L-Gulose

Modify Date: 2024-01-02 11:22:14

L-Gulose Structure
L-Gulose structure
Common Name L-Gulose
CAS Number 6027-89-0 Molecular Weight 180.156
Density 1.7±0.1 g/cm3 Boiling Point 410.8±45.0 °C at 760 mmHg
Molecular Formula C6H12O6 Melting Point 132ºC
MSDS USA Flash Point 202.2±28.7 °C

 Use of L-Gulose


L-Gulose, the putative furanose form of L-sorbosone, is an L-hexose sugar and an intermediate in the biosynthesis of L-Ascorbate (vitamin C)[1].

 Names

Name aldehydo-L-gulose
Synonym More Synonyms

 L-Gulose Biological Activity

Description L-Gulose, the putative furanose form of L-sorbosone, is an L-hexose sugar and an intermediate in the biosynthesis of L-Ascorbate (vitamin C)[1].
Related Catalog
References

[1]. Teruhide Sugisawa, et al. Microbial production of L-ascorbic acid from D-sorbitol, L-sorbose, L-gulose, and L-sorbosone by Ketogulonicigenium vulgare DSM 4025. Biosci Biotechnol Biochem. 2005 Mar;69(3):659-62.

 Chemical & Physical Properties

Density 1.7±0.1 g/cm3
Boiling Point 410.8±45.0 °C at 760 mmHg
Melting Point 132ºC
Molecular Formula C6H12O6
Molecular Weight 180.156
Flash Point 202.2±28.7 °C
Exact Mass 180.063385
PSA 118.22000
LogP -1.88
Vapour Pressure 0.0±2.2 mmHg at 25°C
Index of Refraction 1.635
Storage condition 2-8°C

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases 24/25-36/37/39-27-26
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2912491000

 Customs

HS Code 2912491000
Summary 2912491000. other aldehyde-alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles24

More Articles
Preparation of D-gulose from disaccharide lactitol using microbial and chemical methods.

Biosci. Biotechnol. Biochem. 77(2) , 253-8, (2013)

When an M31 strain of Agrobacterium tumefaciens was grown in a mineral salt medium at 30 °C containing 1.0% lactitol as sole carbon source, a keto-sugar was efficiently accumulated in the supernatant....

The role of the gulose-mannose part of bleomycin in activation of iron-molecular oxygen complexes.

Biochem. J. 253(2) , 497-504, (1988)

A comparison of the complexing properties of metal ions and O2 activation by bleomycin-A2 (BLM-A2) and deglyco-BLM-A2 is presented. Deglyco-BLM-A2 is obtained from the parent derivative by HF cleavage...

Regio- and stereo-selective synthesis of carbohydrate isoxazolidines by 1,3-dipolar cycloaddition of nitrones to 5,6-dideoxy-1,2-O-isopropylidene- alpha-D-xylo-hex-5-enofuranose.

Carbohydr. Res. 226(1) , 49-56, (1992)

The synthesis of 2-phenyl-3-aryl and 2-phenyl-3-aroyl derivatives 5-(1,2-O-isopropylidene-alpha-D-xylo-tetrofuranos-4-yl)isoxazolidi ne (3) from nitrones and 5,6-dideoxy-1,2-O-isopropylidene-alpha-D-x...

 Synonyms

EINECS 227-897-3
MFCD00136022
L-(+)-Gulose
L-Gulopyranose
Gulopyranose
Gulose
L-Gulose
β-L-gulose
Top Suppliers:I want be here




Get all suppliers and price by the below link:

L-Gulose suppliers

L-Gulose price