6-Bromo-2-naphthyl β-D-glucuronide - ≥95% , CAS No.22720-35-0

CAS: 22720-35-0 Cat. No.: B350143 Peso molecular: 399.2 Número EC: 245-176-1 PubChem CID: 89804
Disponible para pedir
GRADE & PURITY ≥95%
Synonyms
6-BROMO-2-NAPHTHYL-BETA-D-GLUCURONIDE | 6-Bromo-2-naphthyl beta-D-glucopyranosiduronic acid | 6-Bromo-2-naphthyl beta -D-glucuronide | AKOS027381737 | AS-11181 | (2S,3S,4S,5R,6S)-6-(6-bromonaphthalen-2-yloxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxyl
Storage
Store at -20°C
Shipped In
Ice chest + Ice pads
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5mg
B350143-5mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
58,90US$
25mg
B350143-25mg
3
224,90US$
50mg
B350143-50mg
3
282,90US$
250mg
B350143-250mg
3
1.112,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -20°C Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

6-Bromo-2-naphthyl β-D-glucuronide is a histochemical substrate for β-D-glucuronidase.

Specifications

Sinónimos
6-BROMO-2-NAPHTHYL-BETA-D-GLUCURONIDE | 6-Bromo-2-naphthyl beta-D-glucopyranosiduronic acid | 6-Bromo-2-naphthyl beta -D-glucuronide | AKOS027381737 | AS-11181 | (2S, 3S, 4S, 5R, 6S)-6-(6-bromonaphthalen-2-yloxy)-3, 4, 5-trihydroxytetrahydro-2H-pyran-2-carboxyl
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%
Nombres e identificadores
Sonrisas canónicasC1=CC2=C(C=CC(=C2)Br)C=C1OC3C(C(C(C(O3)C(=O)O)O)O)O
IUPAC Name(2S,3S,4S,5R,6S)-6-(6-bromonaphthalen-2-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
InChIKeyTYDGGWYIJKMLEO-JHZZJYKESA-N
INCHI1S/C16H15BrO7/c17-9-3-1-8-6-10(4-2-7(8)5-9)23-16-13(20)11(18)12(19)14(24-16)15(21)22/h1-6,11-14,16,18-20H,(H,21,22)/t11-,12-,13+,14-,16+/m0/s1
Isómeros SMILES C1=CC2=C(C=CC(=C2)Br)C=C1O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O
PubChem CID 89804
Peso molecular 399.2

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 Glycosyl compounds
Direct ParentPhenolic glycosides
Alternative Parents O-glucuronides  Hexoses  O-glycosyl compounds  Naphthalenes  Beta hydroxy acids and derivatives  Pyrans  Aryl bromides  Oxanes  Secondary alcohols  Acetals  Polyols  Oxacyclic compounds  Carboxylic acids  Monocarboxylic acids and derivatives  Organobromides  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Naphthalene - Beta-hydroxy acid - Aryl bromide - Aryl halide - Hydroxy acid - Monosaccharide - Benzenoid - Pyran - Oxane - Secondary alcohol - Organoheterocyclic compound - Acetal - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Polyol - Hydrocarbon derivative - Alcohol - Organic oxide - Organohalogen compound - Organobromide - Carbonyl group - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
External Descriptors Not available
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.

3 results found

Lot NumberCertificate TypeFechaArticulo
I2217264Certificate of AnalysisJul 18, 2025 B350143
I2217265Certificate of AnalysisJul 18, 2025 B350143
I2217266Certificate of AnalysisJul 18, 2025 B350143
Propiedades químicas y físicas
Peso molecular399.190 g/mol
XLogP32.000
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count7
Rotatable Bond Count3
Exact Mass398 Da
Monoisotopic Mass398 Da
Topological Polar Surface Area116.000 Ų
Heavy Atom Count24
Formal Charge0
Complexity462.000
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
Calculadoras de soluciones
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