Phenyl glycidyl ether

Phenyl glycidyl ether
Names
	IUPAC name 2-(phenoxymethyl)oxirane
	Other names Phenyl glycidyl ether; Phenylglycidyl ether; Phenol glycidyl ether; Phenol-glycidaether; Phenoxypropene oxide; Phenoxypropylene oxide; Phenyl 2,3-epoxypropyl ether; Phenylglycydyl ether; Propane, 1,2-epoxy-3-phenoxy-; Oxirane, 2-(phenoxymethyl)-
Identifiers
CAS Number	122-60-1;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:82367;
ChEMBL	ChEMBL1568222;
ChemSpider	28958;
ECHA InfoCard	100.004.144
EC Number	204-557-2;
KEGG	C19291;
PubChem CID	31217;
RTECS number	TZ3675000;
UNII	44KJQ1655I;
UN number	2810
CompTox Dashboard (EPA)	DTXSID8021145 ;
	InChI InChI=1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2 Key: FQYUMYWMJTYZTK-UHFFFAOYSA-N;
	SMILES C1C(O1)COC2=CC=CC=C2;
Properties
Chemical formula	C9H10O2
Molar mass	150.177 g·mol−1
Melting point	3.5 °C (38.3 °F; 276.6 K)
Boiling point	245 °C (473 °F; 518 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H317, H332, H335, H341, H350, H412
Precautionary statements	P203, P261, P264, P271, P272, P273, P280, P281, P302+P352, P304+P340, P317, P318, P319, P321, P332+P317, P333+P313, P362+P364, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Phenyl glycidyl ether, is a liquid aromatic organic chemical in the glycidyl ether class of compounds.^[2] It has the formula C₉H₁₀O₂. It has the CAS Registry Number 122-60-1 and the IUPAC name of 2-(phenoxymethyl)oxirane. A key use is in the viscosity reduction of epoxy resin systems.^[3]^[4] It is REACH registered and on EINECS under the name 2,3-epoxypropyl phenyl ether.^[5]

^ "Phenyl glycidyl ether". pubchem.ncbi.nlm.nih.gov. Retrieved 1 June 2022.
^ Okumura, T. (1991). "retention indices of environmental chemicals on methyl silicone capillary column". Journal of Environmental Chemistry. 1 (2): 333–358. doi:10.5985/jec.1.333.
^ Jagtap, Ameya Rajendra; More, Aarti (2022-08-01). "Developments in reactive diluents: a review". Polymer Bulletin. 79 (8): 5667–5708. doi:10.1007/s00289-021-03808-5. ISSN 1436-2449. S2CID 235678040.
^ PubChem. "Phenyl glycidyl ether". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-05-31.
^ "Substance Information - ECHA". echa.europa.eu. Retrieved 2022-05-31.

[1] "Phenyl glycidyl ether". pubchem.ncbi.nlm.nih.gov. Retrieved 1 June 2022.

[2] Okumura, T. (1991). "retention indices of environmental chemicals on methyl silicone capillary column". Journal of Environmental Chemistry. 1 (2): 333–358. doi:10.5985/jec.1.333.

[3] Jagtap, Ameya Rajendra; More, Aarti (2022-08-01). "Developments in reactive diluents: a review". Polymer Bulletin. 79 (8): 5667–5708. doi:10.1007/s00289-021-03808-5. ISSN 1436-2449. S2CID 235678040.

[4] PubChem. "Phenyl glycidyl ether". pubchem.ncbi.nlm.nih.gov. Retrieved 2022-05-31.

[5] "Substance Information - ECHA". echa.europa.eu. Retrieved 2022-05-31.

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