5-Hydroxymethyl-2-furancarboxylic acid - 10mM in DMSO , CAS No.6338-41-6

CAS: 6338-41-6 Cat. No.: H425212 Molecular Weight: 142.1 EC Number: 675-513-1
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GRADE & PURITY 10mM in DMSO
Synonyms
CHEBI:89118 | ethyl 2-aminopropanoate;hydrochloride | 5-(Hydroxymethyl)-2-furoic acid | AS-18462 | Nepsilon-Cbz-D-lysine | DTXSID5033098 | AM20100567 | Tox21_201082 | 1,2-dioctadecanoyl-rac-glycerol | 5-hydroxymethylfurancarboxylic acid | AKOS000505137 |
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
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Size
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Price
Qty
1ml
H425212-1ml
1
$23.90
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 114 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
CHEBI:89118 | ethyl 2-aminopropanoate;hydrochloride | 5-(Hydroxymethyl)-2-furoic acid | AS-18462 | Nepsilon-Cbz-D-lysine | DTXSID5033098 | AM20100567 | Tox21_201082 | 1, 2-dioctadecanoyl-rac-glycerol | 5-hydroxymethylfurancarboxylic acid | AKOS000505137 |
Specifications & Purity
10mM in DMSO
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers
Canonical SmilesC1=C(OC(=C1)C(=O)O)CO
IUPAC Name5-(hydroxymethyl)furan-2-carboxylic acid
InChIKeyPCSKKIUURRTAEM-UHFFFAOYSA-N
INCHI1S/C6H6O4/c7-3-4-1-2-5(10-4)6(8)9/h1-2,7H,3H2,(H,8,9)
Isomeric SMILES C1=C(OC(=C1)C(=O)O)CO
Molecular Weight 142.1
Reaxy-Rn 121784
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=121784&ln=

Documentation

📋 Safety Data Sheet (SDS)

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

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✅ Certificate of Analysis (COA)

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

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📊 Datasheet

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🔬 Specification Sheet

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClassFurans
SubclassFuroic acid and derivatives
Intermediate Tree Nodes Not available
Direct ParentFuroic acids
Alternative Parents Heteroaromatic compounds  Oxacyclic compounds  Monocarboxylic acids and derivatives  Carboxylic acids  Primary alcohols  Organic oxides  Hydrocarbon derivatives  Aromatic alcohols  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Furoic acid - Heteroaromatic compound - Oxacycle - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as furoic acids. These are organic compounds containing a furoic acid moiety, with a structure characterized by a furan ring bearing a carboxylic acid group at the C2 or C3 carbon atom.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
LCK Tclin Tyrosine-protein kinase LCK (9212 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
pol Human immunodeficiency virus type 1 reverse transcriptase (18245 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Priestia megaterium (1154 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Microbotryum violaceum (192 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Aspergillus pseudoglaucus (84 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mycotypha microspora (91 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
[Chlorella] fusca (158 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

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1 results found

Lot NumberCertificate TypeDateItem
I2226187Certificate of AnalysisMay 07, 2026 H425212
Chemical and Physical Properties
Sensitivityheat & air sensitive
Melt Point(°C)161 °C
Molecular Weight142.110 g/mol
XLogP30.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count2
Exact Mass142.027 Da
Monoisotopic Mass142.027 Da
Topological Polar Surface Area70.700 Ų
Heavy Atom Count10
Formal Charge0
Complexity134.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
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
References
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51. Xinkang Peng, Xulong Song, Wei Cao, Zhenchen Tang, Tingting Wang, Yunxia Wen, Zhinan Wu, Tong Zhou, Han Lin, Xiaohua Lu, Tuo Ji, Jiahua Zhu.  (2025)  Microwave-Activated Peroxyl Radicals Accelerate Hydroxymethyl Oxidation on the AuPd/C Catalyst for Mild Synthesis of FDCA.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.4c07309]
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53. Hao Chen, Si-Ru Chen, Qing Yang, Le-Xing You, Qun-Feng Ye, Ai-Jun Wang, Dong-Hai Lin, Yan-Xia Jiang, Shi-Gang Sun.  (2024)  Nickel sulfide nanorods encapsulated in Nitrogen-Doped carbon on nickel foam in situ derived from Saccharomycetes cerevisiae for the selective oxidation of biomass.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.155922]
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68. Ren Yue, Kong Wei, Li Yang, Zhan Wang, Zhang Chunyu, Miao Yuhang, Yao Bingxin, Li Shengnan, Li Zhenhua, Liu Xiang, Zhan Sheng, Zhou Hua, Shao Mingfei, Duan Haohong.  (2025)  Selective electrooxidation of 5-hydroxymethylfurfural at pilot scale by engineering a solid polymer electrolyte reactor.  Nature Catalysis,      [PMID:] [10.1038/s41929-025-01374-x]
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72. Huan Wen, Xizi Wu, Zelong Sun, Zhangyue Zheng, Junxin Chen, Jia Wu, Shibin Yin.  (2025)  Interface-engineered Co5.47N-W5N4 heterostructure catalyst with synergistic dual-site hydrogen bonding and electronic modulation for efficient 5-hydroxymethylfurfural electrooxidation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40929822] [10.1016/j.jcis.2025.138915]
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77. Xiangdong Ma, Shan Yue, Rui Liu, Hui Kan, Jiayi Gao, Mingjing Zhao, Haijiao Xie, Xiaohong Xia.  (2025)  Micro-nickel doping regulates the surface electron and structure of materials for optimizing biomass upgrading.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2025.183699]
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79. Zhichen Liu, Tiantian Xiao, Xinru Wu, Cejun Hu, Xue Feng Lu, Hongwei Zhang, Jiujun Zhang, Xiaojun Bao, Pei Yuan.  (2025)  Cu-induced Ni3 + -O active sites in Prussian blue analogues enable nearly 100 % selective electrooxidation of 5-hydroxymethylfurfural to produce kilogram-scale 2,5-furandicarboxylic acid.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2025.125601]
80. Abdul Qayum, Karim Harrath, Xueqi Wang, Pengfei Xie, Yanran Cui, Yuanyuan Li, Junyan Zhang, Zili Wu, Xiangbei Wan, Amani Ebrahim, Sainan Yuan, Zhenglong Li.  (2025)  Galvanic replacement assisted in situ solution combustion synthesis of copper-cobalt oxide heterointerface catalyst for electrocatalytic oxidation of 5-hydroxymethylfurfural.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.162654]
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82. Yanan Wei, Tao Xia, Tongyu Zhong, Henghui Zhu, Yucai He, Yunlei Zhang.  (2025)  Frustrated Lewis pairs engineering on CeO2 to boost BHMF oxidation activity of AuPd for efficient production of FDCA.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2025.163538]
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86. Shuo Zhang, Xue Yang, Longyongxue Ma, Junwei Ma, Hongtao Gao.  (2025)  Efficient electrocatalytic oxidation of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid using an amorphous bimetallic Ni–Co hydroxide with filamentous structure in alkaline media.  Materials Today Chemistry,      [PMID:] [10.1016/j.mtchem.2025.103095]
87. Maolin Li, Quanxi Lu, Zhichao Dong, Sijie Liu, Rong Tan.  (2025)  Efficient strategy for fructose conversion to 2,5-furandicarboxylic acid, 2,5-dicarbonylfuran or 5-formyl-2-furancarboxylic acid over dual single-atomic Fe/Co catalyst.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.169405]
88. Hongchen Liu, Jinxiu Qian, Fan Yang, JunPu An, Chunhui Yu, Junwei Yuan, Jiahui Liu, Meitong Zhao, Aocheng Wang, Yongfeng Li.  (2025)  Interfacial assembled CoP and CeO2 heterostructure nanosheets array for efficient 5-hydroxymethylfurfural electrooxidation coupled with hydrogen evolution.  RENEWABLE ENERGY,      [PMID:] [10.1016/j.renene.2025.124644]
89. Gang Jin, Tao Zhao, Yunzhen Jia, Dazhong Zhong, Jinping Li, Qiang Zhao.  (2025)  Oxygen vacancy enabling CoO2 formation: A key boost for efficient electrocatalytic 5-hydroxymethylfurfural oxidation over CoOx.  Journal of Energy Chemistry,      [PMID:] [10.1016/j.jechem.2025.10.049]
90. Xingchun Shi, Qian Zhang, Jinting Wu, Haijiao Lu, Hao Qin, Xiao-Dong Zhu, Jian Gao, Yong-Chao Zhang.  (2025)  Unlocking the role of oxygen vacancies in FeO/NiO/Ni for boosting 5-hydroxymethylfurfural electrooxidation.  AICHE JOURNAL,      [PMID:] [10.1002/aic.70150]
91. Yan Li, Fan Yang, Xuemei Tan, Yitong Li, Chunjie Gong, Huanan Li, Wanli Cheng, Wenjing Xiao, Jiashu Liu, Zhengbing Jiang.  (2025)  Lipase and alcohol oxidase cascade catalytic system for the efficient conversion of 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41260435] [10.1016/j.ijbiomac.2025.149081]
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99. Junxiang Wang, Xu Wang, Xiaoyan Liu, Yanfei Feng, Yukun Wan, Hui Yang.  (2025)  Strategies to increase the selective electrocatalytic oxidation of 5-hydroxymethylfurfural to produce 2,5-furanedicarboxylic acid.  BIOMASS & BIOENERGY,      [PMID:] [10.1016/j.biombioe.2025.108835]
100. Chengfeng Yi, Jingwen Li, Jiarui Li, Bingchuan Xue, Xing Lin, Zhigang Liu.  (2025)  Tunable Ni(OH)2/N,W-Ni3S2 heterostructures to balance the competitive adsorption of 5-hydroxymethylfurfural and OH− for biomass valorization.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.171492]
101. Cheng-Feng Yi, Jing-Wen Li, Jia-Rui Li, Bing-Chuan Xue, Xing Lin, Zhi-Gang Liu.  (2025)  N,W-Cooperative Modulation of Ni3S2 for Efficient Electrocatalytic Oxidation of 5-Hydroxymethylfurfural to 2,5-Furandicarboxylic Acid.  RARE METALS,      [PMID:] [10.1002/rar2.70061]
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104. Hao-Yue Ma, Jun-Fei Gu, Xing-Chuan Li, Zhan Chen, Qi-Yu Fu, Francis Verpoort, Wen-Jie Mo, Zheng Liu, Cheng Chen, Soon Hyeok Hong, Zongkui Kou.  (2026)  Facile molten salt synthesis of Co@N-C catalysts enables highly efficient HMF-to-FDCA conversion under mild conditions.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.172617]
105. Wenting Cai, Shuai Liu, Tongxue Zhang, Ke Fan, Xubin Zhang, Fumin Wang, Jing-Jing Lv, Xijun Liu.  (2026)  Heterojunction engineering of Co3S4 to modulate NiO for efficient electrooxidation of 5-hydroxymethylfurfural.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2026.173178]
106. Yuwei Xiong, Chen Deng, Wei Ji, Yifei Sun, Richen Lin.  (2026)  Phosphorus-assisted reconstruction creates NiOOH/CoOOH interfaces for efficient biomass-derived 5-hydroxymethylfurfural electrooxidation.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2026.126489]
107. Biao Meng, Qing Xu, Xiaoling Liu, Qizhi Hu, Menglin Xie, Xiao Xu, Yu Zhou, Zhen Meng, Jun Wang.  (2026)  Synergistic Alloy and Support Effects in Covalent Organic Framework-Stabilized AuPd Catalysts for Aerobic 5-Hydroxymethylfurfural Oxidation to 2,5-Furandicarboxylic Acid.  CHEMISTRY-A EUROPEAN JOURNAL,      [PMID:41532793] [10.1002/chem.202503324]
108. Ziyao Li, Nan Wang, Bo Li, Xuzhuo Sun, Jing Chen.  (2026)  Cobalt Nanoparticles Encapsulated in Nitrogen-Doped Carbon Nanotubes for Highly Efficient Electrochemical Oxidation of 5-Hydroxymethylfurfural Coupled with 4-Nitrophenol Hydrogenation.  ACS Sustainable Chemistry & Engineering,      [PMID:] [10.1021/acssuschemeng.5c08925]
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110. Yifei Ye, Zhuoshen Huang, Hao Pan, Zhaokun Wang, Wei Xia, Guangtong Hai, Ge Wang, Xiubing Huang.  (2026)  Enhancing electrocatalytic oxidation of 5-hydroxymethylfurfural via Ce(4f)–O(2p)–TM(3d) orbital coupling to modulate reactant adsorption equilibrium.  Journal of Energy Chemistry,      [PMID:] [10.1016/j.jechem.2026.02.028]
111. Yanan Chang, Qiao Tan, Qingjun Jiang, Xuexuan Zhong, Xiaoxuan Li, Jianchun Bao, Jie Zhang, Dongdong Xu, Ying Liu.  (2026)  Synergistic Mott-Schottky and plasmonic effects promote reactive oxygen species production and reactant adsorption for efficient 5-hydroxymethylfurfural upgrading.  Journal of Energy Chemistry,      [PMID:] [10.1016/j.jechem.2026.03.021]
112. Lin Zhou, Zhanghong Guo, Haining Cui, Jinxin Ma, Chan Wang, Qijun Song.  (2026)  Magnetic γ-Fe2O3@Ir Nanozyme for Molar-Level 5-Hydroxymethylfurfural Oxidation With Atmosphere Oxygen.  CHEMISTRY-A EUROPEAN JOURNAL,      [PMID:] [10.1002/chem.202503637]
113. Peiyun Zhou, Shihao Feng, Xi Wang, Xiang Liu, Xingjian Xu, Xiubing Huang, Haohong Duan.  (2026)  Breaking the Kinetic Limitation of Acidic 5-Hydroxymethylfurfural Electrooxidation to 2,5-Furandicarboxylic Acid via Shared Oxygen Intermediates with Oxygen Evolution Reaction on Ir-MnOx.  ACS Catalysis,      [PMID:] [10.1021/acscatal.6c00426]
114. Haojie Feng, Ju Huang, Yuanyuan Wang, Shichao Du, Xiaolei Wang, Ying Xie, Yu Fu, Mingxia Li, Zhimin Chen, Zhiyu Ren.  (2026)  Expanding the operational horizon of ampere-scale biomass electrorefining via decoupling competing pathways on cuprous-integrated spinel heterostructures.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2026.126945]
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