Chromotrope FB - Dye content,50% , CAS No.3567-69-9

CAS: 3567-69-9 Cat. No.: C121938 Molecular Weight: 502.43 EC Number: 222-657-4
AVAILABLE TO ORDER
GRADE & PURITY Dye content,50%
Synonyms
11959 Red | Eurocert Azorubine | Acid Brilliant Rubine A2G conc. | C.I. Acid Red 14, Disodium Salt | Crimson EMBL | Acid Chrome Blue BA-CF | Azo Rubine XX | Disodium 2-(4-sulfo-1-naphthylazo)-1-naphthol-4-sulfonate | Acetacid Red B | Hexacol Carmoisine |
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
10g
C121938-10g
10
$9.90
25g
C121938-25g
10
$10.90
50g
C121938-50g
7
$11.90
100g
C121938-100g
5
$12.90
500g
C121938-500g
2

$15.90

$23.90
Save $8.00 (33.47%)
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Why this grade

Dye content,50% 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 4 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

Application

Chromotrope FB has been used in indirect competitive CLIA (icCLIA) to detect its presence in foods

Specifications

Synonyms
11959 Red | Eurocert Azorubine | Acid Brilliant Rubine A2G conc. | C.I. Acid Red 14, Disodium Salt | Crimson EMBL | Acid Chrome Blue BA-CF | Azo Rubine XX | Disodium 2-(4-sulfo-1-naphthylazo)-1-naphthol-4-sulfonate | Acetacid Red B | Hexacol Carmoisine |
Specifications & Purity
Dye content, 50%
Biochemical and Physiological Mechanisms
Chromotrope FB, also known as acid red 14 (AR14), is a bright orange-red powder. It belongs to the class of monoazides. Chromotrope FB efficiently stains fatty substances and is also used to dye food and medicines
Storage
Room temperature
Shipped In
Normal
Names and Identifiers
Pubchem Sid488182525
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488182525
Canonical SmilesC1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)[O-])N=NC3=C(C4=CC=CC=C4C(=C3)S(=O)(=O)[O-])O.[Na+].[Na+]
IUPAC Namedisodium;4-hydroxy-3-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-1-sulfonate
InChIKeyYSVBPNGJESBVRM-UHFFFAOYSA-L
INCHI1S/C20H14N2O7S2.2Na/c23-20-15-8-4-3-7-14(15)19(31(27,28)29)11-17(20)22-21-16-9-10-18(30(24,25)26)13-6-2-1-5-12(13)16;;/h1-11,23H,(H,24,25,26)(H,27,28,29);;/q;2*+1/p-2
Isomeric SMILES C1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)[O-])N=NC3=C(C4=CC=CC=C4C(=C3)S(=O)(=O)[O-])O.[Na+].[Na+]
WGK Germany 2
RTECS QK1925000
Molecular Weight 502.43
Reaxy-Rn 4121348
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4121348&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
SuperclassBenzenoids
ClassNaphthalenes
SubclassNaphthalene sulfonic acids and derivatives
Intermediate Tree Nodes Naphthalene sulfonates
Direct Parent1-naphthalene sulfonates
Alternative Parents 1-naphthalene sulfonic acids and derivatives  1-sulfo,2-unsubstituted aromatic compounds  Phenoxides  Sulfonyls  Organosulfonic acids  Azo compounds  Propargyl-type 1,3-dipolar organic compounds  Organooxygen compounds  Organic sodium salts  Organic oxides  Hydrocarbon derivatives  Organic cations  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 1-naphthalene sulfonic acid or derivatives - 1-naphthalene sulfonate - Arylsulfonic acid or derivatives - 1-sulfo,2-unsubstituted aromatic compound - Phenoxide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Organosulfonic acid - Sulfonyl - Azo compound - Organic alkali metal salt - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic sodium salt - Organic nitrogen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic salt - Organic cation - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as 1-naphthalene sulfonates. These are organic aromatic compounds that contain a naphthalene moiety that carries a sulfonic acid group at the 1-position. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





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.

10 results found

Lot NumberCertificate TypeDateItem
E23151007Certificate of AnalysisApr 10, 2023 C121938
E2315203Certificate of AnalysisApr 10, 2023 C121938
E2315234Certificate of AnalysisApr 10, 2023 C121938
E2315240Certificate of AnalysisApr 10, 2023 C121938
E2315243Certificate of AnalysisApr 10, 2023 C121938
E2315244Certificate of AnalysisApr 10, 2023 C121938
E2315248Certificate of AnalysisApr 10, 2023 C121938
E2315251Certificate of AnalysisApr 10, 2023 C121938
E2315253Certificate of AnalysisApr 10, 2023 C121938
E2315999Certificate of AnalysisApr 10, 2023 C121938
Chemical and Physical Properties
SolubilitySoluble in water; Slightly soluble in Ethanol; Very slightly soluble in Acetone
Flash Point(°F)437.0 °F
Flash Point(°C)> 225 °C
Melt Point(°C)275 °C;λmax:383 nm,515 nm (2nd)
Molecular Weight502.400 g/mol
XLogP3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count9
Rotatable Bond Count2
Exact Mass501.988 Da
Monoisotopic Mass501.988 Da
Topological Polar Surface Area176.000 Ų
Heavy Atom Count33
Formal Charge0
Complexity854.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
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
References
1. Weijun Xie, Yue Zhang, Lei Xu, Dan Xie, Li Jiang, Yanmao Dong, Yan Yuan.  (2023)  Degradation of Organic Dyes by the UCNP/h-BN/TiO2 Ternary Photocatalyst.  ACS Omega,      [PMID:38162774] [10.1021/acsomega.3c01899]
2. Shen Shen, Huimin Li, Jia jia Fu, Hong Bo Wang.  (2022)  Wastewater purification with different precursors of carbon dots dominated titanium dioxide: Mechanism insight.  JOURNAL OF ALLOYS AND COMPOUNDS,      [PMID:] [10.1016/j.jallcom.2022.166162]
3. Zhaopeng Wang, Hui Lv, Yu Zhang, Yanan Li.  (2024)  A sensitive immunochromatography assay based on quantum dot nanobeads for determination of acid orange II.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2024.106485]
4. Xinmiao Xu, Yi Zhang, Yong Chen, Yu Liu.  (2024)  Vapor-Driven Crosslinked Hydroxypropyl-β-Cyclodextrin Electrospun Nanofibrous Membranes for Ultrafast Dye Removal.  Chemistry-Switzerland,  (4): (506-516).  [PMID:] [10.3390/chemistry6040029]
Solution Calculators
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