추천 제품
분석
>83.0% (HPLC)
Quality Level
양식
powder or crystals
mp
>300 °C (lit.)
응용 분야
diagnostic assay manufacturing
hematology
histology
저장 온도
room temp
SMILES string
[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 key
TXMRAEGWZZVGIH-UHFFFAOYSA-M
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신호어
Warning
유해 및 위험 성명서
예방조치 성명서
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
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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