物质信息
ID:321162
名称和标识
IUPAC传统名
3-(piperidin-1-yl)propan-1-amine
IUPAC标准名
3-(piperidin-1-yl)propan-1-amine
别名
3-哌啶丙胺3-PiperidinopropylamineN-(3-Aminopropyl)piperidine1-(3-氨丙基)哌啶
化合物性质
产品相关信息
Empirical Formula (Hill Notation)
C8H18N2
纯度
95%
安全信息
GHS危险品标识
腐蚀金属，类别1
腐蚀皮肤，类别1A，1B，1C
严重眼损伤，类别1
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
安全公开号
26-36/37/39-45
GHS警示词
Danger
联合国危险货物编号
2735
MSDS下载
GHS危险声明
H302-H314
RID/ADR
UN 2735 8/PG 3
个人保护装置
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS警示性声明
P280-P305+P351+P338-P310
联合国危险货物等级
8
联合国危险货物包装类别(PG)
3
欧盟危险性物质标志
腐蚀性 (C)危险公开号
22-34
德国WGK号
3
理化性质
闪点
179.6 °F
82 °C
密度
0.895 g/mL at 25 °C
折射率
n20/D 1.476
描述信息
包装
5 g in glass bottle
Application
Reactant for synthesis of:
• A chemotype that inhibits Botulinum neurotoxin serotype A light chain, P. falciparum Malaria, and Ebola filovirus1
• Membrane targeting antibiotics2
• 5-HT3A receptor antagonists3
• Histamine H3 antagonists4
• Berberine derivatives for stabilization of G-quadruplex DNA and down regulation of oncogene c-myc5Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity6
5 g in glass bottle
Application
Reactant for synthesis of:
• A chemotype that inhibits Botulinum neurotoxin serotype A light chain, P. falciparum Malaria, and Ebola filovirus1
• Membrane targeting antibiotics2
• 5-HT3A receptor antagonists3
• Histamine H3 antagonists4
• Berberine derivatives for stabilization of G-quadruplex DNA and down regulation of oncogene c-myc5Reactant for incorporation of basic side chains into cryptolepine scaffold for antimalarial activity6
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