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线性分子式:
(CH3)2C6H3NH2
化学文摘社编号:
分子量:
121.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-437-4
Beilstein/REAXYS Number:
507414
MDL number:
产品名称
3,4-二甲基苯胺, 98%
InChI key
DOLQYFPDPKPQSS-UHFFFAOYSA-N
InChI
1S/C8H11N/c1-6-3-4-8(9)5-7(6)2/h3-5H,9H2,1-2H3
SMILES string
Cc1ccc(N)cc1C
assay
98%
bp
226 °C (lit.)
mp
49-51 °C (lit.)
solubility
H2O: slightly soluble
alcohol: soluble
Quality Level
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Application
3,4-二甲基苯胺(3,4-DMA)已被用于研究氯仿和二氯甲烷中2,3-二氰基-1,4-萘醌(DCNQ)与3,4-二甲基苯胺之间的电子供体-受体(EDA)相互作用 。它也可被用于在甲醇中与MoO(X)2(dtc)2(X = Cl或Br;dtc = 二乙基二硫代氨基甲酸酯)反应生成[MoNAr(dtc)3]2[Mo6O19]或MoNAr(dtc)3]4[Mo8O26]类离子亚胺配合物。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
新产品
此项目有
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
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
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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