D-Histidine - Moligand™, ≥99% , CAS No.351-50-8

CAS: 351-50-8 Cat. No.: H105705 Molecular Weight: 155.15 Beilstein Registry Number: 84089 EC Number: 206-513-8
AVAILABLE TO ORDER
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%
Synonyms
HISTIDINE, D- | NCGC00142611-01 | Reumacide | HY-W012572 | H0998 | STL141076 | Histidine, monohydrochloride, D- | (R)-2-Amino-3-(4-imidazolyl)propionic acid | D-Histidine, >=98% (TLC) | D-Histidine (H-D-His-OH) | C06419 | DTXSID70889344 | NCGC00142611-02
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
H105705-1g
4
$9.90
5g
H105705-5g
5
$10.90
25g
H105705-25g
3
$36.90
100g
H105705-100g
4
$129.90
500g
H105705-500g
1
$519.90
Enter a quantity for the sizes you want to add.
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Why this grade

Moligand™, ≥99% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal 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 36 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
HISTIDINE, D- | NCGC00142611-01 | Reumacide | HY-W012572 | H0998 | STL141076 | Histidine, monohydrochloride, D- | (R)-2-Amino-3-(4-imidazolyl)propionic acid | D-Histidine, >=98% (TLC) | D-Histidine (H-D-His-OH) | C06419 | DTXSID70889344 | NCGC00142611-02
Specifications & Purity
Moligand™, ≥99%
Biochemical and Physiological Mechanisms
D-Histidine may be used in the design of peptide drugs, cationic peptides, such as analogues of carnosine. D-Histidine may also be used as a heavy metal sequestration agent.
Storage
Room temperature
Shipped In
Normal
Grade
Moligand™
Action Type
INHIBITOR
Purity
≥99%
Names and Identifiers
Pubchem Sid488184643
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184643
Canonical SmilesC1=C(NC=N1)CC(C(=O)O)N
IUPAC Name(2R)-2-amino-3-(1H-imidazol-5-yl)propanoic acid
InChIKeyHNDVDQJCIGZPNO-RXMQYKEDSA-N
INCHI1S/C6H9N3O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1,7H2,(H,8,9)(H,10,11)/t5-/m1/s1
Isomeric SMILES C1=C(NC=N1)C[C@H](C(=O)O)N
WGK Germany 1
Molecular Weight 155.15
Beilstein 84089
Reaxy-Rn 7800
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7800&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 acids and derivatives
ClassCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentHistidine and derivatives
Alternative Parents D-alpha-amino acids  Imidazolyl carboxylic acids and derivatives  Aralkylamines  Heteroaromatic compounds  Amino acids  Monocarboxylic acids and derivatives  Carboxylic acids  Azacyclic compounds  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Histidine or derivatives - Alpha-amino acid - D-alpha-amino acid - Imidazolyl carboxylic acid derivative - Aralkylamine - Azole - Imidazole - Heteroaromatic compound - Amino acid - Carboxylic acid - Azacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Primary amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Amine - Aromatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as histidine and derivatives. These are compounds containing cysteine or a derivative thereof resulting from reaction of cysteine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Other amino acids
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA3 Tclin Carbonic anhydrase III (753 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5B Tclin Carbonic anhydrase VB (957 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA5A Tclin Carbonic anhydrase VA (1168 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC7A5 Tchem L-type amino acid transporter 1 (388 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ca7 Carbonic anhydrase VII (3 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca13 Carbonic anhydrase XIII (322 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase (69 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ca15 Carbonic anhydrase 15 (173 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CAN2 Carbonic anhydrase 2 (140 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Carbonic anhydrase-like protein, putative (25 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:

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

26 results found

Lot NumberCertificate TypeDateItem
D2624242Certificate of AnalysisApr 10, 2026 H105705
D2624241Certificate of AnalysisApr 10, 2026 H105705
D2624240Certificate of AnalysisApr 10, 2026 H105705
D2624239Certificate of AnalysisApr 10, 2026 H105705
L2106555Certificate of AnalysisSep 09, 2025 H105705
C1810049Certificate of AnalysisMar 04, 2025 H105705
D2422024Certificate of AnalysisMar 20, 2024 H105705
D2422025Certificate of AnalysisMar 20, 2024 H105705
D2528027Certificate of AnalysisNov 10, 2022 H105705
L2518062Certificate of AnalysisNov 10, 2022 H105705
I2424079Certificate of AnalysisNov 10, 2022 H105705
I2424078Certificate of AnalysisNov 10, 2022 H105705
A2310340Certificate of AnalysisNov 10, 2022 H105705
C2626140Certificate of AnalysisNov 10, 2022 H105705
C2418078Certificate of AnalysisNov 10, 2022 H105705
A2310361Certificate of AnalysisNov 10, 2022 H105705
A2310358Certificate of AnalysisNov 10, 2022 H105705
A2310353Certificate of AnalysisNov 10, 2022 H105705
A2310345Certificate of AnalysisNov 10, 2022 H105705
A2310344Certificate of AnalysisNov 10, 2022 H105705
A2310343Certificate of AnalysisNov 10, 2022 H105705
C1810048Certificate of AnalysisJan 27, 2022 H105705
I2308187Certificate of AnalysisNov 18, 2021 H105705
I2426393Certificate of AnalysisNov 18, 2021 H105705
J2227142Certificate of AnalysisNov 18, 2021 H105705
K2510117Certificate of AnalysisNov 18, 2021 H105705

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Chemical and Physical Properties
SolubilitySoluble in water and 1 M HCl (50 mg/ml).
Specific Rotation[α]-13 ° (C=11, 6mol/L HCl)
Melt Point(°C)287°C
Molecular Weight155.150 g/mol
XLogP3-3.200
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count4
Rotatable Bond Count3
Exact Mass155.069 Da
Monoisotopic Mass155.069 Da
Topological Polar Surface Area92.000 Ų
Heavy Atom Count11
Formal Charge0
Complexity151.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
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
1. Jianrong Wang, Sha Han, Hongfang Zhao, Hongxia Li, Xiaohui Niu, Yi Wang, Kunjie Wang.  (2023)  Electrochemical enantioselective recognition by defined chiral linkers in polysaccharides modified with carbon quantum dots.  ELECTROANALYSIS,      [PMID:] [10.1002/elan.202300301]
2. Xiang Huang, Chenxin Lu, Wenjie Zhang, Lulu Liu, Zhengbao Zha, Zhaohua Miao.  (2023)  Chiral Sulfur Nanosheets for Dual-Selective Inhibition of Gram-Positive Bacteria.  ACS Nano,      [PMID:37466081] [10.1021/acsnano.3c03458]
3. Feiyan Wang, Linhong Liao, Xiaohui Liu, Jie Zhang, Fengshou Wu.  (2023)  Porphyrin-based porous organic frameworks as efficient peroxidase mimics for selective detection of hydrogen peroxide and glucose.  INORGANIC CHEMISTRY COMMUNICATIONS,      [PMID:] [10.1016/j.inoche.2023.111011]
4. Niu Xiaohui, Zhao Rui, Yan Simeng, Li Hongxia, Yang Jing, Cao Kunjie, Liu Xiaoyu, Wang Kunjie.  (2023)  Chiral MOFs encapsulated by polymers with poly-metallic coordination as chiral biosensors.  MICROCHIMICA ACTA,  190  (6): (1-12).  [PMID:37208529] [10.1007/s00604-023-05807-x]
5. Xiaohui Niu, Simeng Yan, Rui Zhao, Hongxia Li, Xiaoyu Liu, Kunjie Wang.  (2023)  Design and Electrochemical Chiral Sensing of the Robust Sandwich Chiral Composite d-His-ZIF-8@Au@ZIF-8.  ACS Applied Materials & Interfaces,      [PMID:37126450] [10.1021/acsami.3c03947]
6. Li Gao, Piao Xu, Jiaoyan Ren.  (2023)  A sensitive and economical method for simultaneous determination of D/L- amino acids profile in foods by HPLC-UV: Application in fermented and unfermented foods discrimination.  FOOD CHEMISTRY,      [PMID:36628920] [10.1016/j.foodchem.2022.135382]
7. Du Jinyan, Xu Na, Wang Chaofeng, Shu Qin, Xu Qidi, Zhang Ping, Zhuo Shujuan, Zhu Changqing.  (2022)  Red emission B, N, S-co-doped carbon dots with pH-responsive functionality for colorimetric and fluorescent dual-mode detection of Ag+ ions.  JOURNAL OF MATERIALS SCIENCE,  57  (47): (21693-21708).  [PMID:] [10.1007/s10853-022-07988-x]
8. 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]
9. Shuyu Xiao, Jiechun Liang, Junzi Li, Jiaji Cheng, Xi Zhu, Tingchao He.  (2022)  Tunable optical activities in chiral transition metal oxide nanoparticles.  Nanoscale,  14  (41): (15414-15421).  [PMID:36218542] [10.1039/D2NR02555H]
10. Feiyan Liu, Xuandi Lai, Shengliang Zhao, Zhiyang Lu, Peigang Han, Liqiong Chen.  (2022)  A simple and feasible fluorescent approach for rapid detection of hexavalent chromium based on gold nanoclusters.  FOOD CHEMISTRY,      [PMID:36137372] [10.1016/j.foodchem.2022.134251]
11. Hongxia Li, Letong Wang, Simeng Yan, Jinliang Chen, Mengmeng Zhang, Rui Zhao, Xiaohui Niu, Kunjie Wang.  (2022)  Fusiform-like metal-organic framework for enantioselective discrimination of tryptophan enantiomers.  ELECTROCHIMICA ACTA,      [PMID:] [10.1016/j.electacta.2022.140409]
12. Shutong Yang, Liancheng Gu, Fangling Wu, Xinhua Dai, Fuxing Xu, Qiaoyu Li, Xiang Fang, Shaoning Yu, Chuan-Fan Ding.  (2022)  The chirality determination of amino acids by forming complexes with cyclodextrins and metal ions using ion mobility spectrometry, and a DFT calculation.  TALANTA,      [PMID:35272154] [10.1016/j.talanta.2022.123363]
13. Liu Chun, Pang Qiwei, Wu Tong, Qi Wenjing, Fu Wensheng, Wang Yi.  (2021)  A Rapid Visual Detection of Ascorbic Acid Through Morphology Transformation of Silver Triangular Nanoplates.  Journal of Analysis and Testing,  (3): (210-216).  [PMID:] [10.1007/s41664-021-00174-z]
14. Lamei Yang, Feng Luo, Weili Wei.  (2021)  Simultaneous determination of the concentration and enantiomeric excess of amino acids with a coumarin-derived achiral probe.  Analytical Methods,  13  (16): (1905-1910).  [PMID:33913945] [10.1039/D1AY00271F]
15. Zehao Gu, Mengfan Lu, Kai Feng, Zhaoxia Jin.  (2021)  The different composites of cellulose nanocrystals with D- or L-histidine.  Nanoscale,  13  (17): (8174-8180).  [PMID:33881430] [10.1039/D1NR00946J]
16. Zou Jiao, Lan Xi-Wen, Zhao Guo-Qing, Huang Zhao-Ning, Liu Yi-Ping, Yu Jin-Gang.  (2020)  Immobilization of 6-O-α-maltosyl-β-cyclodextrin on the surface of black phosphorus nanosheets for selective chiral recognition of tyrosine enantiomers.  MICROCHIMICA ACTA,  187  (11): (1-11).  [PMID:33141322] [10.1007/s00604-020-04606-y]
17. Jiao Zou, Jin-Gang Yu.  (2020)  Nafion-stabilized black phosphorus nanosheets-maltosyl-β-cyclodextrin as a chiral sensor for tryptophan enantiomers.  Materials Science & Engineering C-Materials for Biological Applications,      [PMID:32409064] [10.1016/j.msec.2020.110910]
18. Jiao Zou, Jin-Gang Yu.  (2019)  Chiral recognition of tyrosine enantiomers on a novel bis-aminosaccharides composite modified glassy carbon electrode.  ANALYTICA CHIMICA ACTA,      [PMID:31623714] [10.1016/j.aca.2019.08.018]
19. Lijun Zhang, Zhen Liu, Can Xiong, Lei Zheng, Yunsheng Ding, Hongbo Lu, Guobing Zhang, Longzhen Qiu.  (2018)  Selective recognition of Histidine enantiomers using novel molecularly imprinted organic transistor sensor.  ORGANIC ELECTRONICS,      [PMID:] [10.1016/j.orgel.2018.05.063]
20. Tao Liu, Yingying Su, Hongjie Song, Yi Lv.  (2013)  Microwave-assisted green synthesis of ultrasmall fluorescent water-soluble silver nanoclusters and its application in chiral recognition of amino acids.  ANALYST,  138  (21): (6558-6564).  [PMID:24029964] [10.1039/C3AN01343J]
21. Wenrong Cai, Yanjing Shi, Ning Liu, Zheng-Zhi Yin, Junyao Li, Laidi Xu, Datong Wu, Yong Kong.  (2024)  A photothermal effect-based chiral sensor for chiral discrimination and sensitive detection.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:38788508] [10.1016/j.saa.2024.124494]
22. Wenjing Wang, Guangrong Lu, Zhichao Deng, Huanyu Li, Wenfang He, Shouxing Yang, Yuanyuan Zhu, Chenxi Xu, Yujie Zhang, Lanqi Wang, Xiaoling Huang, Mingzhen Zhang, Changlong Xu.  (2024)  Biocompatible carbon dots nanozymes as ROS/RNS modulators for ulcerative colitis alleviation by comprehensively orchestrating intestinal homeostasis.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2024.157800]
23. Ruxuan Ma, Liuting Zheng, Han Yu, Da Huo, Huiyue Zhao, Hao Zhang.  (2025)  Chirality engineering-regulated liquid–liquid phase separation of stress granules and its role in chemo-sensitization and side effect mitigation.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:39862843] [10.1016/j.jcis.2025.01.177]
24. Yi-Ting Gu, Dong-Jin Qian.  (2024)  Construction of multi(iron)porphyrin array multilayers on quartz surface as peroxidase mimetics for H2O2 and glucose colorimetric, fluorometric and color-read detection.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2024.110735]
25. Wuming Wu, Xiaolian Jiang, Qin Zeng, Huiyu Zou, Chunyan Deng.  (2024)  Facile and green synthesis of Au nanoparticles decorated Epigallocatechin-3-Gallate nanospheres with enhanced performance in stability, photothermal conversion and nanozymatic activity.  Biomaterials Advances,      [PMID:39317045] [10.1016/j.bioadv.2024.214050]
26. Yifei Ma, Lijie Zhang, Hong Yang, Shanshan Zhu, Jinhua Liu.  (2025)  Imidazole-triggered in situ fluorescence reaction system for quantitatively determination of dopamine from multiple sources.  TALANTA,      [PMID:40157196] [10.1016/j.talanta.2025.127975]
27. Yuanyi Wu, Yumei Xiao, Yang Ju, Yanque Sun, Jialin He, Tian Liu, Miao He, Kaiyong Wang, Yi Yang.  (2024)  Multi-mode sensing platform for gallic acid determination based on the peroxidase-like activity of magnetic Fe3O4@Co/Ni/Al-LDH nanospheres.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2024.116366]
28. Luzheng Dong, Jun Wu, Xiashi Zhu.  (2024)  Preparation of amino acid chiral ionic liquid and visual chiral recognition of glutamine and phenylalanine enantiomers.  CHIRALITY,  36  (4): (e23665).  [PMID:38570326] [10.1002/chir.23665]
29. Chan Wang, Yingyi Quan, Jiang Jiang, Han Yu, Jia Liu, Wei Tang, Xinyue Li, Shouju Wang, Da Huo, Guang-Liang Jiang, Yang Yang, Qingqing Ding.  (2025)  Protein Coronation-Induced Cancer Staging-Dependent Multilevel Cytotoxicity: An All-Humanized Study in Blood Vessel Organoids.  ACS Nano,      [PMID:39743836] [10.1021/acsnano.4c07783]
30. Yaxin Wang, Yajie Zhou, Shanshan Zhao, Mingjiang Zhang, Anqi Li, Guangen Li, Qi Guo, Xueru Guo, Zhi Tong, Zeyi Li, Jing Lin, Taotao Zhuang.  (2024)  Recognizing chiral amino acids with a dual-optical-response system.  Journal of Materials Chemistry A,  12  (16): (9421-9426).  [PMID:] [10.1039/D3TA07645H]
31. Aumber Abbas, Qian Zhang, Jamal Kazmi, Ying Li, Wenbo Li, Waqas Ahmad, Chao Zou, Qijie Liang.  (2025)  Label-Free SERS Fingerprinting for Chiral Discrimination Using Chiral Two-Dimensional Superlattice.  NANO LETTERS,      [PMID:40763186] [10.1021/acs.nanolett.5c03047]
32. Jing Zhang, Ye Yang, Yi-Ping Liu, Guo-Cong Liu, Xi Zhu, Xin-Yu Jiang, Jin-Gang Yu.  (2025)  Highly selective and efficient recognition of tyrosine enantiomers at Au NPs/D-sorbitol/GCE-based chiral sensor.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2025.115424]
33. Zifang Zhang, Junhua Bai, Yan Gong, Lifang Zhang.  (2024)  Visual Detection of Ascorbic Acid via Smartphone with Portable Probe Based on Assembled FePO4@GO Peroxidase-like Nanozyme.  MOLECULES,  29  (21): (5097).  [PMID:39519738] [10.3390/molecules29215097]
34. Jing Zhang, Shuang-Ning Li, Yi-Ping Liu, Xin-Yu Jiang, Yue-Qin Liu, Jiao Zou, Jin-Gang Yu.  (2025)  An efficient and facile adonitol-based electrochemical chiral sensor for highly selective determination of tyrosine.  Journal of the Taiwan Institute of Chemical Engineers,      [PMID:] [10.1016/j.jtice.2025.106111]
35. Huimin Wang, Guangxin Wang, Ruoxi Liu, Jin Yong Lee, Shufeng Liu, Yingqi Tang, Jing Yu.  (2025)  Electrochemiluminescent Enantiodiscrimination on Chiral Engineered l-His-ZIF8.  LANGMUIR,      [PMID:41217085] [10.1021/acs.langmuir.5c03908]
36. Simin Zhang, Xiangfeng Chen, Yaping Shi, Xiangyu Zhu, Zongwei Cai.  (2026)  Soft-Chain-Induced Ultrahigh-Resolution Chiral Separation of Amino Acids via Bimetallic Immobilization in MALDI-TIMS-MS.  ANALYTICAL CHEMISTRY,      [PMID:41701523] [10.1021/acs.analchem.5c07869]
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