2-DEOXY-D-ARA­BI­NOSE CAS 533-67-5

• Iden­ti­fi­ca­tion
• Prop­er­ties
• Safe­ty Data
• Spec­i­fi­ca­tions & Oth­er Information
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Iden­ti­fi­ca­tion

CAS Number

533-67-5

Name

2-DEOXY-D-ARA­BI­NOSE

Syn­onyms

(3S,4R)-3,4,5-Trihydroxypentanal

1724-14-7

[RN]
2-Deoxy-D-ara­bi­nose

2-Deoxy-D-ery­thro-pen­­tose

[IUPAC name – gen­er­at­ed by ACD/​Name]
2-Deoxy-D-ery­thropen­­tose

2-Deoxy-D-Ribose

2-Deoxy-β-D-ery­thro-pen­­tose

2-deoxyri­­bose

2-Des­oxy-D-ery­thro-pen­­tose

[Ger­man]

[IUPAC name – gen­er­at­ed by ACD/​Name]
2-Désoxy-D-éry­thro-pen­­tose

[French]

[IUPAC name – gen­er­at­ed by ACD/​Name]
217-028-6

[EINECS]
533-67-5

[RN]
D-2-Deox­­yara­bi­nose

D-2-Deoxyri­­bose

D-2-RIBODES­OSE

D-erylhro-2-Deoxypen­­tose

D-ery­thro-Pen­­tose, 2-deoxy-

[IUPAC index name – gen­er­at­ed by ACD/​Name]
D-Ribose, 2-deoxy-

Deoxyri­bose

[Wiki]
des­oxyri­bose

LSW4H01241

[UNII]
Thymi­nose

SMILES

O=CCC@HC@HCO

Std­InChI

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

Std­InChIKey

ASJSAQIRZKAN­QN-CRCLSJGQSA-N

Mol­e­c­u­lar Formula

C5H10O4

Mol­e­c­u­lar Weight

134.131

EINECS

208-573-0

Beil­stein Reg­istry Number

1721978

MDL Number

MFCD00135904

Prop­er­ties

Appear­ance

White to off-white crys­talline powder

Safe­ty Data

Sym­bol

Sig­nal Word

WGK Germany

3

MSDS Download

Spec­i­fi­ca­tions and Oth­er Infor­ma­tion of Our 2-DEOXY-D-ARA­BI­NOSE CAS 533-67-5

Iden­ti­fi­ca­tion Methods

HPLC

Puri­ty

98% min

Rota­tion

-54° ~ -60°

Heavy Met­als

≤10ppm

PH

6.0 ~8.0

Loss on Drying

≤1.0%

Residue on Ignition

≤0.5%

Shelf Life

2 years

Stor­age

Under room tem­per­a­ture away from light

Known Appli­ca­tion

2-Deoxy-D-ribose is wide­ly used in DNA research, cell oxida­tive stress exper­i­ments, bio­chem­i­cal analy­sis, and nucle­o­side syn­the­sis. It is not a prod­uct with direct indus­tri­al or phar­ma­ceu­ti­cal appli­ca­tions. Main Appli­ca­tions 1. Research Uses As a basic build­ing block of DNA, it is often used in mol­e­c­u­lar biol­o­gy research. The metab­o­lism and role of 2-deoxy-D-ribose are often explored in stud­ies of DNA dam­age and repair mech­a­nisms. 2. Bio­chem­i­cal Reagents It is often used as a reduc­ing sug­ar in bio­chem­i­cal exper­i­ments, such as test­ing redox reac­tions and free rad­i­cal reac­tions. It is used in detec­tion and quan­tifi­ca­tion meth­ods (for exam­ple, deter­min­ing the con­tent of deoxy­sug­ars). 3. Med­ical and Phar­ma­co­log­i­cal Research It is used as an induc­ing fac­tor in cell oxida­tive stress and apop­to­sis exper­i­ments because it pro­motes the gen­er­a­tion of reac­tive oxy­gen species (ROS). Stud­ies have used it to inves­ti­gate the mech­a­nisms of oxida­tive stress asso­ci­at­ed with car­dio­vas­cu­lar dis­ease, dia­bet­ic com­pli­ca­tions, and oth­er con­di­tions. 4. Syn­thet­ic Appli­ca­tions It can serve as an inter­me­di­ate in the syn­the­sis of cer­tain nucle­o­sides, nucleotides, or nucle­o­side analogs.

Gen­er­al View of Documents

Links

This prod­uct is devel­oped by our R&D com­pa­ny Cam­ing Phar­ma­ceu­ti­cal Lim­it­ed (http://​www​.cam​ing​.com/).

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