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D5899

2-Deoxy-D-ribose

BioReagent, suitable for cell culture

Synonym(s):

2-Deoxy-D-arabinose, 2-Deoxy-D-erythropentose, Thyminose

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About This Item

Empirical Formula (Hill Notation):
C5H10O4
CAS Number:
533-67-5
Molecular Weight:
134.13
UNSPSC Code:
12352201
NACRES:
NA.75
PubChem Substance ID:
24893979
EC Number:
208-573-0
Beilstein/REAXYS Number:
1721978
MDL number:
MFCD00135904
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biological source

synthetic (organic)

Quality Level

200

product line

BioReagent

assay

≥99% (GC)

form

powder

technique(s)

cell culture | mammalian: suitable

mp

89-90 °C (lit.)

solubility

water: 100 mg/mL, clear to slightly hazy, colorless to light yellow

storage temp.

2-8°C

SMILES string

OC[C@@H](O)[C@@H](O)CC=O

InChI

1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1

InChI key

ASJSAQIRZKANQN-CRCLSJGQSA-N

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This Item
31170D3179121649
2-Deoxy-D-ribose BioReagent, suitable for cell culture

Sigma-Aldrich

D5899

2-Deoxy-D-ribose

2-Deoxy-D-ribose ≥99.0% (TLC)

Sigma-Aldrich

31170

2-Deoxy-D-ribose

2-Deoxy-D-glucose ≥98% (GC), BioXtra

Sigma-Aldrich

D3179

2-Deoxy-D-glucose

2-Deoxy-D-ribose 97% (GC)

Sigma-Aldrich

121649

2-Deoxy-D-ribose

technique(s)

cell culture | mammalian: suitable

technique(s)

-

technique(s)

gas chromatography (GC): suitable

technique(s)

-

assay

≥99% (GC)

assay

≥99.0% (TLC)

assay

≥98% (GC)

assay

97% (GC)

biological source

synthetic (organic)

biological source

-

biological source

synthetic (organic)

biological source

-

solubility

water: 100 mg/mL, clear to slightly hazy, colorless to light yellow

solubility

water: 50 mg/mL, clear, colorless to faintly yellow

solubility

H2O: 1 M at 20 °C, clear, colorless

solubility

-

form

powder

form

solid

form

powder

form

powder

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

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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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Certificates of Analysis (COA)

Lot/Batch Number
0000558071
0000558071
0000508001
0000508001
0000497753

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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
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
View All Related Papers

Global Trade Item Number

SKUGTIN
D5899-10MG04061833586983
D5899-1G04061833586990

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