Description

1-Amino-2-bromo-4-hydroxyanthraquinone (CAS No. 12217-92-4) is a high-purity anthraquinone derivative with the molecular formula C₁₄H₈BrNO₃. This compound, also known by its IUPAC name 1-amino-2-bromo-4-hydroxyanthracene-9,10-dione, is a versatile intermediate widely used in the synthesis of dyes, pigments, and specialty chemicals. Its distinct molecular structure, featuring an amino group, bromine substituent, and hydroxyl group on the anthraquinone backbone, enables precise functionalization for advanced applications.

Our product is rigorously tested for purity, stability, and consistency, making it ideal for research and industrial use. Available in various quantities, it is supplied with comprehensive analytical data (including HPLC, NMR, and MS) to ensure reproducibility. Suitable for organic synthesis, photochemical studies, and material science applications, this compound is handled under strict quality control to meet the demands of researchers and scientists.

Properties

• CAS Number: 12217-92-4
• Complexity: 413
• IUPAC Name: 1-amino-2-bromo-4-hydroxy-anthracene-9,10-dione
• InChI: InChI=1S/C14H8BrNO3/c15-8-5-9(17)10-11(12(8)16)14(19)7-4-2-1-3-6(7)13(10)18/h1-5,17H,16H2
• InChI Key: MSSQDESMUMSQEN-UHFFFAOYSA-N
• Exact Mass: 316.96876
• Molecular Formula: C14H8BrNO3
• Molecular Weight: 318.12
• SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)Br)N
• Topological: 80.4
• Monoisotopic Mass: 316.96876
• Synonyms: 1-Amino-2-bromo-4-hydroxyanthraquinone, Sumkaron Red 3B, Latyl Red B, 9,10-Anthracenedione, 1-amino-2-bromo-4-hydroxy-, Sandoplast Red 2B, Resiren Red T 3B, C.I. Disperse Violet 17, EINECS 204-160-4, 1-AMINO-2-BROMO-4-HYDROXY-9,10-ANTHRACENEDIONE, NSC 176660, BRN 1887275, DTXSID2059439, 4-14-00-00897 (Beilstein Handbook Reference), DTXCID6033378, 204-160-4, mssqdesmumsqen-uhfffaoysa-n, 116-82-5, Disperse Violet 17, 1-amino-2-bromo-4-hydroxyanthracene-9,10-dione, 1-Amino-2-bromo-4-hydroxy anthraquinone, 1-Amino-2-bromo-4-hydroxyanthrachinon, 1-Amino-2-bromo-4-hydroxy-9,10-anthraquinone, 1-Amino-2-brom-4-hydroxyanthrachinon, 12217-92-4, Anthraquinone, 1-amino-2-bromo-4-hydroxy-, 3251-92-1, 1-Amino-2-bromo-4-hydroxyanthraquinone, tech., C14H8BrNO3, 1-Amino-2-brom-4-hydroxyanthrachinon [Czech], MFCD00019156, 1-amino-2-bromo-4-hydroxy-anthraquinone, SCHEMBL2711627, 9, 1-amino-2-bromo-4-hydroxy-, 1-amino-2-bromo-4-hydroxy-9,10-dihydroanthracene-9,10-dione, NSC176660, AKOS001595018, FD32518, NSC-176660, WLN: L C666 BV IVJ DZ EE GQ, AC-10626, AS-15362, DISPERSE VIOLET 17 (LATYL RED B), DB-080700, EU-0069935, NS00020934, 1-Amino-2-bromo-4-hydroxyanthra-9,10-quinone #, 9,10-Anthracenedione,4-amino-2-bromo-1-hydroxy-, A803680, SR-01000080157, SR-01000080157-1, 1-azanyl-2-bromanyl-4-oxidanyl-anthracene-9,10-dione, Latyl Red B;1-Amino-2-bromo-4-hydroxy-9,10-anthraquinone

Application

1-Amino-2-bromo-4-hydroxyanthraquinone is primarily used as a key intermediate in the synthesis of anthraquinone-based dyes and pigments, particularly for textile and industrial coloring. Its bromo and hydroxy groups make it a valuable precursor for functionalized dyes with enhanced lightfastness and chemical resistance. Researchers also explore its potential in photodynamic therapy and organic semiconductor development due to its electron-accepting properties. Additionally, it serves as a model compound in studies of anthraquinone reactivity and substitution patterns.

Safety and Hazards

GHS Hazard Statements

• H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]

Precautionary Statements

• P261, P272, P280, P302+P352, P321, P333+P317, P362+P364, and P501

Hazard Classes and Categories

• Skin Sens. 1 (100%)

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