Esculin hydrate - ≥98% , CAS No.531-75-9

CAS: 531-75-9 Cat. No.: E107333 Peso molecular: 340.28(anhydrous) Beilstein Registry Number: 18(3/4)1326 Número EC: 208-517-5
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-hydroxy- | AKOS015895151 | SR-01000633930-1 | Z1494829512 | aesculin | CAS-531-75-9 | 7-hydroxy-2-oxo-2H-chromen-6-yl beta-D-glucopyranoside | C09264 | DTXCID5025318 | 7-hydroxy-6-(((2S,3R,4S,5S,6R)-3,
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
E107333-1g
5

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
5g
E107333-5g
4

23,90US$

35,90US$
Guardar 12,00 US$ (33.43%)
25g
E107333-25g
3

86,90US$

130,90US$
Guardar 44,00 US$ (33.61%)
100g
E107333-100g
1

320,90US$

481,90US$
Guardar 161,00 US$ (33.41%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Room temperature 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 7 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Product Introduction

Esculin hydrate has vasoprotective and venotonic properties.


Application

Esculin hydrate has been used as a component of sporulation-inducing esculin agar. It has also been used for esculin uptake assay.

Specifications

Sinónimos
2H-1-Benzopyran-2-one, 6-(beta-D-glucopyranosyloxy)-7-hydroxy- | AKOS015895151 | SR-01000633930-1 | Z1494829512 | aesculin | CAS-531-75-9 | 7-hydroxy-2-oxo-2H-chromen-6-yl beta-D-glucopyranoside | C09264 | DTXCID5025318 | 7-hydroxy-6-(((2S, 3R, 4S, 5S, 6R)-3,
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Antioxidant and plant coumarin glucoside. Exerts SOD-mimetic effects and reduces superoxide radicals generation. Inhibitory effects of chemically induced oxidative DNA damage and carcinogenesis in vivo.
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Nota
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488195236
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488195236
Sonrisas canónicasC1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O
IUPAC Name7-hydroxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one
InChIKeyXHCADAYNFIFUHF-TVKJYDDYSA-N
INCHI1S/C15H16O9/c16-5-10-12(19)13(20)14(21)15(24-10)23-9-3-6-1-2-11(18)22-8(6)4-7(9)17/h1-4,10,12-17,19-21H,5H2/t10-,12-,13+,14-,15-/m1/s1
Isómeros SMILES C1=CC(=O)OC2=CC(=C(C=C21)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O
RTECS DJ3085000
Peso molecular 340.28(anhydrous)
Beilstein 18(3/4)1326
Reaxy-Rn 1297608
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1297608&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
SuperclassPhenylpropanoids and polyketides
ClaseCoumarins and derivatives
SubclassCoumarin glycosides
Intermediate Tree Nodes Not available
Direct ParentCoumarin glycosides
Alternative Parents Phenolic glycosides  7-hydroxycoumarins  Hexoses  O-glycosyl compounds  1-benzopyrans  Pyranones and derivatives  1-hydroxy-2-unsubstituted benzenoids  Oxanes  Heteroaromatic compounds  Lactones  Secondary alcohols  Oxacyclic compounds  Acetals  Polyols  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Coumarin o-glycoside - Coumarin-6-o-glycoside - Phenolic glycoside - 7-hydroxycoumarin - Hydroxycoumarin - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Benzopyran - 1-benzopyran - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - Pyran - Monosaccharide - Oxane - Benzenoid - Heteroaromatic compound - Secondary alcohol - Lactone - Acetal - Oxacycle - Organoheterocyclic compound - Polyol - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Alcohol - Primary alcohol - Organooxygen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as coumarin glycosides. These are aromatic compounds containing a carbohydrate moiety glycosidically bound to a coumarin moiety.
External Descriptors coumarins
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
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ALOX15B Tchem Arachidonate 15-lipoxygenase, type II (7244 Activities)
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quadruplex DNA (2700 Activities)
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Mecanismos de acción
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.

16 results found

Lot NumberCertificate TypeFechaArticulo
F2626003Certificate of AnalysisJul 01, 2026 E107333
L2213132Certificate of AnalysisJun 04, 2026 E107333
L2213143Certificate of AnalysisJun 04, 2026 E107333
L2213161Certificate of AnalysisJun 04, 2026 E107333
L2213163Certificate of AnalysisJun 04, 2026 E107333
L2213173Certificate of AnalysisJun 04, 2026 E107333
L2213342Certificate of AnalysisJun 04, 2026 E107333
L2213356Certificate of AnalysisJun 04, 2026 E107333
L2213378Certificate of AnalysisJun 04, 2026 E107333
A2604101Certificate of AnalysisJan 06, 2026 E107333
J2109261Certificate of AnalysisJul 10, 2025 E107333
J2109262Certificate of AnalysisJul 10, 2025 E107333
J2109311Certificate of AnalysisJul 10, 2025 E107333
J2109312Certificate of AnalysisJul 10, 2025 E107333
C1922108Certificate of AnalysisJan 12, 2023 E107333
D2610074Certificate of AnalysisOct 20, 2022 E107333

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Propiedades químicas y físicas
Rotación específica [α]-79 ° (C=2.4, 50% Dioxane)
Punto de fusión (°C)203-205°C
Peso molecular340.280 g/mol
XLogP3-0.600
Hydrogen Bond Donor Count5
Hydrogen Bond Acceptor Count9
Rotatable Bond Count3
Exact Mass340.079 Da
Monoisotopic Mass340.079 Da
Topological Polar Surface Area146.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity495.000
Isotope Atom Count0
Defined Atom Stereocenter Count5
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Yin Lu, Yuan Zhang, Kan Zhang.  (2022)  Renewable biomass resources to access halogen- and phosphorus-free flame retardant thermosets with ultra-low heat release capacity.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2022.137670]
2. Lizhen Chen, Jie Wu, Feng Yan, Huangxian Ju.  (2020)  A facile strategy for quantitative sensing of glycans on cell surface using organic electrochemical transistors.  BIOSENSORS & BIOELECTRONICS,      [PMID:33298337] [10.1016/j.bios.2020.112878]
3. Yuanyang Dong, Qihang Hou, Meng Sun, Jingjing Sun, Bingkun Zhang.  (2020)  Targeted Isolation of Antioxidant Constituents from Plantago asiatica L. and In Vitro Activity Assay.  MOLECULES,  25  (8): (1825).  [PMID:32316264] [10.3390/molecules25081825]
4. Le Zhang, Ruiyang Ma, Shuangju Song, Weihua Liu, Qiuhua Wu, Zhi Wang.  (2025)  A natural esculin-based hydroxyl functionalized polymer for efficient enrichment of diamide insecticides residues in water, rice and soil samples.  FOOD CHEMISTRY,      [PMID:40633171] [10.1016/j.foodchem.2025.145341]
5. Yong-Yu Yang, Jing-Jing Qi, Si-Yi Jiang, Ling Ye.  (2023)  Esculin ameliorates obesity-induced insulin resistance by improving adipose tissue remodeling and activating the IRS1/PI3K/AKT/GLUT4 pathway.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:37778516] [10.1016/j.jep.2023.117251]
6. Jiangwei Ni, Ge Li, Ningfeng Dai, Zijiao Quan, Haibin Tong, Yu Liu.  (2023)  Esculin alleviates LPS-induced acute lung injury via inhibiting neutrophil recruitment and migration.  INTERNATIONAL IMMUNOPHARMACOLOGY,      [PMID:37068336] [10.1016/j.intimp.2023.110177]
7. Jinxia Liu, Xinyi Liu, Zhaoqing Song, Wenying Cao, Yue Li, Mingyu Xia, Dong Wang.  (2025)  A novel α-amylase from Streptococcus thermophilus 17140 with β-glycosidic bond hydrolysis capability for the transformation of rare ginsenosides.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:40024403] [10.1016/j.ijbiomac.2025.141621]
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