L-(+)-threose
Names
[ CAS No. ]:
95-44-3
[ Name ]:
L-(+)-threose
[Synonym ]:
DL-Erythrose
L-Threofuranose
Threose
EINECS 202-419-6
L-Threose
MFCD00066540
(2R,3S)-2,3,4-trihydroxybutanal
UNII-MHH79K1BVR
Threose,L
L-threo-tetrose
Biological Activity
[Description]:
[Related Catalog]:
Chemical & Physical Properties
[ Density]:
1.698g/cm3
[ Boiling Point ]:
290.6ºC at 760mmHg
[ Melting Point ]:
162-163℃
[ Molecular Formula ]:
C4H8O4
[ Molecular Weight ]:
120.10400
[ Flash Point ]:
129.5ºC
[ Exact Mass ]:
120.04200
[ PSA ]:
69.92000
[ Index of Refraction ]:
1.619
MSDS
Safety Information
[ Personal Protective Equipment ]:
Eyeshields;Gloves
[ 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%
Articles
Curr. Protoc. Nucleic Acid Chem. Chapter 4 , Unit 4.54, (2013)
This unit describes the chemical synthesis of α-L-threofuranosyl nucleic acid (TNA) triphosphates for thymidine (T), guanosine (G), cytidine (C), and the diaminopurine (D) analog of adenosine and thei...
The silicate-mediated formose reaction: bottom-up synthesis of sugar silicates.Science 327(5968) , 984-6, (2010)
Understanding the mechanism of sugar formation and stabilization is important for constraining theories on the abiotic origin of complex biomolecules. Although previous studies have produced sugars fr...
Formation of furan and methylfuran from ascorbic acid in model systems and food.Food Addit. Contam. 24 Suppl 1 , 122-35, (2007)
Previous model studies have suggested ascorbic acid as one of the major sources of furan, a possibly hazardous compound found in thermally processed foods (e.g. canned products, jars). The study showe...