Skip to Content
Merck
All Photos(1)

Documents

193739

Sigma-Aldrich

1-Indanol

98%

Synonym(s):

(±)-1-Indanol, (±)-1-Hydroxyindan

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

About This Item

Empirical Formula (Hill Notation):
C9H10O
CAS Number:
6351-10-6
Molecular Weight:
134.18
Beilstein:
2042960
EC Number:
228-755-3
MDL number:
MFCD00003797
UNSPSC Code:
12352100
PubChem Substance ID:
24851607
NACRES:
NA.22

Assay

98%

form

solid

bp

128 °C/12 mmHg (lit.)

mp

50-54 °C (lit.)

SMILES string

OC1CCc2ccccc12

InChI

1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2

InChI key

YIAPLDFPUUJILH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Chiral-sensitive aggregation of 1-indanol has been studied by FTIR spectroscopy. Transfer dehydrogenation of 1-indanol has been investigated over heterogeneous palladium catalyst using cyclohexene as hydrogen acceptor.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

Acute Tox. 4 Oral - 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

Jonas Altnöder et al.
Physical chemistry chemical physics : PCCP, 15(25), 10167-10180 (2013-05-15)
The aggregation behavior of racemic and enantiopure 1-indanol has been studied by FTIR spectroscopy, resonant ion dip IR spectroscopy, and spontaneous Raman scattering in supersonic jets. This triple experimental approach, augmented by homology to related molecular fragments and dispersion-corrected DFT
Wanda Mączka et al.
Molecules (Basel, Switzerland), 24(23) (2019-12-01)
The main purpose of this publication was to obtain the S-enantiomer of indan-1-ol with high enantiomeric excess and satisfactory yield. In our research, we used carrot callus cultures (Daucuscarota L.), whereby the enzymatic system reduced indan-1-one and oxidized indan-1-ol. During
Selective transfer dehydrogenation of aromatic alcohols on supported palladium.
Keresszegi C, et al.
New. J. Chem., 25(9), 1163-1167 (2001)
Ticiane C de Souza et al.
Bioprocess and biosystems engineering, 43(12), 2253-2268 (2020-07-30)
In this study, the modulation of enzymatic biocatalysts were developed by the use of lipase B from Candida antarctica covalently immobilized on an eco-friendly support, cashew apple bagasse, activated with 10% glycidol-ethylenediamine-glutaraldehyde (GEG) under different immobilization strategies (5 mM or 100 mM
Gustaf Götmar et al.
Analytical chemistry, 76(1), 197-202 (2003-12-31)
The distributions of the adsorption energies (AED) of two enantiomers, (R)-1- indanol and (S)-1-indanol, on a chiral stationary phase were measured and the results are discussed. The chiral phase used is made of cellulose tribenzoate coated on porous silica. The
View All Related Papers

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