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456063

Sigma-Aldrich

Bromaminic acid sodium salt

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Synonym(s):
1-Amino-4-bromo-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid sodium salt
Empirical Formula (Hill Notation):
C14H7BrNNaO5S
CAS Number:
Molecular Weight:
404.17
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.47

assay

>83.0% (HPLC)

Quality Level

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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This Item
114367861367B1125
Bromaminic acid sodium salt

456063

Bromaminic acid sodium salt

Bromocresol Green sodium salt 90% (HPLC), ACS reagent, Dye content 90 %

114367

Bromocresol Green sodium salt

Thymol Blue sodium salt ACS reagent, Dye content 95 %

861367

Thymol Blue sodium salt

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

assay

>83.0% (HPLC)

assay

90% (HPLC)

assay

-

assay

7.2-9.1% dry basis (ICP)

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

mp

>300 °C (lit.)

mp

230 °C (dec.) (lit.)

mp

283-285 °C (dec.) (lit.)

mp

-

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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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
R N Puri et al.
The Biochemical journal, 300 ( Pt 1), 91-97 (1994-05-15)
Yeast hexokinase, a homodimer (100 kDa), is an important enzyme in the glycolytic pathway. Although Cibacron Blue 3G-A (Reactive Blue 2) has been previously shown to inactivate yeast hexokinase, no comprehensive study exists concerning the nature of interaction(s) between hexokinase

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