127035
1-萘甲基胺
97%
别名:
1-(氨基甲基)萘, 1-萘甲胺
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关于此项目
线性分子式:
C10H7CH2NH2
化学文摘社编号:
分子量:
157.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-244-0
Beilstein/REAXYS Number:
2206459
MDL number:
Assay:
97%
Form:
liquid
产品名称
1-萘甲基胺, 97%
InChI key
NVSYANRBXPURRQ-UHFFFAOYSA-N
InChI
1S/C11H11N/c12-8-10-6-3-5-9-4-1-2-7-11(9)10/h1-7H,8,12H2
SMILES string
NCc1cccc2ccccc12
assay
97%
form
liquid
refractive index
n20/D 1.643 (lit.)
bp
290-293 °C (lit.)
density
1.073 g/mL at 25 °C (lit.)
functional group
amine
Quality Level
Gene Information
rat ... Adra2a(25083)
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Application
- 光致发光调控：一项研究表明了采用相分布（phase distribution）调节进行Ruddlesden-Popper 钙钛矿中光致发光的调控，揭示了其在光电设备中的潜在应用。1-萘甲基胺在材料性质的改善中起关键作用，改进了设备性能（Zhao et al., 2023）。
- 钙钛矿发光二极管：研究重点关注了通过超高真空退火实现的量子阱的二维尺寸剪裁（dimensional tailoring），以改善钙钛矿发光二极管的效率。该工艺采用1-萘甲基胺来改善夹层电学性质（interlayer electronic properties）和设备稳定性，为LED技术的进步带来重大贡献（Yu et al., 2020）。
General description
1-萘基甲胺可用作有机合成中的合成砌块，用于生产染料、色素和药物。
1-萘基甲胺增加聚[(4-羧酸苯基)乙炔]的诱导圆二色性(ICD)强度。.它与单甲氧基聚乙二醇琥珀酰亚胺碳酸酯 (mPEG-SC)反应生成氨基甲酸酯。
1-萘基甲胺增加聚[(4-羧酸苯基)乙炔]的诱导圆二色性(ICD)强度。.它与单甲氧基聚乙二醇琥珀酰亚胺碳酸酯 (mPEG-SC)反应生成氨基甲酸酯。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Susan D Van Arnum et al.
Journal of pharmaceutical and biomedical analysis, 50(2), 138-143 (2009-05-12)
An UV-HPLC method for the determination of the potency of mPEG-SC, 5 kDa (1) has been developed and validated. Validation acceptance criteria that is typical of small molecule method validation was successfully applied for this method. The method relies on
Kazuhide Morino et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 10(19), 4703-4707 (2004-09-17)
Poly[(4-carboxyphenyl)acetylene] (poly-1) exhibits an intense induced circular dichroism (ICD) in the UV-visible region upon complexation with excess (R)-1-(1-naphthyl)ethylamine ((R)-2), owing to the formation of a predominantly single-handed helical conformation of the polymer backbone. In the presence of a small amount
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