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Merck

16230

Sigma-Aldrich

4-Bromanilin

≥99.0% (GC)

Synonym(e):

1-Amino-4-bromobenzene, p-Bromoaniline

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About This Item

Lineare Formel:
BrC6H4NH2
CAS-Nummer:
Molekulargewicht:
172.02
Beilstein:
742031
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

≥99.0% (GC)

Form

solid

mp (Schmelzpunkt)

56-62 °C (lit.)
63-65 °C

Löslichkeit

ethanol: soluble 0.5 g/10 mL, clear, colorless to almost colorless

Funktionelle Gruppe

bromo

SMILES String

Nc1ccc(Br)cc1

InChI

1S/C6H6BrN/c7-5-1-3-6(8)4-2-5/h1-4H,8H2

InChIKey

WDFQBORIUYODSI-UHFFFAOYSA-N

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Allgemeine Beschreibung

Photocatalytic degradation of 4-bromoaniline over ZnO or TiO2 (anatase and rutile) has been investigated in a photocatalytic reactor.

Anwendung

4-Bromoaniline was used as carbon and nitrogen supplement in the culture medium of Moraxella sp. strain G.

Biochem./physiol. Wirkung

4-Bromoaniline reduces gluconeogenesis in renal cortical slices obtained from the kidneys of untreated, male Fischer 344 rats.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

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Mohammad Hossein Habibi et al.
Annali di chimica, 94(5-6), 421-428 (2004-07-29)
Photocatalytic degradation of aqueous solution of aniline derivatives such as ortho-nitroaniline (ONA), meta-nitroaniline (MNA), para-nitroaniline (PNA), 4-bromoaniline (4-BrA) and 2-chloroaniline (2-ClA) were carried out over ZnO or TiO2 (anatase and rutile) in a photocatalytic reactor. The observed results revealed that
J Zeyer et al.
Applied and environmental microbiology, 50(2), 447-453 (1985-08-01)
Moraxella sp. strain G is able to utilize as sole source of carbon and nitrogen aniline, 4-fluoroaniline, 2-chloroaniline, 3-chloroaniline, 4-chloroaniline (PCA), and 4-bromoaniline but not 4-iodoaniline, 4-methylaniline, 4-methoxyaniline, or 3,4-dichloroaniline. The generation time on PCA was 6 h. The pathway
Fernanda Raphael Escobar Gimenes et al.
PloS one, 15(11), e0241849-e0241849 (2020-11-20)
To identify the types of nasogastric/nasoenteric tube (NGT/NET)-related adverse events and to analyze the degree of harm and the factors associated with mechanical device-related complications. A prospective cohort study was conducted from October 2017 to April 2019 in seven Brazilian
S K Hong et al.
Toxicology letters, 114(1-3), 125-133 (2000-03-14)
Haloanilines are widely used as chemical intermediates in the manufacture of pesticides, dyes and drugs. The purpose of this study was to examine the in vitro nephrotoxic effects of the four 4-haloaniline and four 3,5-dihaloaniline isomers using renal cortical slices
M C Roberts et al.
Equine veterinary journal, 11(4), 239-243 (1979-10-01)
The absorption of d-xylose forms the basis of a useful screening test in the investigation of small intestinal disorders in the horse. A comparison has been made of different assay methods and there was no significant difference between the results

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