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24259-59-4

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  • L-Ribose/ carbonhydrate / Intermediate/white powder with cas no. 24259-59-4/ worldwide Top Pharma factory vendor with most competitive price

    Cas No: 24259-59-4

  • USD $ 540.0-600.0 / Kilogram

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24259-59-4 Usage

Description

Ribose is a monosaccharide, specifically a five-carbon sugar with the chemical formula C5H10O5. It is rarely found free in nature but is crucial as a component of RNA (ribonucleic acid). Its derivative, deoxyribose (C5H10O4), is also significant as a constituent of DNA (deoxyribonucleic acid), which carries the genetic code in chromosomes. Ribose is characterized by its white crystalline or powdery appearance.

Uses

1. Used in Pharmaceutical and Biotechnology Industry:
Ribose is used as a key component in the synthesis of RNA and DNA for various applications in the pharmaceutical and biotechnology industries. It plays a vital role in the development of drugs targeting genetic disorders and the study of genetic mechanisms.
2. Used in Organic Synthesis:
L-[1-13C]ribose is a compound used in organic synthesis, which is essential for the development of new chemical compounds and materials with specific properties and applications.
3. Used in Research and Diagnostics:
Ribose is utilized in research and diagnostics, particularly in the study of RNA and DNA structures, functions, and interactions. It is also used in the development of diagnostic tools and techniques for genetic and molecular biology research.
4. Used in Nutritional Supplements:
Ribose is used as an ingredient in nutritional supplements, particularly for athletes and individuals recovering from intense physical activity. It aids in the production of adenosine triphosphate (ATP), which is essential for energy production in cells.
5. Used in Food Industry:
Ribose is employed in the food industry as a natural flavor enhancer and sweetener due to its sugar-like properties.
6. Produced by Microorganism Fermentation:
Ribose is produced through the fermentation of glucose by microorganisms in a fermentation culture medium without the addition of calcium carbonate. This method is used to obtain ribose for various industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 24259-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24259-59:
(7*2)+(6*4)+(5*2)+(4*5)+(3*9)+(2*5)+(1*9)=114
114 % 10 = 4
So 24259-59-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4-,5+/m0/s1

24259-59-4 Well-known Company Product Price

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  • TCI America

  • (R0068)  L-Ribose  >98.0%(HPLC)

  • 24259-59-4

  • 1g

  • 360.00CNY

  • Detail
  • TCI America

  • (R0068)  L-Ribose  >98.0%(HPLC)

  • 24259-59-4

  • 5g

  • 890.00CNY

  • Detail
  • TCI America

  • (R0068)  L-Ribose  >98.0%(HPLC)

  • 24259-59-4

  • 25g

  • 2,890.00CNY

  • Detail
  • Alfa Aesar

  • (B21117)  L-(+)-Ribose, 99%   

  • 24259-59-4

  • 250mg

  • 613.0CNY

  • Detail
  • Alfa Aesar

  • (B21117)  L-(+)-Ribose, 99%   

  • 24259-59-4

  • 1g

  • 1901.0CNY

  • Detail
  • Alfa Aesar

  • (B21117)  L-(+)-Ribose, 99%   

  • 24259-59-4

  • 5g

  • 7650.0CNY

  • Detail
  • Alfa Aesar

  • (B21117)  L-(+)-Ribose, 99%   

  • 24259-59-4

  • 25g

  • 26778.0CNY

  • Detail

24259-59-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name aldehydo-L-ribose

1.2 Other means of identification

Product number -
Other names 6-Deoxy-D-altrose

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24259-59-4 SDS

24259-59-4Relevant articles and documents

A new oleanane-type triterpenoidal saponin from Pulsatilla chinensis

Shu, Zhan,Chen, Zhong,Liu, Yan-Li,Zhu, Wei-Feng,Feng, Yu-Lin,Xu, Qiong-Ming,Li, Xiao-Ran,Yang, Shi-Lin

, p. 2196 - 2201 (2013)

A new oleanane-type triterpenoidal saponin, 3-O-β-d-glucopyranosyl- hederagenin 23-O-α-d-ribofuranoside (1), was isolated from the roots of Pulsatilla chinensis, and its structure was established on the basis of the spectral data. Compounds 2, 7 and 8 showed moderate cytotoxic activity by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazoliumbromide assay. 2013

NAD(P)H oxidase v from Lactobacillus plantarum (NoxV) displays enhanced operational stability even in absence of reducing agents

Park, Jonathan T.,Hirano, Jun-Ichiro,Thangavel, Vaijayanthi,Riebel, Bettina R.,Bommarius, Andreas S.

, p. 159 - 165 (2011)

Active pharmaceutical ingredients (APIs) such as l-sugars and keto acids are favorably accessed through selective oxidation of sugar alcohols and amino acids, respectively, catalyzed by NAD(P)-dependent dehydrogenases. Cofactor regeneration from NAD(P)H conveniently is achieved via water-forming NAD(P)H oxidases (nox2), which only need molecular oxygen as co-substrate. Turnover-dependent overoxidation of the conserved cysteine residue in the active site of water-forming NADH oxidases is the presumed cause of the limited nox2 stability. We present a novel NAD(P)H oxidase, NoxV from Lactobacillus plantarum, with specific activity of 167 U/mg and apparent kinetic constants at air saturation and 25 °C of kcat,app = 212 s-1 and KM,app = 50.2 μM in the broad pH optimum from 5.5 to 8.0. The enzyme features a higher stability than other NAD(P)H oxidases against overoxidation, as is evidenced by a higher total turnover number, in the presence (168,000) and, most importantly, also in the absence (128,000) of exogenously added reducing agents. While the native enzyme shows exclusively activity on NADH, we engineered the substrate binding pocket to generate variants, G178K,R and L179K,R,H that accommodate and oxidize both NADH and NADPH as substrates.

A heterogeneous Pd-Bi/C catalyst in the synthesis of l-lyxose and l-ribose from naturally occurring d-sugars

Fan, Ao,Jaenicke, Stephan,Chuah, Gaik-Khuan

supporting information; experimental part, p. 7720 - 7726 (2011/12/04)

A critical step in the synthesis of the rare sugars, l-lyxose and l-ribose, from the corresponding d-sugars is the oxidation to the lactone. Instead of conventional oxidizing agents like bromine or pyridinium dichromate, it was found that a heterogeneous catalyst, Pd-Bi/C, could be used for the direct oxidation with molecular oxygen. The composition of the catalyst was optimized and the best results were obtained with 5:1 atomic ratio of Pd:Bi. The overall yields of the five-step procedure to l-ribose and l-lyxose were 47% and 50%, respectively. The synthetic procedure is advantageous from the viewpoint of overall yield, reduced number of steps, and mild reaction conditions. Furthermore, the heterogeneous oxidation catalyst can be easily separated from the reaction mixture and reused with no loss of activity.

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