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111570

Sigma-Aldrich

3-Ethyl-3-pentanol

98%

Synonym(s):

Triethylcarbinol

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About This Item

Linear Formula:
(C2H5)3COH
CAS Number:
597-49-9
Molecular Weight:
116.20
Beilstein:
1731643
EC Number:
209-902-0
MDL number:
MFCD00004484
UNSPSC Code:
12352100
PubChem Substance ID:
24847034
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.430 (lit.)

bp

141 °C/743 mmHg (lit.)

density

0.824 g/mL at 25 °C (lit.)

SMILES string

CCC(O)(CC)CC

InChI

1S/C7H16O/c1-4-7(8,5-2)6-3/h8H,4-6H2,1-3H3

InChI key

XKIRHOWVQWCYBT-UHFFFAOYSA-N

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Application

3-Ethyl-3-pentanol was used to study the effect of alkanols on the micropolarity and microviscosity of the head group region, in the reverse micelles of AOT-heptane-water by fluorescence probing. 3-Ethyl-3-pentanols were encapsulated in the hexamers of resorcin[4]arenes.

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H226

Precautionary Statements

P210

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

100.4 °F - closed cup

Flash Point(C)

38 °C - closed cup

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’.

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Elsa Abuin et al.
Journal of colloid and interface science, 258(2), 363-366 (2003-03-06)
The effects of addition of alkanols (ethanol, n-hexanol, and 3-ethyl-3-pentanol) on the micropolarity and microviscosity of the head group region in reverse micelles of AOT-heptane-water have been investigated by fluorescence probing methods (ANS fluorescence yield and TMADPH fluorescence anisotropy), complemented
Raymond Behrendt et al.
Journal of peptide science : an official publication of the European Peptide Society, 21(8), 680-687 (2015-06-17)
Obtaining homogenous aspartyl-containing peptides via Fmoc/tBu chemistry is often an insurmountable obstacle. A generic solution for this issue utilising an optimised side-chain protection strategy that minimises aspartimide formation would therefore be most desirable. To this end, we developed the following
Sarit Slovak et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(27), 8515-8520 (2012-05-29)
After more than a century of research on resorcin[4]arenes (1) it is clear that such systems form spontaneously [1(6)(H(2)O)(8)]-type hexameric capsules in wet, non-polar, organic solvents. However, the interactions of these hexameric capsules with alcohols are far from being solved.

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