추천 제품
Quality Level
분석
95%
형태
liquid
autoignition temp.
838 °F
포함
≤200 ppm BHT as inhibitor
refractive index
n20/D 1.53 (lit.)
bp
268-271 °C (lit.)
density
1.018 g/mL at 25 °C (lit.)
SMILES string
CC(=C)c1cccc(c1)C(C)(C)N=C=O
InChI
1S/C13H15NO/c1-10(2)11-6-5-7-12(8-11)13(3,4)14-9-15/h5-8H,1H2,2-4H3
InChI key
ZVEMLYIXBCTVOF-UHFFFAOYSA-N
일반 설명
3-Isopropenyl-α,α-dimethylbenzyl isocyanate (m-TMI) is a telechelic derivative that shows an α-unsaturation and has an isocyanate end group. It is majorly used in polymeric synthesis.
애플리케이션
m-TMI can be used as a tetrafunctional isocyanate which can further be used in the development of polymer electrolyte. It can be used as a coupling agent in the preparation of jute reinforced polypropylene.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 2 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Inhalation
표적 기관
Lungs
Storage Class Code
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
Flash Point (°F)
>212.0 °F - closed cup
Flash Point (°C)
> 100 °C - closed cup
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Unexpected alternating radical copolymerization of chlorotrifluoroethylene with 3-isopropenyl-alpha, alpha$?-dimethylbenzyl isocyanate
Journal of Polymer Science Part A: Polymer Chemistry, 48(12), 2681-2697 (2010)
Jute-polypropylene composites using m-TMI-grafted-polypropylene as a coupling agent
Materials & Design, 43(1), 112-117 (2013)
Novel carbamoyl phosphonate monomers and polymers from unsaturated isocyanates
Journal of Polymer Science Part A: Polymer Chemistry, 31(1), 239-247 (1993)
Copolymerization behavior of 3-isopropenyl-alpha, alpha-dimethylbenzylamine and a preliminary evaluation of the copolymers in thermoset coatings
Journal of Applied Polymer Science, 82(4), 1030-1039 (2001)
Journal of biomedical materials research, 23(3), 295-309 (1989-03-01)
A series of methacrylate oligomers containing pendant isocyanate groups were synthesized by reacting 2-isocyanatoethyl methacrylate (IEM) and/or m-isopropenyl-alpha, alpha-dimethylbenzyl isocyanate (TMI) in ethoxyethyl acetate with methacrylates ranging from methyl to stearyl methacrylate or allyl-, cyclohexyl-, glycidyl-, i-bornyl-, or dicyclopentenyloxyethyl methacrylate.
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