Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

534587

Sigma-Aldrich

(S)-(+)-2-Amino-1-pentanol

97%

Synonym(s):

L-Norvalinol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
CH3(CH2)2CH(NH2)CH2OH
CAS Number:
22724-81-8
Molecular Weight:
103.16
MDL number:
MFCD02683229
UNSPSC Code:
12352116
PubChem Substance ID:
24878048
NACRES:
NA.22

Assay

97%

optical activity

[α]20/D +17°, c = 1 in chloroform

mp

44-48 °C (lit.)

functional group

amine
hydroxyl

SMILES string

CCC[C@H](N)CO

InChI

1S/C5H13NO/c1-2-3-5(6)4-7/h5,7H,2-4,6H2,1H3/t5-/m0/s1

InChI key

ULAXUFGARZZKTK-YFKPBYRVSA-N

Application

(S)-(+)-2-Amino-1-pentanol can be used:
  • As a model compound in the study of estimation of dilution enthalpies of (R)-(−)-2-amino-1-pentanol in DMSO+H2O mixtures using isothermal titration calorimeter.
  • As a substrate to prepare tricyclic heterocyclic compounds as possible antagonists of corticotropin-releasing factor-1.
  • As an intermediate in one of the key synthetic steps for the preparation of an antiviral agent telaprevir.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

213.8 °F - closed cup

Flash Point(C)

101 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCP8415
MKBJ1918V
02706HJ
14124KH
08211DE

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Pairwise interaction enthalpies of enantiomers of β-amino alcohols in DMSO+ H2O mixtures at 298.15 K
Liang H, et al.
Chirality, 24(5), 374-385 (2012)
Ugi and Passerini reactions of biocatalytically derived chiral aldehydes: application to the synthesis of bicyclic pyrrolidines and of antiviral agent telaprevir
Moni L, et al.
The Journal of Organic Chemistry, 80(7), 3411-3428 (2015)
Design and synthesis of tricyclic corticotropin-releasing factor-1 antagonists
Gross RS, et al.
Journal of Medicinal Chemistry, 48(18), 5780-5793 (2005)

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