Cas no 10287-53-3 (Ethyl 4-dimethylaminobenzoate)

Ethyl 4-dimethylaminobenzoate, a derivative of benzoic acid, offers unique chemical properties. Its amine group enhances solubility in organic solvents, making it suitable for various applications. Its aromatic structure contributes to its stability and resistance to degradation, making it a valuable compound in pharmaceuticals and fragrances.
Ethyl 4-dimethylaminobenzoate structure
Ethyl 4-dimethylaminobenzoate structure
Product Name:Ethyl 4-dimethylaminobenzoate
CAS No:10287-53-3
MF:C11H15NO2
MW:193.242303133011
MDL:MFCD00009115
CID:48494
Update Time:2026-05-14

Ethyl 4-dimethylaminobenzoate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 4-dimethylaminobenzoate
    • 4-Dimethylaminobenzoic acid ethyl ester
    • EDB
    • Ethyl-4-(dimethylamino)benzoate
    • Ethyl-4-dimethylamino benzoate
    • Photoinitiator-EPD
    • Ethyl 4-(Dimethylamino)benzoate
    • Ethyl p-Dimethylaminobenzoate
    • Ethyl-P-Dimethylaminobenzoate
    • 4-(Dimethylamino)benzoic Acid Ethyl Ester
    • Parbenate
    • Ethyl p-N,N-dimethylaminobenzoate
    • YF-PI EDB
    • IHT-PI EDB
    • HRcure-EDB
    • SYNCURE EPD
    • Darocur EDB
    • OMNIRAD EDB
    • Darocure EDB
    • SPEEDCURE EDB
    • 4-dimethylamino-benzoic acid ethyl ester
    • Benzoic acid, 4-(dimethylamino)-, ethyl ester
    • Kayacure EPA
    • Ethyl-4-dimethylaminobenzoate
    • N,N-Dimethylbenzocaine
    • 829S8D3Y0X
    • Genocure EPD
    • Darocur EBD
    • Quantacure epd
    • PubChem20906
    • Maybridge3_003189
    • Benzoic
    • MDL: MFCD00009115
    • Inchi: 1S/C11H15NO2/c1-4-14-11(13)9-5-7-10(8-6-9)12(2)3/h5-8H,4H2,1-3H3
    • InChI Key: FZUGPQWGEGAKET-UHFFFAOYSA-N
    • SMILES: O(C([H])([H])C([H])([H])[H])C(C1C([H])=C([H])C(=C([H])C=1[H])N(C([H])([H])[H])C([H])([H])[H])=O
    • BRN: 2210233

Computed Properties

  • Exact Mass: 193.11000
  • Monoisotopic Mass: 193.11
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 184
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 2.9
  • Topological Polar Surface Area: 29.5

Experimental Properties

  • Color/Form: White crystalline powder
  • Density: 1.061
  • Melting Point: 63-66?°C (lit.)
  • Boiling Point: 190-191°C 14mm
  • Flash Point: 190-191°C/14mm
  • Refractive Index: 1.5080 (estimate)
  • Water Partition Coefficient: Insoluble
  • Stability/Shelf Life: Stable. Incompatible with reducing agents, oxidizing agents, bases, acids.
  • PSA: 29.54000
  • LogP: 1.92930
  • Solubility: Insoluble in water.

Ethyl 4-dimethylaminobenzoate Security Information

  • Signal Word:Warning
  • Hazard Statement: H303,H313
  • Warning Statement: P312
  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3
  • Hazard Category Code: R36/37/38
  • Safety Instruction: S37/39-S26
  • Hazardous Material Identification: Xi
  • TSCA:Yes
  • Storage Condition:Store at room temperature
  • Risk Phrases:R36/37/38
  • Safety Term:S26;S37/39

Ethyl 4-dimethylaminobenzoate Customs Data

  • HS CODE:29224995
  • Customs Data:

    China Customs Code:

    2922499990

    Overview:

    2922499990 Other amino acids and their esters and their salts(Except those containing more than one oxygen-containing group). VAT:17.0% Tax refund rate:9.0% Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods) MFN tariff:6.5% general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Regulatory conditions:

    A.Customs clearance form for Inbound Goods
    B.Customs clearance form for outbound goods

    Inspection and quarantine category:

    P.Imported animals and plants\Quarantine of animal and plant products
    Q.Outbound animals and plants\Quarantine of animal and plant products
    R.Sanitary supervision and inspection of imported food
    S.Sanitary supervision and inspection of exported food
    M.Import commodity inspection
    N.Export commodity inspection

    Summary:

    HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

Ethyl 4-dimethylaminobenzoate Pricemore >>

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Ethyl 4-dimethylaminobenzoate Production Method

Production Method 1

Reaction Conditions
1.1R:NaBH3CN, S:AcOH, overnight, rt
1.2R:NaOH, S:H2O, 30 min, 0°C
Reference
Synthesis of Phenols from Aryl Ammonium Salts under Mild Conditions
By Ni, Pufan et al, Journal of Organic Chemistry, 2022, 87(19), 12677-12687

Production Method 2

Reaction Conditions
1.1R:t-BuOK, C:RuCl3, S:MeOH, 36 h, 150°C
Reference
Simple RuCl3-catalyzed N-Methylation of Amines and Transfer Hydrogenation of Nitroarenes using Methanol
By Sarki, Naina et al, ChemCatChem, 2021, 13(7), 1722-1729

Production Method 3

Reaction Conditions
1.1R:HCO2Me, R:AcONa, S:MeOH, S:H2O, 24 h, 160°C
Reference
Alkyl formates as reagents for reductive amination of carbonyl compounds
By Afanasyev, Oleg I. et al, Mendeleev Communications, 2020, 30(1), 112-113

Production Method 4

Reaction Conditions
1.1R:Et3N, S:DMSO, 12-48 h, 150°C; 150°C → rt
1.2R:NaOH, S:H2O, rt, basify
Reference
Highly Efficient Binuclear Copper-catalyzed Oxidation of N,N-Dimethylanilines with O2
By Liu, Yuxia et al, ChemCatChem, 2020, 12(8), 2221-2225

Production Method 5

Reaction Conditions
1.1R:H2, C:PtO2, rt → 60°C; 40 h, 60°C, 0.1-0.2 MPa
Reference
Facile, highly efficient and environmentally friendly transesterification mediated by platinum dioxide and nickel oxide under essentially neutral conditions
By Teng, Binhao et al, Green Chemistry, 2018, 20(11), 2465-2471

Production Method 6

Reaction Conditions
1.1R:Mn, C:CoBr2, C:Me3SiCl, C:2,2'-(C5H4N)2, S:DMF, S:C5H5N, 20 h, 60°C
Reference
Cobalt-Catalyzed Esterification of Amides
By Bourne-Branchu, Yann et al, Chemistry - A European Journal, 2017, 23(42), 10043-10047

Production Method 7

Reaction Conditions
1.1R:4-DMAP, C:PdCl2(PPh3)2, S:EtOH, 20 min, 140°C, 5-7 bar
Reference
Diethyl oxalate as "CO" source for palladium-catalyzed ethoxycarbonylation of bromo- and chloroarene derivatives
By Monrose, Amandine et al, Advanced Synthesis & Catalysis, 2017, 359(15), 2699-2704

Production Method 8

Reaction Conditions
1.1R:(Me2N)3P=O, C:22784-59-4, S:PhMe, 100°C
Reference
Ethyl chloroformate
By Payne, Andrew N. and Kobayashi, Yuichi, e-EROS Encyclopedia of Reagents for Organic Synthesis, 2005, From e-EROS Encyclopedia of Reagents for Organic Synthesis, 1-6

Production Method 9

Reaction Conditions
1.1R:Ph2SiH2, C:107-43-7, S:MeCN, rt; 12 h, 70°C, 1 bar
Reference
Betaine Catalysis for Hierarchical Reduction of CO2 with Amines and Hydrosilane To Form Formamides, Aminals, and Methylamines
By Liu, Xiao-Fang et al, Angewandte Chemie, 2017, 56(26), 7425-7429

Production Method 10

Reaction Conditions
1.1R:H2, C:Co(OAc)2, C:23582-02-7, C:Sn(O3SCF3)2, S:EtOH, 24 h, 125°C, 9 MPa
Reference
Alcohol promoted N-methylation of anilines with CO2/H2 over a cobalt catalyst under mild conditions
By Ke, Zhengang et al, Green Chemistry, 2021, 23(22), 9147-9153

Production Method 11

Reaction Conditions
1.1R:H2SO4, 2 h, 72°C
Reference
Design, synthesis, in vitro and in vivo evaluation against MRSA and molecular docking studies of novel pleuromutilin derivatives bearing 1, 3, 4-oxadiazole linker
By Liu, Jie et al, Bioorganic Chemistry, 2021, 112, 104956

Production Method 12

Reaction Conditions
1.1R:PhSiH3, S:MeCN, 10 min, rt
Reference
Metal-Free Deoxygenation of Amine N-Oxides: Synthetic and Mechanistic Studies
By Lecroq, William et al, ChemPhysChem, 2021, 22(12), 1237-1242

Production Method 13

Reaction Conditions
1.1R:Et3N, S:MeCN, 5 min, rt
1.2rt; overnight, rt
2.1R:LiCl, S:H2O, rt
2.2R:AcOH, 30 min, rt
2.330 min, rt; rt → 0°C
2.4R:NaNO2, S:H2O, 0°C; 1 h, 0°C; 0°C → rt; 5 h, rt
3.1R:Disodium carbonate, S:H2O, S:Dioxane, 2 h, 60°C
3.24 h, 60°C
Reference
Imidazotetrazines as Weighable Diazomethane Surrogates for Esterifications and Cyclopropanations
By Svec, Riley L. and Hergenrother, Paul J., Angewandte Chemie, 2020, 59(5), 1857-1862

Production Method 14

Reaction Conditions
1.1R:H2SO4, R:NaBH4, S:H2O, S:THF, 0°C
1.2R:H2SO4, S:H2O, 0°C, acidify
1.3R:H2SO4, S:H2O, S:THF, 0°C
1.4S:H2O, 0°C
1.5R:KOH, 0°C, pH 10
Reference
Reductive Coupling between C-N and C-O Electrophiles
By He, Rong-De et al, Journal of the American Chemical Society, 2019, 141(32), 12481-12486

Production Method 15

Reaction Conditions
1.1R:PhSiH3, S:DMF, 4 h, 80°C, 1 bar
Reference
DMF-promoted reductive functionalization of CO2 with secondary amines and phenylsilane to methylamines
By Liu, Xiao-Fang et al, Pure and Applied Chemistry, 2018, 90(7), 1099-1107

Production Method 16

Reaction Conditions
1.1R:Ph2SiH2, C:2254080-71-0, S:MeCN, 24 h, 120°C, 2.7 atm
Reference
Diverse catalytic reactivity of a dearomatized PN3P*-nickel hydride pincer complex towards CO2 reduction
By Li, Huaifeng et al, Chemical Communications (Cambridge, 2018, 54(81), 11395-11398

Production Method 17

Reaction Conditions
1.1R:NaH, S:THF, 0°C; 10 min, 0°C; 45 min, rt
1.2overnight, rt
1.3R:H2O, 0°C
2.1C:54761-04-5, S:MeCN, 48 h, 90°C
Reference
Broadly Applicable Ytterbium-Catalyzed Esterification, Hydrolysis, and Amidation of Imides
By Guissart, Celine et al, Organic Letters, 2018, 20(17), 5098-5102

Production Method 18

Reaction Conditions
1.1R:O2, C:752-13-6, C:HCl, S:EtOH, S:MeCN, 12 h, cooled
Reference
Visible-Light-Driven Aerobic Photooxidation of Aldehydes to Methyl Esters Catalyzed by Riboflavin Tetraacetate
By Muehldorf, Bernd and Wolf, Robert, ChemCatChem, 2017, 9(6), 920-923

Production Method 19

Reaction Conditions
1.1R:PhSiH3, S:DMF, 24 h, 90°C, 1 atm; 90°C → rt
1.2R:H2O, rt
Reference
Catalyst-free N-methylation of amines using CO2
By Niu, Huiying et al, Chemical Communications (Cambridge, 2017, 53(6), 1148-1151

Production Method 20

Reaction Conditions
1.1R:CaH2, C:Pd, S:5614-37-9, 16 h, 80°C
Reference
Reductive N-methylation of amines with calcium hydride and Pd/C catalyst
By Guyon, Carole et al, Tetrahedron Letters, 2016, 57(27-28), 3002-3005

Ethyl 4-dimethylaminobenzoate Raw materials

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Tiancheng Chemical (Jiangsu) Co., Ltd
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Quantity:25KG,200KG,1000KG
Purity:99%
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(CAS:10287-53-3)Ethyl 4-dimethylaminobenzoate
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Purity:99.9%
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Tiancheng Chemical (Jiangsu) Co., Ltd
(CAS:10287-53-3)Ethyl 4-dimethylaminobenzoate
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Quantity:25KG,200KG,1000KG/25KG,200KG,1000KG/25KG,200KG,1000KG
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Suzhou Senfeida Chemical Co., Ltd
(CAS:10287-53-3)Ethyl 4-dimethylaminobenzoate
sfd16519
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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