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About This Item
Linear Formula:
(CH3)2NC6H4CN
CAS Number:
Molecular Weight:
146.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-819-8
Beilstein/REAXYS Number:
971606
MDL number:
Assay:
98%
Form:
crystals
Product Name
4-(Dimethylamino)benzonitrile, 98%
InChI key
JYMNQRQQBJIMCV-UHFFFAOYSA-N
InChI
1S/C9H10N2/c1-11(2)9-5-3-8(7-10)4-6-9/h3-6H,1-2H3
SMILES string
CN(C)c1ccc(cc1)C#N
assay
98%
form
crystals
bp
318 °C (lit.)
mp
72-75 °C (lit.)
Quality Level
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Application
4-(Dimethylamino)benzonitrile can be used in the synthesis of 3,6-diphenyl-2,5-dihydro-pyrrolo[3,4-c]pyrrole-1,4-dione derivatives.
General description
4-(Dimethylamino)benzonitrile is extensively used in photophysical studies due to its ability to undergo intramolecular charge transfer (ICT) from the dimethylamino moiety to the cyanophenyl moiety on photo-excitation leading to the appearance of dual fluorescence.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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D Hesk et al.
Xenobiotica; the fate of foreign compounds in biological systems, 18(8), 955-966 (1988-08-01)
1. The metabolic fate of 4-cyanoacetanilide (CAA), labelled with 14C and 13C in the N-acetyl group, was studied in rats (oral dose, 22.5 mg/kg) and mice (oral dose 21.7 mg/kg). 2. The metabolic profile in the urine of rats was
D H Hutson et al.
Xenobiotica; the fate of foreign compounds in biological systems, 14(12), 925-934 (1984-12-01)
4-Cyano-N,N-dimethylaniline (CDA), when administered to rats as a single oral dose (18.5 mg/kg), was rapidly absorbed and eliminated as a mixture of metabolites in the urine (86% dose after 24 h). Residues in tissues after 48 h, expressed as microgram
Novel, soluble diphenyl-diketo-pyrrolopyrroles: Experimental and theoretical study.
Vala M, et al.
Dyes and Pigments, 84(2), 176-182 (2010)
Do fluorescence and transient absorption probe the same intramolecular charge transfer state of 4-(dimethylamino) benzonitrile?
Gustavsson T, et al.
J. Chem. Phys. , 131, 031101-031101 (2009)
C J Logan et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(5), 391-397 (1985-05-01)
4-Cyano-N,N-dimethylaniline (CDA), when administered as a single oral dose to mice (18.5 mg/kg), was rapidly absorbed and eliminated. The major route of elimination was the urine (78% dose in 24h). The residues in the tissues 48 h after dosing, as
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