76892
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-854-4
Beilstein/REAXYS Number:
1560130
MDL number:
Assay:
≥97.0% (GC)
Form:
liquid
InChI key
ALQSHHUCVQOPAS-UHFFFAOYSA-N
InChI
1S/C5H12O2/c6-4-2-1-3-5-7/h6-7H,1-5H2
SMILES string
OCCCCCO
vapor pressure
<0.01 mmHg ( 20 °C)
grade
purum
assay
≥97.0% (GC)
form
liquid
autoignition temp.
635 °F
expl. lim.
13.2 %
Quality Level
bp
242 °C (lit.)
density
0.994 g/mL at 25 °C (lit.)
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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
10 - Combustible liquids
wgk
WGK 1
flash_point_f
287.6 °F - closed cup
flash_point_c
142 °C - closed cup
ppe
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)
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)
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:
Ya-Chuan Kao et al.
ACS nano, 14(2), 2542-2552 (2020-02-13)
Successful translation of laboratory-based surface-enhanced Raman scattering (SERS) platforms to clinical applications requires multiplex and ultratrace detection of small biomarker molecules from a complex biofluid. However, these biomarker molecules generally exhibit low Raman scattering cross sections and do not possess
Keisuke Yoshida et al.
Chemical communications (Cambridge, England), 48(55), 6981-6983 (2012-06-07)
Highly chemo- and regioselective acylation of 2-aminopentane-1,5-diol derivatives has been achieved by organocatalysis. An acyl group can be chemoselectively introduced onto the sterically hindered secondary hydroxy group in the presence of the primary one by virtue of the molecular recognition
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