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About This Item
Linear Formula:
C6H5OCH2CH(OH)CH3
CAS Number:
Molecular Weight:
152.19
Beilstein:
1941356
EC Number:
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:
NACRES:
NA.21
Quality Level
Assay
≥93%
impurities
<7% di(propylene glycol) phenyl ether
refractive index
n20/D 1.523 (lit.)
bp
243 °C (lit.)
solubility
water: soluble 198 g/L at 20 °C
density
1.064 g/mL at 20 °C (lit.)
functional group
hydroxyl
phenoxy
SMILES string
CC(O)COc1ccccc1
InChI
1S/C9H12O2/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3
InChI key
IBLKWZIFZMJLFL-UHFFFAOYSA-N
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General description
1-Phenoxy-2-propanol (PP), a gycol ether, can be synthesized by reacting propylene oxide with phenol in the presence of Al2O3-MgO/Fe3O4 catalyst. The influence of its anesthetic property on gastropods has been analyzed. Its degradation by microorganisms in different soil types has been investigated.
Application
1-Phenoxy-2-propanol has been used as an additive to saline to induce anesthetic effect on the peripheral tissues isolated from Biomphalaria alexandrina prior to fixation.
Legal Information
DOWANOL is a registered trademark of The Dow Chemical Company or an affiliated company of Dow
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Oded Halevi et al.
Scientific reports, 6, 36786-36786 (2016-11-11)
We present an all-additive manufacturing method that is performed at mild conditions, for the formation of organic single crystals at specific locations, without any photolithography prefabrication process. The method is composed of two steps; inkjet printing of a confinement frame
A Magnetically Separable Catalyst for Synthesis of 1-Phenoxy-2-propanol Via Atom-economic Reaction.
Feng S, et al.
J. Chin. Chem. Soc., 61(10), 1084-1088 (2014)
J Greenman
Microbios, 39(156), 101-108 (1984-01-01)
Propionibacterium acnes was grown in continuous culture in the presence of propylene phenoxetol. At sub-lethal concentrations of this antimicrobial agent (0.025-0.1% w/v) steady-state growth conditions were achieved. In comparison with the control, cell biomass, maximum specific growth rates and levels
I K Hegna et al.
Annales de l'Institut Pasteur. Microbiology, 139(4), 473-483 (1988-07-01)
The bactericidal and fungicidal effects of five disinfectants and one combination of two disinfectants were tested using a modified Kelsey-Sykes method in which living microorganisms suspended in a sterilized yeast suspension ("dirty" conditions) and in sterile distilled water ("clean" conditions)
Biodegradation of glycol ethers in soil.
Gonsior SJ and West RJ.
Environmental Toxicology and Chemistry / Setac, 14(8), 1273-1279 (1995)
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