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Merck
CN

D139505

4-(二甲氨基)苯甲腈

98%

别名:

4-氰基-N,N-二甲基苯胺, DMABN

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关于此项目

线性分子式:
(CH3)2NC6H4CN
化学文摘社编号:
分子量:
146.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-819-8
Beilstein/REAXYS Number:
971606
MDL number:
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产品名称

4-(二甲氨基)苯甲腈, 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-(二甲胺基)苄腈可用于合成3,6-二苯基-2,5-二氢-吡咯并[3,4-c]吡咯-1,4-二酮衍生物。

General description

4-(二甲胺基)苄腈在光激发下可以发生从二甲基氨基部分到氰基苯基部分的分子内电荷转移(ICT),导致出现双重荧光,因此,它被广泛用于光物理研究。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

存储类别

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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)
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
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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