추천 제품
일반 설명
3,5-Dimethylaniline is the reagent commonly useful in the manufacture of dyes. It undergoes polymerization in the presence of cerium(IV) sulfate as an oxidant.
애플리케이션
3,5-Dimethylaniline was used in the synthesis of chiral packing materials for high performance liquid chromatography.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flash Point (°F)
215.1 °F - closed cup
Flash Point (°C)
101.7 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Chemical preparation of polyaniline and its derivatives by using cerium (IV) sulfate.
Synt. Metals, 69(1), 151-152 (1995)
The enantiomeric recognition of dihydropyrimidonic compounds by chiral selectors derived from 4-or 2-chloro-3, 5-dinitrobenzoic acid.
Tetrahedron Asymmetry, 16(6), 1175-1182 (2005)
Chemistry (Weinheim an der Bergstrasse, Germany), 24(45), 11771-11778 (2018-05-29)
Fluorous organic building blocks were utilized to develop two self-assembled, hydrophobic, fluorinated porous organic polymers (FPOPs), namely, FPOP-100 and FPOP-101. Comprehensive mechanical analyses of these functionalised triazine network polymers marked the introduction of mechanical stiffness among all porous organic network
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
Toxicological sciences : an official journal of the Society of Toxicology, 141(1), 300-313 (2014-06-29)
Epidemiological studies have demonstrated extensive human exposure to the monocyclic aromatic amines, particularly to 3,5-dimethylaniline, and found an association between exposure to these compounds and risk for bladder cancer. Little is known about molecular mechanisms that might lead to the
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