L-(+)-Ribose - ≥98% , CAS No.24259-59-4

CAS: 24259-59-4 Cat. No.: R105972 Peso molecular: 150.13 Beilstein Registry Number: 1723084 Número EC: 246-110-4
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
L-(+)-Ribose | DS-18039 | UNII-ON80XH54BH | PYMYPHUHKUWMLA-MROZADKFSA-N | EINECS 246-110-4 | A817176 | C5H10O5 | ON80XH54BH | AKOS006239066 | O11840 | CHEBI:47015 | aldehydo-L-ribo-pentose | L- masculineEIC | Q27120760 | L-(+)-Ribos | L-Ribose | aldehydo-
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
R105972-1g
5
9,90US$
5g
R105972-5g
3
10,90US$
10g
R105972-10g
3

12,90US$

19,90US$
Guardar 7,00 US$ (35.18%)
25g
R105972-25g
2

31,90US$

47,90US$
Guardar 16,00 US$ (33.40%)
100g
R105972-100g
2

87,90US$

131,90US$
Guardar 44,00 US$ (33.36%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 26 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
L-(+)-Ribose | DS-18039 | UNII-ON80XH54BH | PYMYPHUHKUWMLA-MROZADKFSA-N | EINECS 246-110-4 | A817176 | C5H10O5 | ON80XH54BH | AKOS006239066 | O11840 | CHEBI:47015 | aldehydo-L-ribo-pentose | L- masculineEIC | Q27120760 | L-(+)-Ribos | L-Ribose | aldehydo-
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504756026
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504756026
Sonrisas canónicasC(C(C(C(C=O)O)O)O)O
IUPAC Name(2S,3S,4S)-2,3,4,5-tetrahydroxypentanal
InChIKeyPYMYPHUHKUWMLA-MROZADKFSA-N
INCHI1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5-/m1/s1
Isómeros SMILES C([C@@H]([C@@H]([C@@H](C=O)O)O)O)O
WGK Alemania 3
Peso molecular 150.13
Beilstein 1723084
Reaxy-Rn 2325068
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2325068&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct ParentPentoses
Alternative Parents Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Short-chain aldehydes  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Pentose monosaccharide - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.
External Descriptors aldehydo-ribose - L-ribose
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

19 results found

Lot NumberCertificate TypeFechaArticulo
C1814050Certificate of AnalysisOct 14, 2025 R105972
C1814049Certificate of AnalysisOct 14, 2025 R105972
L2326122Certificate of AnalysisDec 08, 2023 R105972
L2326201Certificate of AnalysisDec 08, 2023 R105972
L2326200Certificate of AnalysisDec 08, 2023 R105972
L2326129Certificate of AnalysisDec 08, 2023 R105972
L2326128Certificate of AnalysisDec 08, 2023 R105972
L2326127Certificate of AnalysisDec 08, 2023 R105972
L2326126Certificate of AnalysisDec 08, 2023 R105972
L2326125Certificate of AnalysisDec 08, 2023 R105972
L2326124Certificate of AnalysisDec 08, 2023 R105972
L2326123Certificate of AnalysisDec 08, 2023 R105972
A2604154Certificate of AnalysisDec 08, 2023 R105972
G2508110Certificate of AnalysisDec 08, 2023 R105972
A2628095Certificate of AnalysisDec 08, 2023 R105972
H2322662Certificate of AnalysisJul 27, 2023 R105972
H2322661Certificate of AnalysisJul 27, 2023 R105972
H2322633Certificate of AnalysisJul 27, 2023 R105972
E2323054Certificate of AnalysisNov 03, 2021 R105972

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Propiedades químicas y físicas
SolubilidadSoluble in water (100 mg/ml).
SensibilidadMoisture sensitive
Rotación específica [α]20 ° (C=1, H2O)
Punto de fusión (°C)90°C
Peso molecular150.130 g/mol
XLogP3-2.300
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass150.053 Da
Monoisotopic Mass150.053 Da
Topological Polar Surface Area98.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity104.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Zheng Qian, Long Si, Chen Zhi, Fu Jiaolong, Ju Xin, Li Liangzhi.  (2023)  Characterization of a novel ribose-5-phosphate isomerase B from Curtobacterium flaccumfaciens ZXL1 for D-allose production.  FOOD SCIENCE AND BIOTECHNOLOGY,      [PMID:38623425] [10.1007/s10068-023-01457-0]
2. Yang Liu, Limei Ran, Yahong Wang, Peng Wan, Hongli Zhou.  (2023)  Basic characterization, antioxidant and immunomodulatory activities of polysaccharides from sea buckthorn leaves.  FITOTERAPIA,      [PMID:37343686] [10.1016/j.fitote.2023.105592]
3. Hao Tang, Jinwen Huang, Qingxia Yuan, Kunling Lv, Haiqiong Ma, Tingting Li, Yonghong Liu, Shunli Mi, Longyan Zhao.  (2023)  A regular Chlorella mannogalactan and its sulfated derivative as a promising anticoagulant: Structural characterization and anticoagulant activity.  CARBOHYDRATE POLYMERS,      [PMID:37173047] [10.1016/j.carbpol.2023.120956]
4. Yaxian Chen, Yini Cai, Zhimin Zhao, Depo Yang, Xinjun Xu.  (2023)  Optimization of Extraction Process, Preliminary Characterization and Safety Study of Crude Polysaccharides from Morindae Officinalis Radix.  Foods,  12  (8): (1590).  [PMID:37107385] [10.3390/foods12081590]
5. Zhengyu Hu, Jiaming Wang, Long Jin, Tieqiang Zong, Yuanqi Duan, Jinfeng Sun, Wei Zhou, Gao Li.  (2022)  Preparation, Characterization and Anti-Complementary Activity of Three Novel Polysaccharides from Cordyceps militaris.  Polymers,  14  (21): (4636).  [PMID:36365633] [10.3390/polym14214636]
6. Dongxue Cao, Enwei Wei, Zeyu Wang, Zhengyu Hu, Ling Qi, Hongli Zhou, Jingli Zhao.  (2022)  Microwave-assisted extraction, structural elucidation, and in vitro anti-glioma and immunostimulatory activity of polysaccharide from Panax ginseng C. A. Meyer.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2022.115729]
7. Arabi Maryam, Ostovan Abbas, Wang Yunqing, Mei Rongchao, Fu Longwen, Li Jinhua, Wang Xiaoyan, Chen Lingxin.  (2022)  Chiral molecular imprinting-based SERS detection strategy for absolute enantiomeric discrimination.  Nature Communications,  13  (1): (1-14).  [PMID:36180485] [10.1038/s41467-022-33448-w]
8. Tingting Li, Haiqiong Ma, Hong Li, Hao Tang, Jinwen Huang, Shiying Wei, Qingxia Yuan, Xiaohuo Shi, Chenghai Gao, Shunli Mi, Longyan Zhao, Shengping Zhong, Yonghong Liu.  (2022)  Physicochemical Properties and Anticoagulant Activity of Purified Heteropolysaccharides from Laminaria japonica.  MOLECULES,  27  (9): (3027).  [PMID:35566376] [10.3390/molecules27093027]
9. Shuo Shi, Guocheng Wang, Jie Liu, Sunan Liu, Qiuyu Xu, Xi Lan, Jianxing Feng, Jing Sun, Wentao Zhang, Jianlong Wang.  (2021)  Gentiana straminea Maxim. polysaccharide decolored via high-throughput graphene-based column and its anti-inflammatory activity.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:34774595] [10.1016/j.ijbiomac.2021.11.010]
10. Manli Guo, Jingtian Chi, Chi Zhang, Minglin Wang, Hui Liang, Juying Hou, Shiyun Ai, Xiangyang Li.  (2020)  A simple and sensitive sensor for lactose based on cascade reactions in Au nanoclusters and enzymes co-encapsulated metal-organic frameworks.  FOOD CHEMISTRY,      [PMID:32871299] [10.1016/j.foodchem.2020.127863]
11. Baolei Fan, Guoliang Wei, Xiaofeng Gan, Tingting Li, Zengyi Qu, Sheng Xu, Chao Liu, Chunqi Qian.  (2020)  Study on the varied content of Polygonatum cyrtonema polysaccharides in the processing of steaming and shining for nine times based on HPLC-MS/MS and chemometrics.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2020.105352]
12. Guo Zongren, Long Liangkun, Ding Shaojun.  (2020)  Characterization of an L-Arabinose Isomerase from Bacillus velezensis and Its Application for L-Ribulose and L-Ribose Biosynthesis.  APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY,  192  (3): (935-951).  [PMID:32617845] [10.1007/s12010-020-03380-0]
13. Hui Wang, Meiyin Wang, Jining Shang, Yuanhang Ren, Bin Yue, Heyong He.  (2020)  H3PMo12O40 Immobilized on Amine Functionalized SBA-15 as a Catalyst for Aldose Epimerization.  Materials,  13  (3): (507).  [PMID:31973194] [10.3390/ma13030507]
14. Guo Zongren, Long Liangkun, Ding Shaojun.  (2019)  Characterization of a d-lyxose isomerase from Bacillus velezensis and its application for the production of d-mannose and l-ribose.  AMB Express,  (1): (1-11).  [PMID:31529161] [10.1186/s13568-019-0877-3]
15. Hong-Xun Wang, Yang Yi, Jie Sun, Olusola Lamikanra, Ting Min.  (2018)  Fingerprint profiling of polysaccharides from different parts of lotus root varieties.  RSC Advances,  (30): (16574-16584).  [PMID:35540557] [10.1039/C8RA01104D]
16. Yuanqi Duan, Zhengyu Hu, Long Jin, Tieqiang Zong, Xiaohui Zhang, Yanan Liu, Pengcheng Yang, Jinfeng Sun, Wei Zhou, Gao Li.  (2024)  Efficient degradation and enhanced anticomplementary activity of Belamcanda chinensis (L.) DC. polysaccharides via trifluoroacetic acid treatment with different degrees.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39084989] [10.1016/j.ijbiomac.2024.134117]
17. Xiaohui Zhang, Zhengyu Hu, Yuanqi Duan, Yuxin Jiang, Weiwei Xu, Pengcheng Yang, Wei Zhou, Jinfeng Sun, Gao Li.  (2024)  Extraction, characterization, and neuroprotective effects of polysaccharides the stems of Panax ginseng C. A. Meyer by three different solvents (water, acid, alkali).  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2024.119512]
18. Weiwei Xu, Wei Zhou, Jinfeng Sun, Weiwei Chen, Xuanye Wu, Tong Guan, Yilin Zhao, Pengcheng Yang, Zhengyu Hu, Gao Li.  (2024)  Isolation, structural characterization, and hypoglycemic activity of polysaccharides from the stems of Panax ginseng C. A. Meyer.  Frontiers in Sustainable Food Systems,      [PMID:] [10.3389/fsufs.2024.1500278]
19. Chang Shuaishuai, Lei Xuanhao, Xu Weijia, Guan Feng, Ge Jian, Nian Fuzhao.  (2024)  Preparation and characterization of Tobacco polysaccharides and its modulation on hyperlipidemia in high-fat-diet-induced mice.  Scientific Reports,  14  (1): (1-20).  [PMID:39500936] [10.1038/s41598-024-77514-3]
20. Yiming Wang, Wensheng Wei, Yuxin Wang, Guangwen Xu, Jinggang Zhao, Lei Shi.  (2024)  Promotion mechanism of hydroxyl groups in catalyzing CO2 cycloaddition.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2024.102999]
21. Yongchun Huang, Jie Bai, Jinman Shui, Zhanhai Su, Chengzhu Cao, Haiyan Wang, Qiong Wu, Shoude Zhang.  (2025)  Simultaneous determination of the monosaccharide types and their absolute configurations in polysaccharides based on UPLC-MS/MS.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39788268] [10.1016/j.ijbiomac.2025.139647]
22. Lihan Yue, Ming Zhao, Qiang Zhou, Liqiu Sun, Dan Wang, Jun Li, Zhichun Shi.  (2025)  Isolation, Purification, Structural Characterization, and the Antioxidant Activities of Polysaccharides Extracted from Isatidis Radix.  ChemistrySelect,  10  (25): (e00963).  [PMID:] [10.1002/slct.202500963]
23. Wei Zong, Zijing Liu, Haiyan Lan, Jianwei Yang, Yuxuan Xia, Zhongsheng Xu, Li Mai, Jie Wang, Yixi Bao.  (2025)  Structural characterization of a pectin polysaccharide from Phyllanthus emblica fruits and their antitumor effect via macrophage polarization in the cold immune microenvironment.  CARBOHYDRATE POLYMERS,      [PMID:40973298] [10.1016/j.carbpol.2025.124287]
24. Zuoying Wang, Sida Zhang, Yue Li, Zhuoshuo Zhou, Xu Zhang, Ying Chen, Yanli Zhao, Cai Ye, Jinlian Li, Naitian Zhang, Dongmei Wu.  (2025)  Structural characterization and effect of activating autophagy and regulating oxidative stress of polysaccharide from fibrous roots of Atractylodes chinensis.  BIOORGANIC CHEMISTRY,      [PMID:40412222] [10.1016/j.bioorg.2025.108609]
25. Yuanqi Duan, Jinfeng Sun, Yongkang Xue, Weiwei Xu, Yuxin Jiang, Tieqiang Zong, Wei Zhou, Zhengyu Hu, Gao Li.  (2025)  Physicochemical Properties and Cytoprotective Effects on PC12 Cells of Polysaccharides from Belamcanda chinensis (L.) DC. Obtained via a Gradient Ethanol Precipitation Method.  MOLECULES,  30  (5): (998).  [PMID:40076223] [10.3390/molecules30050998]
26. Jie Bai, Yongchun Huang, Yuling Zhao, Lirong Zhang, Fuli Zhu, Yixizhuoma, Yuxin Weng, Shoude Zhang.  (2026)  Determination of the monosaccharide types and absolute configurations in polysaccharides with (S)-(-)-1-phenylethylamine based on UPLC-MS/MS.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41638272] [10.1016/j.ijbiomac.2026.150674]
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