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456063

Sigma-Aldrich

Bromaminic acid sodium salt

Synonym(s):

1-Amino-4-bromo-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid sodium salt

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About This Item

Empirical Formula (Hill Notation):
C14H7BrNNaO5S
CAS Number:
6258-06-6
Molecular Weight:
404.17
EC Number:
228-391-5
MDL number:
MFCD00019160
UNSPSC Code:
12171500
PubChem Substance ID:
24869107
NACRES:
NA.47

Assay

>83.0% (HPLC)

form

powder or crystals

mp

>300 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

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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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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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
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
Li Fan et al.
Huan jing ke xue= Huanjing kexue, 29(9), 2618-2623 (2008-12-17)
A bacterial strain that could degrade bromoamine acid (BAA) as the sole carbon source was isolated. It was identified as Sphingomonas sp. based on 16S rRNA gene sequence analysis and physio-biochemical characteristics. Under the optimal growth conditions, with temperature of
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
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.
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