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145025

Sigma-Aldrich

5-Amino-6-nitroquinoline

97%

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About This Item

Empirical Formula (Hill Notation):
C9H7N3O2
CAS Number:
35975-00-9
Molecular Weight:
189.17
EC Number:
252-822-6
MDL number:
MFCD00006798
UNSPSC Code:
12352100
PubChem Substance ID:
24848544
NACRES:
NA.22

Quality Level

100

Assay

97%

form

powder

mp

272-273 °C (dec.) (lit.)

functional group

nitro

SMILES string

Nc1c(ccc2ncccc12)[N+]([O-])=O

InChI

1S/C9H7N3O2/c10-9-6-2-1-5-11-7(6)3-4-8(9)12(13)14/h1-5H,10H2

InChI key

TYBYHEXFKFLRFT-UHFFFAOYSA-N

General description

Electrochemical reduction of 5-amino-6-nitroquinoline has been studied at carbon paste electrode by differential pulse voltammetry, direct current voltammetry, adsorptive stripping voltammetry and HPLC with electrochemical detection.

Application

5-Amino-6-nitroquinoline was used in preparation of imidazoquinoline derivatives.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ2101
STBJ0824
STBC0985V
STBC8616V
S70235

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J H Weisburger et al.
Environmental health perspectives, 67, 121-127 (1986-08-01)
Because mutagens typified by 2-amino-3-methylimidazo[4,5-f]quinoline (IQ) observed in cooked foods are widely consumed, detailed studies of their biochemical and biological properties including carcinogenicity are most important. IQ induces unscheduled DNA synthesis in liver cells, which when taken together with its
Determination of 5-amino-6-nitroquinoline at a carbon paste electrode.
Nemcova L, et al.
Collection of Czechoslovak Chemical Communications, 74(10), 1477-1488 (2009)

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