Unfortunately, this product is not tested for heavy metals. Currently, there is no product option available that included heavy metal testing.
121649
2-Deoxy-D-ribose
97% (GC)
2-Deoxy-D-ribose
Synonim(y):
2-Deoxy-D-arabinose, 2-Deoxy-D-erythropentose, Thyminose
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1 G
103,00 zł
5 G
296,65 zł
25 G
788,80 zł
103,00 zł
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C5H10O4
Numer CAS:
Masa cząsteczkowa:
134.13
UNSPSC Code:
12352201
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-573-0
Beilstein/REAXYS Number:
1721978
MDL number:
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Pozwól nam pomócNazwa produktu
2-Deoxy-D-ribose, 97% (GC)
InChI key
ASJSAQIRZKANQN-CRCLSJGQSA-N
InChI
1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1
SMILES string
OC[C@@H](O)[C@@H](O)CC=O
assay
97% (GC)
form
powder
optical activity
[α]22/D −59°, c = 1 in H2O
color
white to off-white
mp
89-90 °C (lit.)
Quality Level
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Ta pozycja | 31170 | D5899 | D3179 |
|---|---|---|---|
| assay 97% (GC) | assay ≥99.0% (TLC) | assay ≥99% (GC) | assay ≥98% (GC) |
| Quality Level 100 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
| form powder | form solid | form powder | form powder |
| color white to off-white | color white | color - | color white |
| mp 89-90 °C (lit.) | mp 89-90 °C (lit.) | mp 89-90 °C (lit.) | mp 146-147 °C (lit.) |
| optical activity [α]22/D −59°, c = 1 in H2O | optical activity [α]20/D −56±2°, 24 hr, c = 1% in H2O | optical activity - | optical activity - |
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.
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Klasa składowania
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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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Tymofii Yu Nikolaienko et al.
Physical chemistry chemical physics : PCCP, 14(44), 15554-15561 (2012-10-18)
Relaxed force constants (RFC) and vibrational root-mean-square (VRMS) deviations are used for comparative characterization of mechanical properties of canonical 2'-deoxyribonucleosides (2DRs) and 1,2-dideoxyribose molecule, their model sugar residue. It has been shown that RFC and VRMS should be preferred over
Anita R Peoples et al.
Nucleic acids research, 40(13), 6060-6069 (2012-04-03)
Our mechanistic understanding of damage formation in DNA by the direct effect relies heavily on what is known of free radical intermediates studied by EPR spectroscopy. Bridging this information to stable product formation requires methods with comparable sensitivities, a criterion
Manuel Ellermann et al.
Acta crystallographica. Section D, Biological crystallography, 68(Pt 3), 253-260 (2012-02-22)
The biological activity of catechol neurotransmitters such as dopamine in the synapse is modulated by transporters and enzymes. Catechol-O-methyltransferase (COMT; EC 2.1.1.6) inactivates neurotransmitters by catalyzing the transfer of a methyl group from S-adenosylmethionine to catechols in the presence of
Waseem Hassan et al.
Chemico-biological interactions, 199(2), 96-105 (2012-06-12)
The study was designed to explore the biochemical influence of non bonding nitrogen interactions (N⋯Se/S) on organochalcogens potency. Approximately five and six times higher thiol peroxidase (TPx) like activity was observed for compound (C)-2 than C-1 and C-3, respectively. C-2
Buthina Al-Oudat et al.
Bioorganic & medicinal chemistry letters, 23(3), 854-859 (2012-12-26)
Well-defined substrates for the study of oxidative processes are important for the elucidation of the role of DNA damage in the etiology of diseases such as cancer. We have synthesized 3'-modified oligodeoxyribonucleotides (ODNs) using 5'→3' 'reverse' DNA synthesis for the
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