acid of a 2-dehydro-L-idonate.


Crystallise 2-keto-L-gulonic acid from half its weight of water, wash it with Me2CO and dry it in vacuo. [Reichstein et al. Helv Chim Acta 17 311 1934, NMR: Crawford et al. J Am Chem Soc 102 2220 1980. Beilstein 3 IV 1985.]

L-xylo-hex-2-ulosonic acid Basic Attributes

194.14

194.14

208-403-5

I49386U15C

Off-White to Pale Beige

2918990090

Characteristics

135.29000

-2.9

1.757±0.06 g/cm3(Predicted)

171 °C

550.6±50.0 °C(Predicted)

300.9ºC

1.593

335.3g/L at 20℃

0Pa at 25℃

2.10±0.54(Predicted)

Safety Information

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

Drug Information

Precursor forms of vitamins. (See all compounds classified as Provitamins.)

2-keto-L-gulonic acid

L-xylo-hex-2-ulosonic acid Use and Manufacturing

2-Keto-L-gulonic Acid is used in biological studies for the formation of sorbitol metabolism by Acetobacter melanogenus.

Computed Properties

Molecular Weight:194.14
XLogP3:-2.9
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:5
Exact Mass:194.04265265
Monoisotopic Mass:194.04265265
Topological Polar Surface Area:135
Heavy Atom Count:13
Complexity:201
Defined Atom Stereocenter Count:3
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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