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1-Piperidinepropanol / 5 G

Purity: 97 %
Synonym: Piperidine-1-propanol; 3-piperidin-1-yl-propanol; 3-hydroxypropylpiperidine; 3-piperidin-1-ylpropan-1-ol; 1-(3-Hydroxypropyl)piperidine
Molecular Formula: C8H17NO
Molecular Weight: 143.23
SKU: MND-45639
CAS Number: 104-58-5
MDL number: MFCD00023781
EC Number: 203-216-5
Form: liquid
Note: Prices are for comparison only. Contact Sales for current pricing.
Packing size: 5 G  
112.70 EUR



Safety Information


Hazard Statements

H302
H315
H319
H335
H314
H302 + H312 + H332
H332
H312

Precautionary Statements

P280
P264
P270
P501
P305 + P351 + P338
P261
P271
P405
P302 + P352
P260
P362 + P364
P403 + P233
P301 + P330 + P331
P363
P304 + P340
P330
P321
P264 + P265
P319
P332 + P317
P337 + P317
P301 + P317
P317
P316

Pictograms



Properties

Signal WordWarning
Flash Point (C)97.8 °C - closed cup
Flash Point (F)208.0 °F - closed cup
Density0.944 g/mL at 25 °C (lit.)
Boiling Point94-95 °C/0.5 mmHg (lit.)

 Product Description

1-Piperidinepropanol is an organic compound with a piperidine ring attached to a propanol chain. It is commonly used as an intermediate in the synthesis of pharmaceuticals and fine chemicals.

 

Application

This compound is utilized in the production of various pharmaceuticals, serving as a building block in chemical synthesis processes.

 

 

Articles:

- Oculogyric crisis symptoms related to risperidone treatment: a case report

Publication Date: 24 November 2023

Tao Lv, Liping Wu, Longlong Li, Min Zhang, Qingyu Tan & Ping Liu

https://doi.org/10.1186/s12888-023-05379-3

 

- Comparison of the ex vivo receptor occupancy profile of ketamine to several NMDA receptor antagonists in mouse hippocampus

Publication Date: Available online 16 July 2013

Brian Lord, Cindy Wintmolders, Xavier Langlois, Leslie Nguyen, Tim Lovenberg, Pascal Bonaventure

https://doi.org/10.1016/j.ejphar.2013.06.028

 

- Synthesis and evaluation of N-alkyl-S-[3-(piperidin-1-yl)propyl]isothioureas: High affinity and human/rat species-selective histamine H3 receptor antagonists

Publication Date: Available online 26 September 2013

Shinya Harusawa, Koichi Sawada, Takuji Magata, Hiroki Yoneyama, Lisa Araki, Yoshihide Usami, Kouta Hatano, Kouichi Yamamoto, Daisuke Yamamoto, Atsushi Yamatodani

https://doi.org/10.1016/j.bmcl.2013.09.052