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Why this grade
Moligand™, ≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Storage & shipping
Protected from light,Store at -20°C,Argon charged Ships Ice chest + Ice pads 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview
CBQCA is a fluorescencent dye for quantitation of protein (Ex=488nm, Em=530 nm).
Specifications
Specifications & Purity
Moligand™, ≥97%
Storage
Protected from light, Store at -20°C, Argon charged
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade
Moligand™
Purity
≥97%
Names and Identifiers
| Canonical Smiles | C1=CC=C2C(=C1)C=C(C(=N2)C=O)C(=O)C3=CC=C(C=C3)C(=O)O |
|---|---|
| IUPAC Name | 4-(2-formylquinoline-3-carbonyl)benzoic acid |
| InChIKey | MWNLTKCQHFZFHN-UHFFFAOYSA-N |
| INCHI | 1S/C18H11NO4/c20-10-16-14(9-13-3-1-2-4-15(13)19-16)17(21)11-5-7-12(8-6-11)18(22)23/h1-10H,(H,22,23) |
| Isomeric SMILES | C1=CC=C2C(=C1)C=C(C(=N2)C=O)C(=O)C3=CC=C(C=C3)C(=O)O |
| Molecular Weight | 305.28 |
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 →🔬 Specification Sheet
Full quality attributes and acceptance criteria for this grade.
View spec sheet →Advanced Data
Taxonomic Classification
Taxonomy Tree
- Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
- Class Quinolines and derivatives
- Subclass 4-aroylquinolines
- Class Quinolines and derivatives
- Superclass Organoheterocyclic compounds
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Quinolines and derivatives |
| Subclass | 4-aroylquinolines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | 4-aroylquinolines |
| Alternative Parents | 2-aroylquinolines Aryl-phenylketones Pyridinecarboxylic acids and derivatives Benzoic acids Pyridine carboxaldehydes Benzoyl derivatives Aryl-aldehydes Heteroaromatic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | 4-aroylquinoline - 2-aroylquinoline - Aryl-phenylketone - Benzoic acid or derivatives - Benzoic acid - Pyridine carboxylic acid or derivatives - Benzoyl - 2-pyridine carboxaldehyde - Aryl ketone - Aryl-aldehyde - Monocyclic benzene moiety - Pyridine - Benzenoid - Heteroaromatic compound - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Azacycle - Aldehyde - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as 4-aroylquinolines. These are compounds containing a quinoline which carries an aroyl group at the 4-position. An aroyl group is a univalent radical R-CO- derived from an aromatic carboxylic acid. |
| External Descriptors | quinolines - benzoic acids |
3D Structure
Interactive Chemical Structure Model
Certificates（CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Chemical and Physical Properties
| Sensitivity | Light sensitive |
|---|
Solution Calculators
Reviews
Customer Reviews
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