Skip to Content
Merck
All Photos(2)

Documents

328413

Sigma-Aldrich

(R)-(−)-1-Indanol

99%

Synonym(s):

R(−)-1-Hydroxyindan

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Empirical Formula (Hill Notation):
C9H10O
CAS Number:
697-64-3
Molecular Weight:
134.18
Beilstein:
4350388
MDL number:
MFCD00064164
UNSPSC Code:
12352002
PubChem Substance ID:
24859734
NACRES:
NA.22

Assay

99%

optical activity

[α]30/D −29°, c = 2 in chloroform

mp

72-73 °C (lit.)

SMILES string

O[C@@H]1CCc2ccccc12

InChI

1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m1/s1

InChI key

YIAPLDFPUUJILH-SECBINFHSA-N

Gene Information

human ... UGT2B17(7367) , UGT2B7(7364)

Looking for similar products? Visit Product Comparison Guide

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

Katia Le Barbu-Debus et al.
Physical chemistry chemical physics : PCCP, 20(21), 14635-14646 (2018-05-18)
The influence of flexibility and hydrogen bond formation on the IR absorption and vibrational circular dichroism (VCD) spectrum of a floppy protic molecule, namely, (S)-1-indanol, is studied in both non-polar CCl4 and polar DMSO solvents. The experimental IR absorption and
J Reddy et al.
Applied microbiology and biotechnology, 51(5), 614-620 (1999-07-03)
Recombinant Escherichia coli cells expressing the toluene dioxygenase (TDO) genes from Pseudomonas putida convert indene to cis-1S,2R-indandiol, a potentially important intermediate for the chemical synthesis of the HIV-1 protease inhibitor, Crixivan. A bioconversion process was developed through optimization of medium
Attila Felinger et al.
Journal of chromatography. A, 1005(1-2), 35-49 (2003-08-20)
The inverse method of isotherm determination consists in calculating the numerical values of the coefficients of an isotherm model that give a set of chromatographic profiles in best possible agreement with the set of experimental profiles available. This method was
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
Dongmei Zhou et al.
Journal of chromatography. A, 1015(1-2), 73-87 (2003-10-23)
The competitive isotherm data for the enantiomers of 1-indanol were measured on three columns, a microbore column (15 cm x 0.1 cm), a conventional analytical column (15 cm x 0.46 cm), and a semi-preparative column (20 cm x 1.0 cm)
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