Összes fotó(2)
Fontos dokumentumok
D39800
1,10-Dibromodecane
97%
Szinonimák:
Decamethylene dibromide
Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez
Összes fotó(2)
About This Item
Javasolt termékek
Minőségi szint
Teszt
97%
Forma
crystals
törésmutató
n20/D 1.4912 (lit.)
bp
160 °C/15 mmHg (lit.)
mp
25-27 °C (lit.)
sűrűség
1.335 g/mL at 25 °C (lit.)
SMILES string
BrCCCCCCCCCCBr
InChI
1S/C10H20Br2/c11-9-7-5-3-1-2-4-6-8-10-12/h1-10H2
Nemzetközi kémiai azonosító kulcs
GTQHJCOHNAFHRE-UHFFFAOYSA-N
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Általános leírás
1,10-Dibromodecane, also known as Decamethylene dibromide, is an aromatic and aliphatic monomer, often utilized in the polymerization reaction to synthesize high molecular weight polysulfides through polycondensation.
Alkalmazás
1,10-Dibromodecane is used:
- as a reactant in the Wurtz-type reaction during the synthesis of polyethylene
- Construction of pillar[4]arene[1]quinone-1,10-dibromodecane pseudorotaxanes in solution and in the solid state.: This research highlights the application of 1,10-Dibromodecane in constructing complex molecular structures known as pseudorotaxanes. The study focuses on the synthesis and stabilization of these structures both in solution and solid states, providing a foundational technique for developing advanced materials in chemical engineering, pharmaceutical synthesis, and high-performance materials within industrial chemical manufacturing sectors. This breakthrough offers potential pathways for new drug delivery systems and smart materials based on the unique properties of these supramolecular assemblies (Sheng et al., 2020).
Tárolási osztály kódja
11 - Combustible Solids
WGK
WGK 3
Lobbanási pont (F)
233.6 °F - closed cup
Lobbanási pont (C)
112 °C - closed cup
Egyéni védőeszköz
Eyeshields, Gloves, type N95 (US)
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Synthesis of polysulfides containing s-triazine rings from 6-substituted amino-1, 3, 5-triazine-2, 4-dithiols and 1, 10-dibromodecane
Macromolecular Rapid Communications, 20, 294-298 (1999)
Advanced healthcare materials, 9(14), e2000394-e2000394 (2020-06-17)
The complexity of biological systems poses a great challenge in the development of nanotheranostic agents with enhanced therapeutic efficacies. To systematically overcome a series of barriers during in vivo administration and achieve optimal antitumor activity, nanotheranostic agents that can self-adaptively
The journal of physical chemistry. B, 124(24), 5079-5090 (2020-05-28)
Conjugation-break flexible spacers in-between π-conjugated segments were utilized herein toward processable perylene diimide (PDI)-based polymers. Aromatic-aliphatic PDI-based polymers were developed via the two-phase polyetherification of a phenol-difunctional PDI monomer and aliphatic dibromides. These polyethers showed excellent solubility and film-forming ability
Chemical structures, properties, and applications of selected crude oil-based and bio-based polymers
Polymers, 14, 5551-5551 (2022)
Design and Synthesis of Imidazolium-Mediated Tro?ger?s Base-Containing Ionene Polymers for Advanced CO2 Separation Membranes
ACS Omega, 4, 3439-3448 (2019)
Tudóscsoportunk valamennyi kutatási területen rendelkezik tapasztalattal, beleértve az élettudományt, az anyagtudományt, a kémiai szintézist, a kromatográfiát, az analitikát és még sok más területet.
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