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Merck
CN

209864

4-叔丁基苯胺

99%

别名:

4-(1,1-二甲基乙基)苯胺, 4-叔丁基苯胺, 4-氨基-叔丁基苯, 对叔丁基苯胺, 对(叔丁基)苯胺

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关于此项目

线性分子式:
(CH3)3CC6H4NH2
化学文摘社编号:
分子量:
149.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-215-9
Beilstein/REAXYS Number:
2205786
MDL number:
Assay:
99%
Form:
liquid
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Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.538 (lit.)

bp

90-93 °C/3 mmHg (lit.)

mp

15-16 °C (lit.)

density

0.937 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)c1ccc(N)cc1

InChI

1S/C10H15N/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,11H2,1-3H3

InChI key

WRDWWAVNELMWAM-UHFFFAOYSA-N

General description

4-丁基苯胺和 4-丁基苯甲醛可以通过基质辅助激光解吸电离芯片系统在乙醇中发生席夫碱形成反应

Application

4-丁基苯胺用于合成:
  • 4-丁基-4′,4″-二硝基三苯胺,含二胺单体的新三苯胺
  • 2-氧嘧啶[4,5-d]嘧啶-5(6H)-酮


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Novel aromatic polyamides and polyimides functionalized with 4-tert-butyltriphenylamine groups.
Hsiao S-H, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(15), 4579-4592 (2006)
Self-complementary hydrogen bonding heterocycles designed for the enforced self-assembly into supramolecular macrocycles.
Marsh A, et al.
Chemical Communications (Cambridge, England), 13, 1527-1528 (1996)
Christopher G Thomson et al.
Bioorganic & medicinal chemistry letters, 21(14), 4281-4283 (2011-06-15)
A novel and robust synthesis of the fragment, 2-amino-5-tert-butylpyridine, has been described, which has been shown to have improved physicochemical properties over 4-tert-butylaniline, when considering drug-like properties. The synthesis also yields fragments containing more highly oxidised precursors to the tert-butyl



全球贸易项目编号

货号GTIN
209864-25G04061838770943
209864-5G04061838770950