Basic Violet 2 CAS 3248-91-7
Introduction：Basic information about Basic Violet 2 CAS 3248-91-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Basic Violet 2 Basic information
| Product Name: | Basic Violet 2 |
| Synonyms: | 4-[(4-Amino-3-methylphenyl)-(4-imino-3-methyl-1-cyclohexa-2,5-dienylidene)methyl]-2-methylaniline hydrochloride;Benzenamine, 4-((4-amino-3-methylphenyl)(4-imino-3-methyl-2,5-cyclohexadien-1-ylidene)methyl)- 2-methyl-, monohydrochloride;C.I.Basic Violet 24;Isorubin;New Fuchsin [for BiocheMical Research];NEW FUCHSIN (C.I. 42520) FOR MICROSCOPY;New fuchsin (C.I. 42520) for microscopy Certistain;Basic Violet 2, FuchsinN, Magenta(R) III |
| CAS: | 3248-91-7 |
| MF: | C22H24ClN3 |
| MW: | 365.91 |
| EINECS: | 221-831-7 |
| Product Categories: | |
| Mol File: | 3248-91-7.mol |
Basic Violet 2 Chemical Properties
| Boiling point | 300℃[at 101 325 Pa] |
| bulk density | 450kg/m3 |
| density | 0.692[at 20℃] |
| vapor pressure | 0Pa at 25℃ |
| storage temp. | Store at +5°C to +30°C. |
| solubility | 10g/l |
| form | Crystals or Crystalline Powder |
| Colour Index | 42520 |
| color | Dark green |
| PH | 3-4 (10g/l, H2O, 20℃) |
| Water Solubility | 20g/L |
| λmax | 553 nm |
| BRN | 8740867 |
| Stability: | Stable. Incompatible with strong oxidizing agents. |
| Major Application | diagnostic assay manufacturing hematology histology |
| Cosmetics Ingredients Functions | HAIR DYEING COLORANT |
| InChI | 1S/C22H24N3.ClH/c1-13-10-16(4-7-19(13)23)22(17-5-8-20(24)14(2)11-17)18-6-9-21(25)15(3)12-18;/h4-12H,23-25H2,1-3H3;1H/q+1;/p-1 |
| InChIKey | ORDGVBRMUJCHEO-UHFFFAOYSA-M |
| LogP | 1.537 |
| CAS DataBase Reference | 3248-91-7(CAS DataBase Reference) |
| EPA Substance Registry System | Benzenamine, 4,4'-[(4-imino-3-methyl-2,5-cyclohexadien-1-ylidene)methylene]bis[2-methyl-, hydrochloride (1:1) (3248-91-7) |
Safety Information
| Hazard Codes | Xn,Xi,N,T |
| Risk Statements | 36/37/38-40-36-50/53 |
| Safety Statements | 26-36/37-24/25-61-60 |
| RIDADR | UN 3077 9 / PGIII |
| WGK Germany | 3 |
| RTECS | CX9825000 |
| TSCA | TSCA listed |
| HS Code | 32041300 |
| Storage Class | 6.1C - Combustible, acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
| Hazard Classifications | Aquatic Acute 1 Aquatic Chronic 1 Carc. 1B Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
| Chemical Properties | solid | ||||||||||||||||||||||||||||||
| Uses | Textiles and leather industries, red dye, pharmaceutical. | ||||||||||||||||||||||||||||||
| Definition | ChEBI: A hydrochloride that is the monohydrochloride of 4-[(4-aminophenyl)(4-iminocyclohexa-2,5-dien-1-ylidene)methyl]-2-methylaniline. One of the minor constituents of Basic fuchsin, together with pararosanilin, rosanilin and magenta II. | ||||||||||||||||||||||||||||||
| Preparation | Commonly known as the New Magenta. 4 – (4-Amino-3-methylbenzyl)-2-methylbenzenamine with O-Methylaniline its hydrochloride salt is heated in the presence of an oxidizing agent. | ||||||||||||||||||||||||||||||
| General Description | The dry dye New fuchsin (C.I. 42520) for microscopy Certistain?, is used for the preparation of a staining solution that can be used for staining of histological tissue sections or other samples of human origin according to Ziehl-Neelsen, Gram staining as well as in combination with Schiff′s reagent. As a Certistain? dye it is chemically quality-certified according to highest standards and strict specifications. New fuchsin belongs to the group of triaminotriphenylmethane dyes. The dye is used in Ziehl-Neelsen and Gram staining as well as for methods with Schiff′s reagent. The cell wall of acid-fast bacteria (AFB) has a high proportion of wax and lipids and hence absorbs dyes only very slowly. As a measure to enhance the absorption of the fuchsin dye and thus the formation of the mycolate-fuchsin complex in the cell wall, the carbolfuchsin solution applied to the specimen is normally heated to evaporation point. If the Kinyoun carbolfuchsin solution is used, the heating of the solution is dispensable. Consequently, the release of hazardous phenolic vapors will be avoided. Once the AFB have absorbed the fuchsin dye, it is virtually impossible to decolorize them again, even when they are intensively treated with a decolorizing solution such as e. g. hydrochloric acid in ethanol. Accordingly, AFB are termed as acid- and alcohol-fast for staining, and are stained red in the microscopic visualization. Correspondingly, all non-acid-fast microorganisms are counterstained with an appropriate dye. Pretreatment of the specimens with Sputofluol? dissolves the bacteria from the surrounding viscid sputum and cell material. Sputofluol? also has a disinfectant effect, with the result that any microorganisms that are present are killed off. It is registered as IVD and certified as CE product. For more details, please see instructions for use (IFU). The IFU can be downloaded from this webpage. | ||||||||||||||||||||||||||||||
| Hazard | Possible carcinogen. | ||||||||||||||||||||||||||||||
| Flammability and Explosibility | Not classified | ||||||||||||||||||||||||||||||
| Properties and Applications | dark red light purple. Soluble in water and ethanol is red. The strong sulfuric acid for yellow until golden brown, diluted into light yellow. Dyes to join sodium hydroxide solution appears orange brown precipitation.
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Basic Violet 2 Preparation Products And Raw materials
| Raw materials | 4,4'-DIAMINO-3,3'-DIMETHYLDIPHENYLMETHANE-->o-Toluidine |
