Skip to Content
Merck
All Photos(1)

Key Documents

335924

Sigma-Aldrich

1-Piperidinepropionic acid

96%

Synonym(s):

3-Piperidin-1-ylpropionic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H15NO2
CAS Number:
Molecular Weight:
157.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

bp

105-108 °C/0.5 mmHg (lit.)

mp

105-110 °C (lit.)

SMILES string

OC(=O)CCN1CCCCC1

InChI

1S/C8H15NO2/c10-8(11)4-7-9-5-2-1-3-6-9/h1-7H2,(H,10,11)

InChI key

LPDGWMLCUHULJF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

1-Piperidinepropionic acid is an amino acid and its effectiveness as plasticizer has been tested.

Application

Reactant for synthesis of:
Protease activated receptor 2 agonists
Selective 5-HT6 antagonists
Kinesin Eg5 inhibitors
Selective ketone histone deacetylase inhibitors
JNK2 and JNK3 inhibitors
Opioid receptor antagonists

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Peter J Lillford et al.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 357(1423), 945-951 (2002-08-13)
Ice can be anything from a highly destructive agent in agriculture to a useful building material. Established industries are based on the known rules of physics and chemistry which allow some control of amounts of ice or ice crystal geometry.
Antigenic mimicry between piperazine derivatives and Wuchereria bancrofti microfilariae.
T Hussain et al.
Acta tropica, 50(4), 353-356 (1992-04-01)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service