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Merck

76892

Sigma-Aldrich

1,5-Pentandiol

purum, ≥97.0% (GC)

Synonym(e):

Pentamethylenglykol

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About This Item

Lineare Formel:
HO(CH2)5OH
CAS-Nummer:
Molekulargewicht:
104.15
Beilstein:
1560130
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdruck

<0.01 mmHg ( 20 °C)

Qualitätsniveau

Qualität

purum

Assay

≥97.0% (GC)

Form

liquid

Selbstzündungstemp.

635 °F

Expl.-Gr.

13.2 %

Brechungsindex

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

bp

242 °C (lit.)

Dichte

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

InChIKey

ALQSHHUCVQOPAS-UHFFFAOYSA-N

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Anwendung

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.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

287.6 °F - closed cup

Flammpunkt (°C)

142 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves


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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)
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:
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Multi-resistance to antibiotic therapy and to biocides is becoming increasingly common, which has led to mounting concern worldwide regarding the future use of traditional antimicrobials. Diols or glycols also have antimicrobial effects. Pentane-1,5-diol has low oral toxicity, is essentially non-irritating
Wenjie Xu et al.
Chemical communications (Cambridge, England), 47(13), 3924-3926 (2011-02-25)
A new strategy was developed for the direct conversion of furfural to 1,5-pentanediol by the hydrogenolysis of the furan ring under mild conditions based on Pt/Co(2)AlO(4) catalyst. This is the first report of the direct catalytic conversion of furfural to

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