2-Ethylhexyl glycidyl ether supplier

Name
2-Ethylhexyl glycidyl ether
EINECS 219-553-6
CAS No. 2461-15-6
Article Data5
CAS DataBase
Density 0.913 g/cm³
Solubility <0.1 g/100 mL at 19 °C in water
Melting Point
Formula C₁₁H₂₂O₂
Boiling Point 259.452 °C at 760 mmHg
Molecular Weight 186.294
Flash Point 96.667 °C
Transport Information
Appearance colourless liquid
Safety 26-37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Oxirane,[[(2-ethylhexyl)oxy]methyl]- (9CI);Propane, 1,2-epoxy-3-[(2-ethylhexyl)oxy]-(6CI,7CI,8CI);1-(2-Ethylhexyloxy)-2,3-epoxypropane;Oxirane,2-[[(2-ethylhexyl)oxy]methyl]-;Adeka Glycilol ED 518;Adeka Glycilol ED 518S;Denacol EX 12;Denacol EX121;ED 518;Epiol EH;Epodil 746;Epodil 747;Glycidyl 2-ethylhexyl ether;Grilonit 1807-41;Heloxy 116;Heloxy MK 116;JX 014;Laproxid 301;NSC 252154;[[(2-Ethylhexyl)oxy]methyl]oxirane;
PSA 21.76000
LogP 2.61820

Synthetic route

: 37961-18-5
1-chloro-3-(2-ethyl-hexyloxy)-propan-2-ol

: 2461-15-6
2-ethyl-hexyl glycidyl ether

Conditions

Conditions	Yield
With potassium tert-butylate In tetrahydrofuran at 20 - 25℃; for 18h;

: 104-76-7
2-Ethylhexyl alcohol

: 106-89-8
epichlorohydrin

A: 2461-15-6
2-ethyl-hexyl glycidyl ether

B: 1,3-di(2-ethylhexyloxy)-2-propylglycidyl ether

C: 3-chloroprop-2-enylglycidyl ether

Conditions

Conditions	Yield
Stage #1: 2-Ethylhexyl alcohol With tetrabutylammomium bromide; sodium hydroxide at -40℃; for 0.5h; Inert atmosphere; Stage #2: epichlorohydrin at 80℃; for 12h; Reagent/catalyst; Temperature;

...Expand

: 104-76-7
2-Ethylhexyl alcohol

: 106-89-8
epichlorohydrin

: 2461-15-6
2-ethyl-hexyl glycidyl ether

Conditions

Conditions	Yield
Stage #1: 2-Ethylhexyl alcohol With tetrabutylammomium bromide; sodium hydroxide at -40℃; for 0.5h; Inert atmosphere; Stage #2: epichlorohydrin at 40℃; for 12h; Reagent/catalyst; Temperature;
Stage #1: 2-Ethylhexyl alcohol; epichlorohydrin With sulfuric acid; (3-chloro-2-hydroxypropyl)-2-ethylhexyl ether at 80 - 100℃; for 4h; Stage #2: With sodium hydroxide at 50℃; Stage #3: With sodium chloride; sodium hydroxide In water at 85 - 95℃; for 6h;	752.8 g

: 104-76-7
2-Ethylhexyl alcohol

: 106-89-8
epichlorohydrin

A: 2461-15-6
2-ethyl-hexyl glycidyl ether

B: 1,3-di(2-ethylhexyloxy)-2-propylglycidyl ether

Conditions

Conditions	Yield
Stage #1: 2-Ethylhexyl alcohol With tetrabutylammomium bromide; sodium hydroxide at -40℃; for 0.5h; Inert atmosphere; Stage #2: epichlorohydrin at 60℃; for 12h; Reagent/catalyst; Temperature;

...Expand

: 104-76-7
2-Ethylhexyl alcohol

: 106-89-8
epichlorohydrin

A: 2461-15-6
2-ethyl-hexyl glycidyl ether

B: 59068-03-0
5,13-diethyl-7,11-dioxa-9-heptadecanol

Conditions

Conditions	Yield
Stage #1: 2-Ethylhexyl alcohol With tetrabutylammomium bromide; sodium hydroxide at -40℃; for 0.5h; Inert atmosphere; Stage #2: epichlorohydrin at 40℃; for 12h; Reagent/catalyst; Temperature;

...Expand

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 70445-33-9
1-O-(2-ethylhexyl)glycerin

Conditions

Conditions	Yield
With formic acid; water; sodium hydroxide In Triethylene glycol dimethyl ether at 120℃; for 12h; Reagent/catalyst; Solvent;	98.5%
Stage #1: 2-ethyl-hexyl glycidyl ether With boron trifluoride diethyl etherate In acetone at 10 - 20℃; for 2.66667h; Stage #2: With methylamine In water; acetone at 10 - 20℃; for 0.166667h; Stage #3: With formic acid In water at 50 - 55℃; for 3h; Temperature; Reagent/catalyst;	89.1%
Stage #1: 2-ethyl-hexyl glycidyl ether With formic acid; sulfuric acid at 80 - 100℃; Stage #2: With methanol at 60℃; Stage #3: With water; sodium hydroxide Product distribution / selectivity;	78.1%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 5397-31-9
3-(2-ethylhexoxy)propylamine

: C33H69NO5

Conditions

Conditions	Yield
at 60 - 120℃; for 10.67h;	98%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 71242-04-1
2-(4-ethyl-2-oxaoctyl)thiirane

Conditions

Conditions	Yield
With thiourea In methanol for 48h; Ambient temperature;	97.4%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 124-38-9
carbon dioxide

: 4-(((2-ethylhexyl)oxy)methyl)-1,3-dioxolan-2-one

Conditions

Conditions	Yield
With tetrabutylammomium bromide at 110℃; under 7500.75 Torr; for 3h;	91%
With (2-aminoethyl)(4-(bis(2,6-dimethoxyphenyl)methylene)-3,5-dimethoxycyclohexa-2,5-dien-1-yl)diphenylphosphonium trifluoromethanesulfonate; sodium iodide In chlorobenzene at 100℃; under 760.051 Torr; for 12h; Schlenk technique;	91%
With C24H12N2O10(4-)*2Cu(2+); tetrabutylammomium bromide at 20℃; under 760.051 Torr; for 48h; Schlenk technique;	6%

: 104-75-6
2-Ethylhexylamine

: 2461-15-6
2-ethyl-hexyl glycidyl ether

poly(2-ethylhexylamine-co-2-ethylhexyl glycidyl ether): poly(2-ethylhexylamine-co-2-ethylhexyl glycidyl ether)

Conditions

Conditions	Yield
at 60 - 120℃; for 10.6667h;	90%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 201230-82-2
carbon monoxide

: 95-56-7
2-hydroxybromobenzene

: 1556674-22-6
3-(((2-ethylhexyl)oxy)methyl)-2H-benzo[e][1,4]dioxepin-5(3H)-one

Conditions

Conditions	Yield
With potassium phosphate; palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl In N,N-dimethyl-formamide at 100℃; under 3750.38 Torr; for 16h; Autoclave;	88%

...Expand

: 7617-74-5
3-(dodecyloxy)-1-propylamine

: 2461-15-6
2-ethyl-hexyl glycidyl ether

poly(2-ethylhexyl glycidyl ether-co-3-(dodecyloxy)-1-propylamine): poly(2-ethylhexyl glycidyl ether-co-3-(dodecyloxy)-1-propylamine)

Conditions

Conditions	Yield
at 60 - 120℃; for 10.6667h;	85%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 104-76-7
2-Ethylhexyl alcohol

: 59068-03-0
5,13-diethyl-7,11-dioxa-9-heptadecanol

Conditions

Conditions	Yield
sulfated zirconium oxide at 150℃; Inert atmosphere;	83.2%
With sodium hydride for 48h; Ambient temperature;	61%
With tetrabutylammomium bromide; sodium hydroxide at 60℃; Cooling with ice;

: 75-15-0
carbon disulfide

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 4-(4-ethyl-2-oxaoctyl)-1,3-dithiolane-2-thione

Conditions

Conditions	Yield
With potassium hydroxide In methanol for 96h; Ambient temperature;	82%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 123-51-3
i-Amyl alcohol

: 93314-60-4
11-ethyl-2-methyl-5,9-dioxa-7-pentadecanol

Conditions

Conditions	Yield
With sodium hydride for 48h; Ambient temperature;	79%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 2915-23-3
4-(4,6-diphenyl-pyrimidin-2-yl)-benzene-1,3-diol

: 163263-83-0
C33H38N2O4

Conditions

Conditions	Yield
With ethyltriphenylphosphonium bromide at 150℃; for 0.5h;	71.7%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 137-32-6
(+/-)-2-methyl-1-butanol

: 174719-45-0
11-ethyl-3-methyl-5,9-dioxa-7-pentadecanol

Conditions

Conditions	Yield
With sodium hydride for 48h; Ambient temperature;	69%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: C9H9N*HO3S

: sulfuric acid mono-[2-(3,4-dihydro-isoquinolin-2-yl)-1-(2-ethyl-hexyloxymethy)-ethyl] ester

Conditions

Conditions	Yield
at 75 - 80℃; for 72h; Product distribution / selectivity;	68%

: 230-27-3
7,8-benzoquinoline

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 1-(benzo[h]quinolin-10-yl)-3-((2-ethylhexyl)oxy)-2-propanol

Conditions

Conditions	Yield
With 1,1,1,3',3',3'-hexafluoro-propanol; palladium diacetate; acetic acid at 25℃; for 24h; Inert atmosphere;	58%

: 3230-65-7
3,4-dihydroisoquinoline

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: sulfuric acid mono-[2-(3,4-dihydro-isoquinolin-2-yl)-1-(2-ethyl-hexyloxymethy)-ethyl] ester

Conditions

Conditions	Yield
In acetonitrile at 80℃; for 72h; Product distribution / selectivity;	55%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 3,4,9,10-perylenetetracarboxylic diimide bis(tetrabutylammonium) salt

: C46H54N2O8

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 100℃; for 10h; Inert atmosphere;	50%

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 9-ethyl-5-(5-methyl-2-oxa-1-hexyl)-4,7-dioxa-1-tridecanesulfonic acid sodium salt

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 98 percent / sodium hydride / dimethylformamide / 3 h View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 12-ethyl-8-(5-methyl-2-oxa-1-hexyl)-4,7,10-trioxa-1-hexadecanesulfonic acid sodium salt

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: sodium hydride / acetonitrile / 0.5 h / Heating; before reflux 1 h room temperature 3: 1M HCl / 2 h / Heating 4: 100 percent / sodium hydride / dimethylformamide / 1 h / 60 °C View Scheme
Multi-step reaction with 4 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature 4: 100 percent / sodium hydride / dimethylformamide / 1 h / 60 °C View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-33-6
6-ethyl-4-oxadecane-1,2-dithiol

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 97.4 percent / thiourea / methanol / 48 h / Ambient temperature 2: 37 percent / sodium hydrosulfide, hydrogen sulfide / ethanol / 3 h View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-47-2
8-ethyl-4-(4-methyl-2-oxa-1-hexyl)-3,6-dioxa-1-dodecanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 69 percent / sodium hydride / 48 h / Ambient temperature 2: 93 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-42-7
8-ethyl-4-(5-methyl-2-oxa-1-hexyl)-3,6-dioxa-1-dodecanol

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: sodium hydride / acetonitrile / 0.5 h / Heating; before reflux 1 h room temperature 3: 1M HCl / 2 h / Heating View Scheme
Multi-step reaction with 3 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 11-ethyl-2-methyl-5,9-dioxa-7-pentadecanone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: PDC / dimethylformamide View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 11-ethyl-3-methyl-5,9-dioxa-7-pentadecanone

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 69 percent / sodium hydride / 48 h / Ambient temperature 2: PDC / dimethylformamide View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-44-9
11-ethyl-7-(5-methyl-2-oxa-1-hexyl)-3,6,9-trioxa-1-pentadecanol

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: sodium hydride / acetonitrile / 0.5 h / Heating; before reflux 1 h room temperature 3: 1M HCl / 2 h / Heating 4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature View Scheme
Multi-step reaction with 5 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature 4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature View Scheme

Yield

Multi-step reaction with 5 steps
1: 79 percent / sodium hydride / 48 h / Ambient temperature
2: sodium hydride / acetonitrile / 0.5 h / Heating; before reflux 1 h room temperature
3: 1M HCl / 2 h / Heating
4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C
5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature
View Scheme

Multi-step reaction with 5 steps
1: 79 percent / sodium hydride / 48 h / Ambient temperature
2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C
3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature
4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C
5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature
View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-49-4
11-ethyl-7-(4-methyl-2-oxa-1-hexyl)-3,6,9-trioxa-1-pentadecanol

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 69 percent / sodium hydride / 48 h / Ambient temperature 2: 93 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature 4: 17 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature View Scheme

Yield

Multi-step reaction with 5 steps
1: 69 percent / sodium hydride / 48 h / Ambient temperature
2: 93 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C
3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature
4: 17 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C
5: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature
View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-46-1
9-ethyl-5-(4-methyl-2-oxa-1-hexyl)-4,7-dioxa-1-tridecene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 69 percent / sodium hydride / 48 h / Ambient temperature 2: 93 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-41-6
9-ethyl-5-(5-methyl-2-oxa-1-hexyl)-4,7-dioxa-1-tridecene

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-43-8
12-ethyl-8-(5-methyl-2-oxa-1-hexyl)-4,7,10-trioxa-1-hexadecene

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: sodium hydride / acetonitrile / 0.5 h / Heating; before reflux 1 h room temperature 3: 1M HCl / 2 h / Heating 4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C View Scheme
Multi-step reaction with 4 steps 1: 79 percent / sodium hydride / 48 h / Ambient temperature 2: 89 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature 4: 78.7 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C View Scheme

: 2461-15-6
2-ethyl-hexyl glycidyl ether

: 174719-48-3
12-ethyl-8-(4-methyl-2-oxa-1-hexyl)-4,7,10-trioxa-1-hexadecene

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 69 percent / sodium hydride / 48 h / Ambient temperature 2: 93 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C 3: 1.) ozone, 2.) sodium borohydride / 1.) methanol, -78 deg C, 2.) methanol, to room temperature 4: 17 percent / sodium hydride / tetrahydrofuran / 22 h / 60 °C View Scheme

2-Ethylhexyl glycidyl ether Consensus Reports

Reported in EPA TSCA Inventory.

2-Ethylhexyl glycidyl ether Specification

The 2-Ethylhexyl glycidyl ether, with the CAS registry number 2461-15-6, is also known as Oxirane,2-[[(2-ethylhexyl)oxy]methyl]-. It belongs to the product categories of Oxiranes; Simple 3-Membered Ring Compounds; Epoxide Monomers; Monomers; Polymer Science. Its EINECS number is 219-553-6. This chemical's molecular formula is C₁₁H₂₂O₂ and molecular weight is 186.29. What's more, its systematic name is 2-{[(2-Ethylhexyl)oxy]methyl}oxirane. Its classification codes are: (1)Mutation data; (2)TSCA Flag T [Subject to the Section 4 test rule under TSCA]. This chemical should be sealed and stored in a cool, ventilated and dry place. Moreover, it should be protected from light. It is used as active diluents to reduce resin viscosity and improve the flexibility. It is also used to pour electric products in filament winding so as to increase mechanical properties.

Physical properties of 2-Ethylhexyl glycidyl ether are: (1)ACD/LogP: 3.259; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 3.26; (4)ACD/LogD (pH 7.4): 3.26; (5)ACD/BCF (pH 5.5): 176.62; (6)ACD/BCF (pH 7.4): 176.62; (7)ACD/KOC (pH 5.5): 1412.64; (8)ACD/KOC (pH 7.4): 1412.64; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 8; (12)Polar Surface Area: 21.76 Å²; (13)Index of Refraction: 1.445; (14)Molar Refractivity: 54.289 cm³; (15)Molar Volume: 204.141 cm³; (16)Polarizability: 21.522×10^-24cm³; (17)Surface Tension: 31.69 dyne/cm; (18)Density: 0.913 g/cm³; (19)Flash Point: 96.667 °C; (20)Enthalpy of Vaporization: 47.703 kJ/mol; (21)Boiling Point: 259.452 °C at 760 mmHg; (22)Vapour Pressure: 0.021 mmHg at 25°C.

Uses of 2-Ethylhexyl glycidyl ether: it can be used to produce 2-(4-ethyl-2-oxaoctyl)thiirane at the ambient temperature. It will need reagent thiourea and solvent methanol with the reaction time of 48 hours. The yield is about 97.4%.

2-Ethylhexyl glycidyl ether can be used to produce 2-(4-ethyl-2-oxaoctyl)thiirane at the ambient temperature

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need wear suitable protective clothing and eye/face protection.

You can still convert the following datas into molecular structure:
(1)SMILES: O(CC(CCCC)CC)CC1OC1
(2)Std. InChI: InChI=1S/C11H22O2/c1-3-5-6-10(4-2)7-12-8-11-9-13-11/h10-11H,3-9H2,1-2H3
(3)Std. InChIKey: BBBUAWSVILPJLL-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
rat	LD50	oral	7800mg/kg (7800mg/kg)		"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2A, Pg. 2210, 1981.

Product Name

2-Ethylhexyl glycidyl ether

Synthetic route

2-Ethylhexyl glycidyl ether Consensus Reports

2-Ethylhexyl glycidyl ether Specification

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