Phenethyl Phenylacetate supplier

Name
Phenethyl phenylacetate
EINECS 203-013-1
CAS No. 102-20-5
Article Data50
CAS DataBase
Density 1.082 g/cm³
Solubility 15.56-22mg/L at 20-22℃
Melting Point 28 °C(lit.)
Formula C₁₆H₁₆O₂
Boiling Point 359.9 °C at 760 mmHg
Molecular Weight 240.302
Flash Point 145.8 °C
Transport Information
Appearance
Safety 26-36
Risk Codes 36/38
Molecular Structure
Hazard Symbols Xi
Synonyms Benzylcarbinyl a-toluate;NSC 6676;Phenethyl phenylacetate;Phenylethyl phenylacetate;b-Phenylethyl phenylacetate;Aceticacid, phenyl-, phenethyl ester (6CI,7CI,8CI);2-Phenylethyl phenylacetate;
PSA 26.30000
LogP 3.01500

Synthetic route

: 60-12-8
2-phenylethanol

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 122-78-1
phenylacetaldehyde

Conditions

Conditions	Yield
With silica gel; 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium perchlorate In dichloromethane	A 4% B 99%
With pyridine; 4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl; iodine; sodium hydrogencarbonate In dichloromethane; water at 20 - 25℃; for 3h;	A 58.7% B 41.3%
With oxygen at 120℃; for 5h; Neat (no solvent);
With pyridine; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; iodine; sodium hydrogencarbonate In dichloromethane; water at 20 - 22℃; for 3h; Catalytic behavior; Time;	A 71 %Chromat. B 23 %Chromat.
With 2,6-dimethylpyridine; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; iodine; sodium hydrogencarbonate In dichloromethane; water at 20 - 22℃; for 3h; Catalytic behavior; Time;	A 12 %Chromat. B 86 %Chromat.

: 103-82-2
phenylacetic acid

: 60-12-8
2-phenylethanol

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With potassium hydroxide	98.6%
With C10H10Zr(2+)2CF3O3S(1-)C4H8O at 80℃; for 24h; Sealed tube;	95%
With silica gel-immobilized perchloric acid at 80℃; for 6h; Fischer esterification; Inert atmosphere; Neat (no solvent);	94%

: 60-12-8
2-phenylethanol

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With periodic acid; pyridinium chlorochromate In acetonitrile at 0 - 20℃; for 2h;	94%
With sodium bromite In water; acetic acid for 10h; Ambient temperature;	91%
With peracetic acid; sodium bromide In ethyl acetate at 39.9℃; for 2h;	86%

: 60-12-8
2-phenylethanol

: 75-64-9
tert-butylamine

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 24070-10-8
2-methyl-N-phenethylpropan-2-amine

Conditions

Conditions	Yield
With 3 A molecular sieve; potassium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; [Ru(p-cumene)Cl2]2 In toluene at 110℃; for 24h; Product distribution; Further Variations:; Catalysts;	A 7% B 88%
With 3 A molecular sieve; potassium carbonate; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; [Ru(p-cumene)Cl2]2 In toluene at 110℃; for 24h;	A 61% B n/a

...Expand

: 122-78-1
phenylacetaldehyde

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With Rh(PhBP3)(H)2(NCMe); hydrogen In toluene at 20℃; under 760.051 Torr; for 0.166667h; Tishchenko reaction;	85%

: 60-12-8
2-phenylethanol

: 536-74-3
phenylacetylene

A: 103-82-2
phenylacetic acid

B: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With dihydrogen peroxide; methyltrioxorhenium(VII) for 48h;	A 50% B 47%

...Expand

: 60-12-8
2-phenylethanol

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 108-88-3
toluene

Conditions

Conditions	Yield
With [RuCl2(p-cymene)(iPr2-imy)]; potassium hydroxide; tricyclohexylphosphine In 1,3,5-trimethyl-benzene at 163℃; for 18h; Inert atmosphere;	A 48% B 7%

: 60-12-8
2-phenylethanol

: 142-84-7
di-n-propylamine

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 25173-09-5
2-phenyl-N,N-dipropylacetamide

Conditions

Conditions	Yield
With C15H22Cl2N2Ru; potassium tert-butylate In toluene for 24h; Inert atmosphere; Reflux;	A 21% B 44%

...Expand

: 60-12-8
2-phenylethanol

: 103-49-1
dibenzylamine

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 102459-18-7
N,N-dibenzyl-2-phenylacetamide

Conditions

Conditions	Yield
With C15H22Cl2N2Ru; potassium tert-butylate In toluene for 24h; Inert atmosphere; Reflux;	A 19% B 40%

...Expand

: 103-82-2
phenylacetic acid

A: 60-12-8
2-phenylethanol

B: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With rhenium-catalyst at 149℃; under 117681 Torr; Hydrogenation;
With tin(II) trifluoromethanesulfonate; tris(2,4-pentanedionato)ruthenium(III); hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In water; toluene at 160℃; under 45004.5 Torr; for 48h; Reagent/catalyst; Autoclave;	A 49 %Chromat. B 20 %Chromat.

: 103-82-2
phenylacetic acid

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With sulfuric acid bei der elektrolytischen Reduktion an einer Bleikathode;
With tin(II) trifluoromethanesulfonate; tris(2,4-pentanedionato)ruthenium(III); hydrogen; [2-((diphenylphospino)methyl)-2-methyl-1,3-propanediyl]bis[diphenylphosphine] In toluene at 160℃; under 45004.5 Torr; for 48h; Reagent/catalyst; Autoclave;	26 %Chromat.

: 555-75-9
aluminum ethoxide

: 122-78-1
phenylacetaldehyde

: 102-20-5
phenyl-acetic acid phenethyl ester

: 103-80-0
phenylacetyl chloride

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With triphenylstannane

: 101-97-3
Ethyl 2-phenylethanoate

A: 5421-17-0
Phenylessigsaeurehexylester

B: 102-20-5
phenyl-acetic acid phenethyl ester

C: 122-45-2
phenylacetic acid octyl ester

Conditions

Conditions	Yield
Product distribution; competition reaction with n-hexanol, n-octanol and phenylethanol; selectivity of catalysis with SiO2, also mod. with Ph-CH<(EtO)3SiO>-P(O)(OEt)(OHex) or H2SO4;

...Expand

: 60-29-7
diethyl ether

: 103-80-0
phenylacetyl chloride

: 71-43-2
benzene

magnesium: magnesium

magnesium iodide: magnesium iodide

A: 102-20-5
phenyl-acetic acid phenethyl ester

B acid C18H18O3 of mp: 198 degree: acid C18H18O3 of mp: 198 degree

...Expand

: 103-82-2
phenylacetic acid

: 7664-93-9
sulfuric acid

: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
at 70℃; bei der Elektrolyse an einer Bleikathode.Diazotization;

: 103-82-2
phenylacetic acid

rhenium: rhenium

A: 60-12-8
2-phenylethanol

B: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
at 150℃; under 117681 Torr; Hydrogenation;

...Expand

: 60-12-8
2-phenylethanol

: 7664-93-9
sulfuric acid

dichromate: dichromate

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 100-52-7
benzaldehyde

C: 64-19-7
acetic acid

D: 65-85-0
benzoic acid

...Expand

: 60-12-8
2-phenylethanol

: 100-51-6
benzyl alcohol

A: 102-16-9
benzyl 2-phenylacetate

B: 120-51-4
benzoic acid benzyl ester

C: 94-47-3
2-Phenylethyl benzoate

D: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With magnesium nitride; [RuCl2(p-cymene)(iPr2-imy)]; potassium tert-butylate; tricyclohexylphosphine tetrafluoroborate In toluene at 110℃; for 24h; Schlenk technique; Inert atmosphere;

...Expand

: 98-85-1, 13323-81-4
1-Phenylethanol

: 60-12-8
2-phenylethanol

A: 102-20-5
phenyl-acetic acid phenethyl ester

B: 98-86-2
acetophenone

Conditions

Conditions	Yield
With magnesium nitride; [RuCl2(p-cymene)(iPr2-imy)]; potassium tert-butylate; tricyclohexylphosphine tetrafluoroborate In toluene at 110℃; for 24h; Schlenk technique; Inert atmosphere;

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 60-12-8
2-phenylethanol

: 555-16-8
4-nitrobenzaldehdye

: 123-11-5
4-methoxy-benzaldehyde

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

A: 530-48-3
1,1-Diphenylethylene

B: 5455-87-8
4-methoxy-N-(4-nitrobenzylidene)aniline

C: 6290-08-0
p-methoxybenzaldehyde neopentyl glycol acetal

D: 102-20-5
phenyl-acetic acid phenethyl ester

E: 1749-08-2
N-(4-methoxy benzylidene)-4-methoxyaniline

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 75 %Spectr. C 72 %Spectr. D 59 %Spectr. E 5 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 60-12-8
2-phenylethanol

: 104-88-1
4-chlorobenzaldehyde

: 555-16-8
4-nitrobenzaldehdye

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

A: 530-48-3
1,1-Diphenylethylene

B: 5455-87-8
4-methoxy-N-(4-nitrobenzylidene)aniline

C: 6283-10-9
2-(4-chlorophenyl)-5,5-dimethyl-1,3-dioxane

D: 838-42-6
5,5-dimethyl-2-(4-nitro-phenyl)-[1,3]dioxane

E: 1749-03-7
N-(4-chlorobenzylidene)-4-methoxyaniline

F: 102-20-5
phenyl-acetic acid phenethyl ester

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 52 %Spectr. C 52 %Spectr. D 48 %Spectr. E 43 %Spectr. F 99 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 106-47-8
4-chloro-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

: 613-45-6
2,4-Dimethoxybenzaldehyde

A: 530-48-3
1,1-Diphenylethylene

B: 102-20-5
phenyl-acetic acid phenethyl ester

C: 1620217-69-7
2-(2,4-dimethoxyphenyl)-5,5-dimethyl-1,3-dioxane

D: 354538-08-2
4-chloro-N-(2,4-dinitrobenzylidene)aniline

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 99 %Spectr. C 74 %Spectr. D 83 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

: 98-80-6
phenylboronic acid

A: 530-48-3
1,1-Diphenylethylene

B: 354538-06-0
N-(2,4-dinitrobenzylidene)-4-methoxyaniline

C: 102-20-5
phenyl-acetic acid phenethyl ester

D: 5123-13-7
5,5-dimethyl-2-phenyl-1,3,2-dioxaborinane

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 98 %Spectr. B 93 %Spectr. C 99 %Spectr. D 99 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 1582-24-7
pentafluorophenylboronic acid

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

A: 530-48-3
1,1-Diphenylethylene

B: 354538-06-0
N-(2,4-dinitrobenzylidene)-4-methoxyaniline

C: 102-20-5
phenyl-acetic acid phenethyl ester

D: 1262967-46-3
(2,3,4,5,6-pentafluorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 97 %Spectr. C 99 %Spectr. D 74 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

: 613-45-6
2,4-Dimethoxybenzaldehyde

A: 530-48-3
1,1-Diphenylethylene

B: 354538-06-0
N-(2,4-dinitrobenzylidene)-4-methoxyaniline

C: 102-20-5
phenyl-acetic acid phenethyl ester

D: 1620217-69-7
2-(2,4-dimethoxyphenyl)-5,5-dimethyl-1,3-dioxane

E: 123794-61-6
N-(2,4-dimethoxybenzylidene)-4-methoxyaniline

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 84 %Spectr. C 96 %Spectr. D 77 %Spectr. E 9 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 126-30-7
2,2-Dimethyl-1,3-propanediol

: 62-53-3
aniline

: 613-45-6
2,4-Dimethoxybenzaldehyde

A: 530-48-3
1,1-Diphenylethylene

B: 102-20-5
phenyl-acetic acid phenethyl ester

C: 1620217-69-7
2-(2,4-dimethoxyphenyl)-5,5-dimethyl-1,3-dioxane

D: 149742-71-2, 97946-02-6
1-(2,4-dinitrophenyl)-N-phenylmethanimine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 98 %Spectr. C 80 %Spectr. D 86 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 108-91-8
cyclohexylamine

: 126-30-7
2,2-Dimethyl-1,3-propanediol

: 613-45-6
2,4-Dimethoxybenzaldehyde

A: 530-48-3
1,1-Diphenylethylene

B: 102-20-5
phenyl-acetic acid phenethyl ester

C: 1620217-69-7
2-(2,4-dimethoxyphenyl)-5,5-dimethyl-1,3-dioxane

D: 553662-91-2
N-(2,4-dinitrobenzylidene)cyclohexanamine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 43 %Spectr. C 95 %Spectr. D 72 %Spectr.

...Expand

: 103-82-2
phenylacetic acid

: 599-67-7
1,1-diphenylethanol

: 528-75-6
2,4-dinitrobenzaldehyde

: 60-12-8
2-phenylethanol

: 100-52-7
benzaldehyde

: 104-94-9
4-methoxy-aniline

: 126-30-7
2,2-Dimethyl-1,3-propanediol

A: 530-48-3
1,1-Diphenylethylene

B: 776-88-5
5,5-dimethyl-2-phenyl-[1,3]dioxane

C: 354538-06-0
N-(2,4-dinitrobenzylidene)-4-methoxyaniline

D: 102-20-5
phenyl-acetic acid phenethyl ester

E: 783-08-4
[4-(benzylideneamino)phenyl]methanol

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In toluene for 48h; Inert atmosphere; Reflux; Dean-Stark;	A 99 %Spectr. B 79 %Spectr. C 92 %Spectr. D 98 %Spectr. E 5 %Spectr.

...Expand

: 67-56-1
methanol

: 102-20-5
phenyl-acetic acid phenethyl ester

: 101-41-7
benzeneacetic acid methyl ester

Conditions

Conditions	Yield
With 1-butyl-3-methylimidazolium tetrachloridoferrate(III) at 146.84℃; for 6h; Reagent/catalyst;	96.6%

: 102-20-5
phenyl-acetic acid phenethyl ester

: 2396-53-4
di(2-phenylethyl) ether

Conditions

Conditions	Yield
With triiron dodecarbonyl; 1,1,3,3-Tetramethyldisiloxane In toluene at 100℃; for 2h; Inert atmosphere; Schlenk technique;	85%

: 102-20-5
phenyl-acetic acid phenethyl ester

: 106-95-6
allyl bromide

: 1181399-18-7
phenethyl 2-phenylpent-4-enoate

Conditions

Conditions	Yield
With caesium hydroxide monohydrate; 2,7-bis[O(9)-allylhydrocinchonidinium-N-methyl]naphthalene dibromide In dichloromethane at -40℃; for 23h; Inert atmosphere; optical yield given as %ee; enantioselective reaction;	77%

: 102-20-5
phenyl-acetic acid phenethyl ester

: 244263-79-4
2-phenylethyl 2-oxo-2-phenylacetate

Conditions

Conditions	Yield
Stage #1: phenyl-acetic acid phenethyl ester With tert.-butylhydroperoxide; copper(II) oxide In water at 110℃; for 4.5h; Stage #2: With pyridine In water at 50℃; for 4h;	61%

: 102-20-5
phenyl-acetic acid phenethyl ester

: 292638-84-7
styrene

Conditions

Conditions	Yield
at 315 - 320℃;

: 102-20-5
phenyl-acetic acid phenethyl ester

A: 292638-84-7
styrene

B: 103-82-2
phenylacetic acid

Conditions

Conditions	Yield
at 315 - 320℃;

: 102-20-5
phenyl-acetic acid phenethyl ester

: 6921-34-2
benzylmagnesium chloride

: 6712-97-6
tribenzylcarbinol

Conditions

Conditions	Yield
With diethyl ether

: 102-20-5
phenyl-acetic acid phenethyl ester

: 96-09-3
styrene oxide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 315 - 320 °C 2: peroxybenzoic acid; chloroform / 0 °C View Scheme

: 102-20-5
phenyl-acetic acid phenethyl ester

: 880348-56-1
2-phenyl-acrylic Acid Phenethyl Ester

Conditions

Conditions	Yield
With tetra-(n-butyl)ammonium iodide; potassium carbonate; paraformaldehyde In diethyl ether; toluene	1.48 g (60%)

: 102-20-5
phenyl-acetic acid phenethyl ester

: 106-95-6
allyl bromide

: 1181399-16-5
(+/-)-phenethyl 2-phenylpent-4-enoate

Conditions

Conditions	Yield
With caesium hydroxide monohydrate; tetrabutylammomium bromide In dichloromethane at 0 - 20℃; for 16h; Inert atmosphere;

: 102-20-5
phenyl-acetic acid phenethyl ester

: 60-12-8
2-phenylethanol

Conditions

Conditions	Yield
Stage #1: phenyl-acetic acid phenethyl ester With iron (II) stearate; ethylenediamine In toluene at 20℃; for 0.0833333h; Inert atmosphere; Schlenk technique; Stage #2: In toluene at 100℃; for 20h; Inert atmosphere; Schlenk technique;	84 %Chromat.
Stage #1: phenyl-acetic acid phenethyl ester With C33H58FeN3PSi2; phenylsilane In toluene at 20℃; for 4h; Inert atmosphere; Glovebox; Green chemistry; Stage #2: With sodium hydroxide In toluene for 1h; Green chemistry;

Phenethyl Phenylacetate Chemical Properties

Name: Phenethyl phenylacetate
Synonyms: FEMA 2866;BETA PHENYL ETHYL PHENYL ACETATE;B-PHENYLETHYL PHENYLACETATE;2-PHENYLETHYL PHENYLACETATE;PHENYL ETHYL PHENYL ACETATE;PHENYLACETIC ACID 2-PHENYLETHER ESTER;PHENYLACETIC ACID 2-PHENYLETHYL ESTER;PHENETHYL PHENYLACETATE
CAS: 102-20-5
Molecular Formula: C₁₆H₁₆O₂
Molecular Weight: 240.30
CAS Registry Number: 102-20-5
EINECS: 203-013-1
Density: 1.082
Melting point: 28 ^oC
Boiling point: 325 ^oC
Refractive index: 1.55
Flash point: 113 ^oC
FEMA: 2866
refractive index: n20/D 1.55(lit.)
Beilstein/Gmelin: 2214383
Beilstein Reference: 3-09-00-02183
Solubility in water: Insoluble
Vapor Pressure: 2.3E-5 (25 C)
Heat Of Vaporization: 60.6 kJ/mol

Phenethyl Phenylacetate Uses

Food additive

Phenethyl Phenylacetate Toxicity Data With Reference

RTECS AJ3255000

Phenethyl Phenylacetate Safety Profile

Hazard Codes: Xi
Risk Codes: R36/38
Safety Description: S26;S36
WGK Germany: 2
First Aid Measures
Ingestion
If swallowed, wash out mouth with water provided person is conscious and then call a physician.
Inhalation
If inhaled, remove to fresh air. If not breathing, give artificial respiration. If breathing is difficult, give oxygen.
Skin
In case of contact, wash skin with soap and plenty of water right away.
Eyes
In case of contact, flush eyes with plenty of water for 15 minutes or more.
Personal Protection
Wear protective gloves and goggles.

Phenethyl Phenylacetate Specification

This product should be kept tightly closed and stored in a cool dry place.

Small spills/leaks
Sweep up, place in a bag and hold for waste disposal. Avoid raising dust. Ventilate area and wash spill site after material pickup is complete.

Product Name

Phenethyl phenylacetate

Synthetic route

Phenethyl Phenylacetate Chemical Properties

Phenethyl Phenylacetate Uses

Phenethyl Phenylacetate Toxicity Data With Reference

Phenethyl Phenylacetate Safety Profile

Phenethyl Phenylacetate Specification

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