Malachite Green
Name: Malachite Green
CAS Registry Number: 569-64-2
CA Index Name: Methanaminium, N-[4-[[4-(dimethy-lamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-N-methyl-, chloride (1:1)
Other Names: C.I. Basic Green 4; Methanaminium, N-[4-[[4-(dimethylamino)phenyl]phenylmethylene]-2,5-cyclohexadien-1-ylidene]-N-methyl-, chloride; Victoria Green WB; ADC Malachite Green Crystals; Acryl Brilliant Green B; Aizen Malachite Green; Aizen Malachite Green Crystals; Aizen Malachite Green Liquid; Aniline Green; Astra Malachite Green; Astra Malachite Green B; Astra Malachite Green BXX; Atlantic Malachite Green; Basacryl Green X-BF; Basic Green 4; Basonyl Green 830; Basonyl Green NB 832; Benzal Green; Benzaldehyde Green; Bronze Green Toner A 8002; Burma Green B; C.I. 42000; Calcozine Green V; China Green; Diabasic Malachite Green; Diamond Green B; Diamond Green B Extra; Diamond Green BX; Diamond Green P Extra; Green MX; Green Malaquite; Grenoble Green; Hidaco Malachite Green Base; Hidaco Malachite Green LC; Hidaco Malachite Green SC; LC 6220; Light Green N; Lincoln Green Toner B 15-2900; Malachite Green 4; Malachite Green A; Malachite Green AN; Malachite Green B; Malachite Green CP; Malachite Green Crystals; Malachite Green Crystals BPC; Malachite Green J 3E; Malachite Green Powder; Malachite Green WS; Mala- chite Green XLS; Malachite Lake Green A; Malachite Green; Malachite Green Chloride; Mitsui Malachite Green; New Victoria Green Extra I; New Victoria Green Extra II; New Victoria Green Extra O; Oji Malachite Green; Solid Green Crystals O; Solid Green O; Super Ick Cure; Tertrophene Green M; Tokyo Aniline Malachite Green; Verona Basic Green M; Victoria Green; Victoria Green (basic dye); Victoria Green B; Victoria Green S; Victoria Green WPB
Merck Index Number: 5699
Chemical / Dye Class: Triphenylmethane
Molecular Formula: C23H25ClN2
Molecular Weight: 364.91
Physical Form: Green crystals with metallic luster
Solubility: Very soluble in water; soluble in ethanol, methanol, amyl alcohol
Melting Point: 112-114 °C
pH Range: 0.0-2.0; 11.6-14.0
Color Change at pH: Yellow (0.0) to green (2.0); green (11.6) to colorless (14.0)
pKa: 6.90
Absorption (λmax): 614 nm, 425 nm
Synthesis: Synthetic methods
Staining Applications: Antigens; antibodies; bacteria; bone cement; collagen; oxidized regenerated cellulose; alginates; chitosans; galactomannans; glycosaminoglycans; erythroblast; nucleic acids; peptides; proteins; skin
Biological Applications: Antiseptic formulation; detecting nucleic acids; early diagnosis of tuberculosis; identifying mammal genes; treating cancers, fungal diseases, pulmonary tuberculosis; medical device
Industrial Applications: Color filters; light-emitting devices; liquid crystal displays; optical recording materials; photoresists; inks; highlighters; toners; printed circuit board; photographic materials; adhesives; textiles
Safety / Toxicity: Acute toxicity; chronic toxicity; carcinogenicity; cytotoxicity; genotoxicity; mitochondrial toxicity; mutagenicity; nucleic acid damage
Металлоорганические соединения переходных элементов В книге рассмотрен один из самостоятельных разделов элементоорганической химии, ...
Fundamentals of Bioorganic Chemistry The texlbook is based on modern organic chemistry and considers the structure and chemical transformations of organic compounds, especially those that ...
Окиси олефинов и их производные Книга представляет собой монографию, посвящённую а-окисям олефинов и их ...
Монотерпеноиды в химии оптически активных феромонов насекомых Предлагаемая монография посвящена раскрытию синтетического потенциала ...