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About This Item
Empirical Formula (Hill Notation):
C5H11O7P · 2C6H13N
CAS Number:
Molecular Weight:
412.46
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
Beilstein/REAXYS Number:
3785872
biological source
synthetic (organic)
Quality Segment
assay
≥97% (TLC)
form
powder
color
white
solubility
water: 50 g/L at 20 °C
storage temp.
−20°C
SMILES string
NC1CCCCC1.NC2CCCCC2.OC[C@H]3O[C@@H](C[C@@H]3O)OP(O)(O)=O
InChI
1S/2C6H13N.C5H11O7P/c2*7-6-4-2-1-3-5-6;6-2-4-3(7)1-5(11-4)12-13(8,9)10/h2*6H,1-5,7H2;3-7H,1-2H2,(H2,8,9,10)/t;;3-,4+,5+/m..0/s1
InChI key
GVYUZZDUVZHJAM-CGKAESPRSA-N
Application
2-Deoxyribose 1-phosphate (2dR1P) may be used in pyrimidine metabolism research to identify and characterize thymidine phosphorylase(s)/platelet-derived endothelial cell growth factor(s)(PD-ECGF)/gliostatin(s). 2-Deoxyribose 1-phosphate may be used to study processes such as angiogenesis in tumor cells at the level of thymidine phosphorylase activity. 2-Deoxy-a-D-ribose 1-phosphate (dR-1-P) is used in the organic synthesis of 2′-deoxynucleosides such as cladribine.
Preparation Note
Enzymatically prepared
Other Notes
To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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