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456063

Bromaminic acid sodium salt

Name: Bromaminic acid sodium salt
Brand: ALDRICH

别名:

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

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关于此项目

经验公式（希尔记法）:

C₁₄H₇BrNNaO₅S

化学文摘社编号:

6258-06-6

分子量:

404.17

NACRES:

NA.47

PubChem Substance ID:

24869107

UNSPSC Code:

12171500

EC Number:

228-391-5

MDL number:

MFCD00019160

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属性

assay

>83.0% (HPLC)

Quality Level

100

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

说明

pictograms

GHS07

signalword

Warning

hcodes

H319

pcodes

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Inactivation of yeast hexokinase by Cibacron Blue 3G-A: spectral, kinetic and structural investigations.

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

[Degradation characteristics of bromoamine acid by Sphingomonas sp. FL].

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

Rapid and efficient microwave-assisted copper(0)-catalyzed ullmann coupling reaction: general access to anilinoanthraquinone derivatives.

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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全球贸易项目编号

货号	GTIN
456063-25G	04061832339719