추천 제품
vapor density
3.01 (vs air)
Quality Level
분석
99%
양식
liquid
expl. lim.
22 %
refractive index
n20/D 1.411 (lit.)
bp
104 °C (lit.)
mp
−50 °C (lit.)
density
0.752 g/mL at 25 °C (lit.)
작용기
amine
SMILES string
CCCCCN
InChI
1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3
InChI key
DPBLXKKOBLCELK-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Amylamine can be used in the imidization of 2,6-dibromonaphthalene and 2,3,6,7-tetrabromonaphthalene bisanhydride, which are used to synthesize polybromo naphthalenetetracarboxylic acid diimides (NDIs).
It can be also be used to synthesize:
It can be also be used to synthesize:
- N
- -pentyl side chains of a cyclic heptapeptoid which forms the core of verticilide
- N-pentyl sulfamides from sulfamate salts.
Amylamine is a general reagent used in functionalizing the target molecules with pentyl chain. It has also been used as a cosurfactant to increase the phase stability of the bilayer systems.
주의사항
May darken in storage.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point (°F)
44.6 °F
Flash Point (°C)
7 °C
개인 보호 장비
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
이미 열람한 고객
Synthesis of nanosized silver platelets in octylamine-water bilayer systems.
Yener D O, et al.
Langmuir, 18(22), 8692-8699 (2002)
Microwave-mediated synthesis of a cyclic heptapeptoid through consecutive Ugi reactions
Barreto AS and Andrade CZ
Tetrahedron, 74(48), 6861-6865 (2018)
Investigations on the 4-quinolone-3-carboxylic acid motif. 7. Synthesis and pharmacological evaluation of 4-quinolone-3-carboxamides and 4-hydroxy-2-quinolone-3-carboxamides as high affinity cannabinoid receptor 2 (CB2R) ligands with improved aqueous solubility.
Mugnaini C, et al.
Journal of Medicinal Chemistry, 59(3), 1052-1067 (2016)
Efficient Synthesis of 5H-Cyclopenta [c] quinoline Derivatives via Palladium-Catalyzed Domino Reactions of o-Alkynylhalobenzene with Amine.
Luo Y, et al.
Organic Letters, 13(5), 1150-1153 (2011)
Tetrathiafulvalene in a perylene-3, 4: 9, 10-bis (dicarboximide)-based dyad: a new reversible fluorescence-redox dependent molecular system.
Leroy-Lhez S, et al.
The Journal of Organic Chemistry, 70(16), 6313-6320 (2005)
프로토콜
Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine
Global Trade Item Number
SKU | GTIN |
---|---|
171409-50ML | 4061838750907 |
171409-250ML | 4061837506413 |
171409-25ML | 4061838750891 |
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