Introduction：Basic information about Mordant Blue 29 CAS 1667-99-8, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Mordant Blue 29 Basic information
| Product Name: | Mordant Blue 29 |
| Synonyms: | Chrome Cyanine BLA;CHROME AZUROL S INDICATOR FOR METAL TITRATION;Chromium(Metal)Powder99%;CHROMAZUROL S (C.I. No 43825 );Chrome Azurol S, pure;Benzoic acid, 5-(3-carboxy-5-methyl-4-oxo-2,5-cyclohexadien-1-ylidene)(2,6-dichloro-3-sulfophenyl)methyl-2-hydroxy-3-methyl-, trisodium salt;ChomeazurolS;PolytropeblueB |
| CAS: | 1667-99-8 |
| MF: | C23H13Cl2Na3O9S |
| MW: | 605.28 |
| EINECS: | 216-787-0 |
| Product Categories: | Analytical Chemistry;Bipyridyls, etc. (Chelating Reagents);Chelating Reagents |
| Mol File: | 1667-99-8.mol |
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Mordant Blue 29 Chemical Properties
| storage temp. | room temp |
| solubility | water: 0.1% |
| pka | pK1:2.45;pK2:4.86;pK3:11.47 (25°C) |
| Colour Index | 43825 |
| form | Powder |
| color | Dark-brown |
| Odor | Odorless |
| Water Solubility | Soluble in water |
| ε(extinction coefficient) | ≥9000 at 424-436nm in H2O at 0.03g/L
≥9000 at 424-436nm in H2O |
| λmax | 458 nm |
| BRN | 4110655 |
| Stability: | Stable. Incompatible with strong oxidizing agents. |
| Major Application | diagnostic assay manufacturing
hematology
histology |
| InChIKey | FUIZKNBTOOKONL-NDOZRWCBSA-K |
| SMILES | C(=C1/C=C(C(=O)C(C([O-])=O)=C/1)C)(/C1=CC(=C(O)C(C([O-])=O)=C1)C)\C1C(Cl)=CC=C(S([O-])(=O)=O)C=1Cl.[Na+].[Na+].[Na+] |
| EPA Substance Registry System | Benzoic acid, 5-[(3-carboxy-5-methyl-4-oxo-2,5-cyclohexadien-1-ylidene)(2,6-dichloro-3-sulfophenyl)methyl]-2-hydroxy-3-methyl-, trisodium salt (1667-99-8) |
Safety Information
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 26-36 |
| WGK Germany | 3 |
| TSCA | TSCA listed |
| HS Code | 29189900 |
| Storage Class | 11 - Combustible Solids |
Mordant Blue 29 Usage And Synthesis
| Chemical Properties | dark brown powder |
| Uses | Chromeazurol S (cas# 1667-99-8) is a compound useful in organic synthesis.Dyes and metabolites. |
| Preparation | 2,4-Dichloro-3-formylbenzenesulfonic acid?and 2-Hydroxy-3-methylbenzoic acid condensation, its product oxidation and changed into sodium salt. |
| Properties and Applications | red light blue. Soluble in water for brown light yellow, slightly soluble in ethanol for red light brown. In concentrated sulfuric acid for hot magenta, after dilution to orange, and then generate a orange precipitation. Dye aqueous solution and sodium hydroxide as 3H-indol-3-one,2-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro- blue.
| Standard | Ironing Fastness | Light Fastness | Fulling | Persperation Fastness | Soaping | Water | | Alkali | Acid | | ISO | 4 | 3 | 4 | 2 | 4-5 | 4 | 5 | |
| Purification Methods | The crude phenolic triphenylmethanecarboxysulfonic acid triNa salt (40g) is dissolved in water (250mL) and filtered. Then conc HCl (50mL) is added to the filtrate, with stirring. The precipitate is filtered off, washed with HCl (2M) and dried. It is redissolved in water (250mL), and precipitation is repeated twice more in a water bath at 70o. It is dried under vacuum over solid KOH (first), then P2O5 [Martynov et al. Zh Analyt Khim 32 519 1977]. It has also been purified by paper chromatography using n-butanol, acetic acid and water (7:3:1). First and second spots were extracted. It chelates Al and Be. It is used also for estimating fluoride. [Beilstein 11 IV 707.] |
Mordant Blue 29 Preparation Products And Raw materials
| Raw materials | 2,4-Dichloro-3-formylbenzenesulfonic acid-->3-Methylsalicylic acid |
