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2-Deoxy-D-Ribose - 98%, high purity , CAS No.533-67-5

11 Citations

COA

Grade & Purity:

≥98%

Cas Number: 533-67-5
Molecular Weight: 134.13
Beilstein Registry Number: 1721978
EC Number: 208-573-0
MDL number: MFCD00135904
PubChem CID: 5460005

In stock

Item Number

D104784

Grouped product items
SKU	Size	Availability	Price
D104784-1g	1g	3	$9.90
D104784-5g	5g	3	$27.90
D104784-25g	25g	2	$82.90
D104784-100g	100g	2	$297.90
D104784-500g	500g	3	$1,338.90

Endothelial-cell chemoattractant and angiogenesis-inducing factor.

View related series

Chemical Biology (1255) Metabolite (5307) monosaccharide (323)

Basic Description

Synonyms	2-Deoxy-D-ribose, 97% \| CHEBI:28816 \| NSC-772796 \| ASJSAQIRZKANQN-CRCLSJGQSA-N \| BBL012499 \| 2-Deoxy-D-ribose \| 2-Deoxy-D-ribose, >=99.0% (TLC) \| AM20100306 \| 4-01-00-04181 (Beilstein Handbook Reference) \| aldehydo-2-deoxy-D-ribose \| D-erythro-Pentose, 2-
Specifications & Purity	≥98%
Biochemical and Physiological Mechanisms	Reducing sugar used to study processes of oxidative stress and glycation in vivo and in vitro . Induces apoptosis by inhibiting the synthesis and increasing the efflux of glutathione. Endothelial-cell chemoattractant and angiogenesis-inducing factor
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Note	Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic oxygen compounds
  - Class Organooxygen compounds
    - Subclass Carbonyl compounds
      - Level5 Aldehydes
        Level6 Beta-hydroxy aldehydes

Kingdom	Organic compounds
Superclass	Organic oxygen compounds
Class	Organooxygen compounds
Subclass	Carbonyl compounds
Intermediate Tree Nodes	Aldehydes
Direct Parent	Beta-hydroxy aldehydes
Alternative Parents	Alpha-hydrogen aldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
Molecular Framework	Aliphatic acyclic compounds
Substituents	Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Alcohol - Aliphatic acyclic compound
Description	This compound belongs to the class of organic compounds known as beta-hydroxy aldehydes. These are organic compounds containing an aldehyde substituted with a hydroxy group on the second carbon atom.
External Descriptors	deoxypentose
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	(3S,4R)-3,4,5-trihydroxypentanal
INCHI	InChI=1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1
InChIKey	ASJSAQIRZKANQN-CRCLSJGQSA-N
Smiles	C(C=O)C(C(CO)O)O
Isomeric SMILES	C(C=O)[C@@H]([C@@H](CO)O)O
WGK Germany	3
RTECS	SB7230000
Molecular Weight	134.13
Beilstein	1721978
Reaxy-Rn	1904591
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904591&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

10 results found

Lot Number	Certificate Type	Date	Item
A2115191	Certificate of Analysis	Nov 04, 2024	D104784
C1526014	Certificate of Analysis	Nov 11, 2022	D104784
E1802055	Certificate of Analysis	Mar 30, 2022	D104784
E1802054	Certificate of Analysis	Mar 30, 2022	D104784
D2408067	Certificate of Analysis	Mar 04, 2022	D104784
L2216811	Certificate of Analysis	Mar 04, 2022	D104784
F2208081	Certificate of Analysis	Mar 04, 2022	D104784
F2208274	Certificate of Analysis	Mar 04, 2022	D104784
F2208088	Certificate of Analysis	Mar 04, 2022	D104784
F2208087	Certificate of Analysis	Mar 04, 2022	D104784

Chemical and Physical Properties

Solubility	Soluble in water.
Sensitivity	Hygroscopic
Specific Rotation[α]	-56 ° (C=1, H2O)
Melt Point(°C)	91°C
Molecular Weight	134.130 g/mol
XLogP3	-2.300
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	4
Exact Mass	134.058 Da
Monoisotopic Mass	134.058 Da
Topological Polar Surface Area	77.800 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	83.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	2
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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