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Sigma-Aldrich

1,5-Pentanediol

purum, ≥97.0% (GC)

Synonym(s):

Pentamethylene glycol

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About This Item

Linear Formula:
HO(CH2)5OH
CAS Number:
Molecular Weight:
104.15
Beilstein:
1560130
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

<0.01 mmHg ( 20 °C)

Quality Level

grade

purum

Assay

≥97.0% (GC)

form

liquid

autoignition temp.

635 °F

expl. lim.

13.2 %

refractive index

n20/D 1.450 (lit.)
n20/D 1.450

bp

242 °C (lit.)

density

0.994 g/mL at 25 °C (lit.)

SMILES string

OCCCCCO

InChI

1S/C5H12O2/c6-4-2-1-3-5-7/h6-7H,1-5H2

InChI key

ALQSHHUCVQOPAS-UHFFFAOYSA-N

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Application

1,5-Pentanediol can be used in a modified polyol process for the preparation of colloidal gold nanoparticles. It is also the starting material for preparing 1,5‐pentanediol dibenzoate.

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

287.6 °F - closed cup

Flash Point(C)

142 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yih Hong Lee et al.
Nature communications, 9(1), 2769-2769 (2018-07-19)
Organizing nanoparticles into supercrystals comprising multiple structures remains challenging. Here, we achieve one assembly with dual structures for Ag polyhedral building blocks, comprising truncated cubes, cuboctahedra, truncated octahedra, and octahedra. We create two micro-environments in a solvent evaporation-driven assembly system:
A Nanoreactor Framework of a Au@ SiO2 Yolk/Shell Structure for Catalytic Reduction of p?Nitrophenol.
Lee J, et al.
Advanced Materials, 20(8), 1523-1528 (2008)
Characterization of 1, 5?pentanediol dibenzoate as a potential ?green? plasticizer for poly (vinyl chloride).
Firlotte N, et al.
Journal of Vinyl & Additive Technology, 15(2), 99-107 (2009)
Hanne Evenbratt et al.
Acta dermato-venereologica, 89(2), 126-129 (2009-03-28)
The aim of this study was to compare pentane-1,5-diol and propane-1,2-diol used as absorption enhancers for cutaneously administered terbinafine. Fresh human skin samples were placed in a continuous flow diffusion cell with a gel containing terbinafine on top of the
David M Hunsicker et al.
Macromolecular rapid communications, 33(3), 232-236 (2011-12-17)
The Milstein catalyst has proven to be highly effective for the conversion of alcohols to esters, as well as alcohols and amines to amides and polyamides. We have recently found that the catalyst's range can be extended to very efficient

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