추천 제품
분석
97%
형태
solid
mp
210 °C (dec.) (lit.)
SMILES string
[Br-].C[N+](C)(C)CCCBr
InChI
1S/C6H15BrN.BrH/c1-8(2,3)6-4-5-7;/h4-6H2,1-3H3;1H/q+1;/p-1
InChI key
NNZGNZHUGJAKKT-UHFFFAOYSA-M
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일반 설명
(3-Bromopropyl)trimethylammonium bromide is a quaternary ammonium salt and has various applications in organic chemistry, including the synthesis of hydrophilic-hydrophobic block copolymers. Additionally, this compound can be used as a surfactant in the synthesis of ultrathin nano scrolls (NSs).
애플리케이션
(3-Bromopropyl)trimethylammonium bromide can be used as a reagent in the synthesis of:
- Octa-cationic imidazolyl Al(III) phthalocyanine bifunctional catalyst CAT 2.
- Divalent surfactants like N-(3-trimethylammoniumpropyl)hexadecyldimethylammonium dibromide and N-(3-trimethylammoniumpropyl)octadecylammonium dibromide by reacting with surfactant precursor compounds hexadecyldimethylamine (C16NMe2), octadecyldimethylamine (C18NMe2) respectively.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
Analytical biochemistry, 145(1), 87-90 (1985-02-15)
Reduced lysozyme was alkylated with 3-bromopropyltrimethylammonium bromide to give reduced and S-3-(trimethylated amino)propylated lysozyme. It was soluble in a wide range of pH and is suitable as the protein substrate to determine protease specificity.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 19(1), 56-65 (2019-12-12)
A series of Cy5.5 dye analogs and targeted probes with net charges varied from -3 to 0 were synthesized by an optimized method, followed by comparing their spectral and photostability properties in saturated solutions of air, oxygen, and argon. The
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