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126373

Sigma-Aldrich

3,4-Dimethylaniline

98%

Sinonimo/i:

3,4-Xylidine, 4-Amino-1,2-dimethylbenzene, 4-Amino-o-xylene

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About This Item

Formula condensata:
(CH3)2C6H3NH2
Numero CAS:
95-64-7
Peso molecolare:
121.18
Beilstein:
507414
Numero CE:
202-437-4
Numero MDL:
MFCD00007810
Codice UNSPSC:
12352100
ID PubChem:
24847724
NACRES:
NA.22

Saggio

98%

P. eboll.

226 °C (lit.)

Punto di fusione

49-51 °C (lit.)

Solubilità

H2O: slightly soluble
alcohol: soluble

Stringa SMILE

Cc1ccc(N)cc1C

InChI

1S/C8H11N/c1-6-3-4-8(9)5-7(6)2/h3-5H,9H2,1-2H3
DOLQYFPDPKPQSS-UHFFFAOYSA-N

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Categorie correlate

Applicazioni

3,4-Dimethylaniline (3,4-DMA) has been used to study the electron donor-acceptor (EDA) interaction between 2,3-dicyano-1,4-naphthoquinone (DCNQ) and 3,4-dimethylaniline, in chloroform and dichloromethane. It can also be used for reactions with MoO(X)2(dtc)2 (X = Cl or Br; dtc = diethyldithiocarbamate) in methanol to form ionic imido complexes of the type [MoNAr(dtc)3]2[Mo6O19] or MoNAr(dtc)3]4[Mo8O26].

Avvertenze

Danger

Indicazioni di pericolo

H301 + H311 + H331,H373,H411

Classi di pericolo

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

Codice della classe di stoccaggio

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

224.6 °F - closed cup

Punto d’infiammabilità (°C)

107 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
STBC2232V
STBB7653V
STBB7653
STBB2405
02719KA

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Martin Minelli et al.
Inorganic chemistry, 41(23), 5954-5960 (2002-11-12)
Anilines with alkyl substituents on the phenyl ring (ArNH2 = 2,4,6-trimethylaniline; 2,3-, 2,4-, 2,6-, and 3,4-dimethylaniline; and 2,6-diisopropylaniline) react with MoO(X)2(dtc)2 (X = Cl or Br; dtc = diethyldithiocarbamate) in methanol in the presence of 2 equiv of triethylamine to
Gururaj M Neelgund et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(1), 480-487 (2010-12-15)
The electron donor-acceptor (EDA) interaction between 2,3-dicyano-1,4-naphthoquinone (DCNQ) and 3,4-dimethylaniline (3,4-DMA) is studied in chloroform, dichloromethane and 1:1 (v/v) mixture of chloroform and dichloromethane. The rate of formation of the product was measured as a function of time using UV-vis
Akito Takeuchi et al.
Journal of occupational health, 53(3), 230-233 (2011-03-23)
The purpose of this research was to develop a determination method for xylidines (XLDs) in workplace air for risk assessment. The characteristics of the proposed method, such as recovery, detection limit, reproducibility, and storage stability of the samples were examined.
Tetyana Kobets et al.
Mutation research, 844, 10-24 (2019-07-22)
DNA-damaging activities of twenty-four structurally diverse unsubstituted and substituted cyclic compounds were assessed in embryo-fetal chicken livers. Formation of DNA adducts and strand breaks were measured using the nucleotide 32P-postlabelling (NPL) and comet assays, respectively. Unsubstituted monocyclic benzene, polycyclic fused
Robert J Strife et al.
Journal of chromatography. A, 1216(41), 6970-6973 (2009-09-08)
The assessment of human exposure to specific isomers of dimethylanilines (DMA's) is of interest for the evaluation of potential exposure-health outcome relationships. Improved analytical methods will help in identifying the environmental sources of such exposures. The separation of all six
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