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![二氢氧化1,3-二[4-(二甲氨基)苯基]-2,4-二羟基环丁烯二鎓二(内盐) Dye content 90 %](/deepweb/assets/sigmaaldrich/product/structures/301/519/500149b3-198c-44cf-b952-7e91f54fc48e/640/500149b3-198c-44cf-b952-7e91f54fc48e.png)
化驗
>83.0% (HPLC)
形狀
powder or crystals
mp
>300 °C (lit.)
應用
diagnostic assay manufacturing
hematology
histology
儲存溫度
room temp
SMILES 字串
[Na+].Nc1c(cc(Br)c2C(=O)c3ccccc3C(=O)c12)S([O-])(=O)=O
InChI
1S/C14H8BrNO5S.Na/c15-8-5-9(22(19,20)21)12(16)11-10(8)13(17)6-3-1-2-4-7(6)14(11)18;/h1-5H,16H2,(H,19,20,21);/q;+1/p-1
InChI 密鑰
TXMRAEGWZZVGIH-UHFFFAOYSA-M
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訊號詞
Warning
危險聲明
危險分類
Eye Irrit. 2
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Yuanyuan Qu et al.
FEMS microbiology letters, 246(1), 143-149 (2005-05-05)
Sphingomonas xenophaga QYY with the ability to degrade bromoamine acid (BAA) was previously isolated from sludge samples. The enhancement of BAA removal by strain QYY in sequencing batch reactors (SBRs) was investigated in this study. The results showed that augmented
Yuan-yuan Qu et al.
Applied biochemistry and biotechnology, 159(3), 664-672 (2009-01-14)
A combined biological (augmented membrane bioreactor (MBR)) and photochemical (photocatalysis and ozonation) treatment has been proposed for bromoamine acid (BAA) removal in dyeing wastewater. It was demonstrated that the color and chemical oxygen demand removal in the sequential augmented MBR
Wei Zhang et al.
Huan jing ke xue= Huanjing kexue, 30(10), 2930-2935 (2009-12-09)
Combined ALR-BAC was used to treat bromoamine acid wastewater. The results showed that the ALR system could run steadily for over 1 months at the BAA concentration 650 mg x L(-1) after one-month acclimation, the decoloration rate of BAA was
Yuanyuan Qu et al.
Biodegradation, 17(1), 83-91 (2006-02-03)
One high-effective bromoamine acid (1-amino-4-bromoanthraquinone-2-sulfonic acid, BAA) degrading strain was isolated previously with the ability to use BAA as sole source of carbon and nitrogen. It was identified as Sphingomonas xenophaga QYY by 16S rDNA sequence analysis and physio-biochemical tests.
Younis Baqi et al.
Organic letters, 9(7), 1271-1274 (2007-03-14)
[structure: see text]. The synthesis of anilinoanthraquinones 3a-z was achieved by a new, Cu(0)-catalyzed, microwave-assisted Ullmann coupling reaction of bromaminic acid (1) with aniline derivatives 2a-z in phosphate buffer. Good to excellent isolated yields were obtained within only 2-20 min
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