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About This Item
Empirical Formula (Hill Notation):
C4H8O4
CAS Number:
Molecular Weight:
120.10
Beilstein:
1721696
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
Recommended Products
form
syrup
Quality Level
optical activity
[α]20/D -16.4 to -9.8 °, c = 2% (w/v) in water
concentration
≥60%
storage temp.
2-8°C
SMILES string
O[C@H]1COC(O)[C@@H]1O
InChI
1S/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2-,3+,4?/m0/s1
InChI key
FMAORJIQYMIRHF-URORKIPUSA-N
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Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Allen Horhota et al.
Journal of the American Chemical Society, 127(20), 7427-7434 (2005-05-19)
alpha-l-Threofuranosyl nucleoside triphosphates (tNTPs) are tetrafuranose nucleoside derivatives and potential progenitors of present-day beta-d-2'-deoxyribofuranosyl nucleoside triphosphates (dNTPs). Therminator DNA polymerase, a variant of the 9 degrees N DNA polymerase, is an efficient DNA-directed threosyl nucleic acid (TNA) polymerase. Here we
Paul Slusarewicz et al.
Journal of materials science. Materials in medicine, 21(4), 1175-1181 (2010-01-14)
We have characterized the relative efficacies of a number of protein crosslinking agents that have the potential for use in the crosslinking of proteinaceous matrices both in vitro and in vivo. The crosslinkers tested were; L: -threose (LT), Genipin (GP)
Hanyang Yu et al.
Nature chemistry, 4(3), 183-187 (2012-02-23)
The pre-RNA world hypothesis postulates that RNA was preceded in the evolution of life by a simpler genetic material, but it is not known if such systems can fold into structures capable of eliciting a desired function. Presumably, whatever chemistry
Diogo R B Ducatti et al.
Organic & biomolecular chemistry, 7(9), 1980-1986 (2009-07-11)
The Hantzsch reaction of C-glycosyl aldehyde/enamino ester/beta-ketoester systems under l-proline catalysis to give dihydropyridine C-glycoconjugates is reported. Asymmetric cyclocondensations of differentially substituted enamine and beta-dicarbonyl components with formyl alpha-L-C-threofuranoside and with the alpha-D-isomer were also carried out. Each reaction occurred
Carine Chevrier et al.
Bioorganic & medicinal chemistry, 15(12), 4125-4135 (2007-04-17)
Cyclic D- and L-4-aminothreose were synthesised from ethyl D- and L-tartrate, respectively. D-aminothreose was a potent inhibitor of alpha-glucosidase and of alpha-mannosidase. From the glycosidase inhibition potencies of the four 4-amino-4-deoxy-tetroses, the contribution of binding of each functionality of the
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