Copper D-gluconate - Moligand™,≥98% , CAS No.527-09-3

CAS: 527-09-3 Cat. No.: D133471 Peso molecular: 453.84 Beilstein Registry Number: 3(4)1256 Número EC: 208-408-2
Disponible para pedir
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. ≥98%
Synonyms
Copper(II) (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate | Copper(II) Gluconate
Storage
Room temperature,Argon charged
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
D133471-5g
2
9,90US$
25g
D133471-25g
4
10,90US$
100g
D133471-100g
5

14,90US$

22,90US$
Guardar 8,00 US$ (34.93%)
500g
D133471-500g
1
99,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

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

🌡

Storage & shipping

Room temperature,Argon charged Ships Normal 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Copper(II) Gluconate is a non-toxic copper supplement aid. Copper(II) Gluconate is the copper salt of D-gluconic acid. Copper(II) Gluconate as a precursor catalyst that can be used in the photo-induced polymerisation of acrylates.

Specifications

Sinónimos
Copper(II) (2R, 3S, 4R, 5R)-2, 3, 4, 5, 6-pentahydroxyhexanoate | Copper(II) Gluconate
Especificaciones y pureza
Moligand™, ≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature, Argon charged
Enviado en
Normal
Grado
Moligand™
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504751987
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504751987
Sonrisas canónicasC(C(C(C(C(C(=O)[O-])O)O)O)O)O.C(C(C(C(C(C(=O)[O-])O)O)O)O)O.[Cu+2]
IUPAC Namecopper;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate
InChIKeyOCUCCJIRFHNWBP-IYEMJOQQSA-L
INCHI1S/2C6H12O7.Cu/c2*7-1-2(8)3(9)4(10)5(11)6(12)13;/h2*2-5,7-11H,1H2,(H,12,13);/q;;+2/p-2/t2*2-,3-,4+,5-;/m11./s1
Isómeros SMILES C([C@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)O)O.C([C@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)O)O.[Cu+2]
WGK Alemania 3
RTECS LZ5058000
CAS alternativo 13005-35-1
Peso molecular 453.84
Beilstein 3(4)1256
Reaxy-Rn 11324943
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11324943&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 Not available
Direct ParentSugar acids and derivatives
Alternative Parents Medium-chain hydroxy acids and derivatives  Medium-chain fatty acids  Beta hydroxy acids and derivatives  Hydroxy fatty acids  Monosaccharides  Secondary alcohols  Carboxylic acid salts  Polyols  Carboxylic acids  Monocarboxylic acids and derivatives  Organic copper salts  Hydrocarbon derivatives  Organic oxides  Organic zwitterions  Carbonyl compounds  Primary alcohols  
Molecular FrameworkNot available
Substituents Gluconic_acid - Medium-chain hydroxy acid - Medium-chain fatty acid - Beta-hydroxy acid - Hydroxy fatty acid - Hydroxy acid - Fatty acyl - Fatty acid - Monosaccharide - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Organic transition metal salt - Monocarboxylic acid or derivatives - Polyol - Organic oxide - Organic copper salt - Hydrocarbon derivative - Organic salt - Carbonyl group - Organic zwitterion - Alcohol - Primary alcohol - Aliphatic acyclic compound
DescripciónThis compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
External Descriptors organic molecular entity
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.

21 results found

Lot NumberCertificate TypeFechaArticulo
E2625332Certificate of AnalysisMar 03, 2026 D133471
E2625333Certificate of AnalysisMar 03, 2026 D133471
E2625373Certificate of AnalysisMar 03, 2026 D133471
H2209334Certificate of AnalysisFeb 04, 2026 D133471
D2416067Certificate of AnalysisFeb 04, 2026 D133471
H2209333Certificate of AnalysisFeb 04, 2026 D133471
J2527026Certificate of AnalysisOct 30, 2025 D133471
A2206025Certificate of AnalysisJul 15, 2025 D133471
F2320148Certificate of AnalysisApr 09, 2025 D133471
F2320125Certificate of AnalysisApr 09, 2025 D133471
A2503305Certificate of AnalysisJan 09, 2025 D133471
K2412238Certificate of AnalysisNov 15, 2024 D133471
C2507114Certificate of AnalysisNov 15, 2024 D133471
G2408013Certificate of AnalysisMay 08, 2024 D133471
H2209330Certificate of AnalysisMay 08, 2024 D133471
H2209331Certificate of AnalysisMay 08, 2024 D133471
A2206024Certificate of AnalysisOct 13, 2023 D133471
A2206023Certificate of AnalysisOct 13, 2023 D133471
K21111042Certificate of AnalysisAug 17, 2023 D133471
K21111092Certificate of AnalysisAug 17, 2023 D133471
G2214011Certificate of AnalysisJul 19, 2022 D133471

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Propiedades químicas y físicas
SolubilidadSoluble in water. Insoluble in acetone, alcohol and ether
SensibilidadHygroscopic
Rotación específica [α]16.5° (C=1,H2O)
Punto de fusión (°C)155-157°
Peso molecular453.840 g/mol
XLogP3
Hydrogen Bond Donor Count10
Hydrogen Bond Acceptor Count14
Rotatable Bond Count8
Exact Mass453.031 Da
Monoisotopic Mass453.031 Da
Topological Polar Surface Area283.000 Ų
Heavy Atom Count27
Formal Charge0
Complexity165.000
Isotope Atom Count0
Defined Atom Stereocenter Count8
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Citations of This Product
Referencias
1. Chunxia Zhu, Yang Liu, Xiaojun Ji, Yaxuan Si, Xianhao Tao, Xiaohua Zhang, Lifang Yin.  (2024)  Enhanced Antitumor Efficacy of Cytarabine and Idarubicin in Acute Myeloid Leukemia Using Liposomal Formulation: In Vitro and In Vivo Studies.  Pharmaceutics,  16  (9): (1220).  [PMID:39339256] [10.3390/pharmaceutics16091220]
2. Liu Wei, Li Muyi, Zhang Pengli, Jiang Hongmei, Liu Wenjun, Guan Jinyu, Sun Yanhua, Liu Xiaoying, Zeng Qiongyao.  (2024)  One-step growth of Cu-doped carbon dots in amino-modified carbon nanotube–modified electrodes for sensitive electrochemical detection of BPA.  MICROCHIMICA ACTA,  191  (6): (1-11).  [PMID:38714599] [10.1007/s00604-024-06344-x]
3. Qinyu Luo, Zehua Wu, Yihang Pan, Yan Zhang.  (2025)  Disulfiram inhibits bacterial growth by inducing zinc-dependent reactive oxygen species.  Frontiers in Microbiology,      [PMID:40746315] [10.3389/fmicb.2025.1619416]
4. Guozhi Zhao, Fan Guo, Wenhui Yan, Ying Qu, Chongzheng Yan, Huaiyou Lv, Genju Li, Jianxiong Zhao, Hanmiao Xie, Yizhe Li, Tingting Tian, Zhongxi Zhao.  (2025)  A thermosensitive hydrogel with synergistic stromal targeting and antitumor immunity modulation for pancreatic cancer immunotherapy.  Materials Today Bio,      [PMID:40496724] [10.1016/j.mtbio.2025.101882]
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