跳转至内容
Merck
CN

308153

N-丙基-1,3-丙二胺

99%

登录 查看组织和合同定价。

选择尺寸


关于此项目

线性分子式:
CH3CH2CH2NH(CH2)3NH2
化学文摘社编号:
分子量:
116.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
245-869-9
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

N-丙基-1,3-丙二胺, 99%

InChI key

OWKYZAGJTTTXOK-UHFFFAOYSA-N

InChI

1S/C6H16N2/c1-2-5-8-6-3-4-7/h8H,2-7H2,1H3

SMILES string

CCCNCCCN

assay

99%

form

liquid

refractive index

n20/D 1.4451 (lit.)

bp

169 °C (lit.)

density

0.841 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

Application

N-Propyl-1,3-propanediamine was used in the synthesis of 1-benzotriazolylmethyl-3-propylhexahydropyrimidine.

pictograms

FlameCorrosion

signalword

Danger

hcodes

Hazard Classifications

Flam. Liq. 3 - Skin Corr. 1B

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

129.2 °F - closed cup

flash_point_c

54 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Alan R Katritzky et al.
The Journal of organic chemistry, 67(9), 3115-3117 (2002-04-27)
1-Benzotriazolylmethyl-3-propylhexahydropyrimidine (1) and 1,3-bis(1H-1,2,3-benzotriazol-1-ylmethyl)-1,2,3,4-tetrahydroquinazoline (3) were readily prepared by reactions of N-propyl-1,3-propanediamine or 2-aminobenzylamine with benzotriazole and formaldehyde, respectively. Intermediate 1 reacted with alkyl and aryl Grignard reagents to produce N,N'-unsymmetrically substituted hexahydropyrimidines 2a,b in 90 and 92% yields, respectively.
Ahmed Salman et al.
Genes, 11(10) (2020-10-04)
In this study, we seek to exclude other pathophysiological mechanisms by which Frmd7 knock-down may cause Idiopathic Infantile Nystagmus (IIN) using the Frmd7.tm1a and Frmd7.tm1b murine models. We used a combination of genetic, histological and visual function techniques to characterize
C M Maragos et al.
Cancer research, 53(3), 564-568 (1993-02-01)
Cell-mediated antitumor effects have, in part, been attributed to the production of NO. Compounds which generate NO might, therefore, be useful in attenuating the growth of tumor cells. Six nitric oxide/nucleophile adducts that release NO spontaneously in solution were tested

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持