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Dibenzyl carbonate

CAS No.
3459-92-5
Chemical Name:
Dibenzyl carbonate
Synonyms
Benzyl carbonate;NSC 406789;Dibenzyl carbonate;dibenzyl carbazate;Dibenzylcarbonate,98%;Linezolid Impurity 50;Dibenzyl Carbonate >Dibenzyl carbonate 99%;carbonacidibenzyl ester;CARBONIC ACID DIBENZYL ESTER
CBNumber:
CB5677478
Molecular Formula:
C15H14O3
Molecular Weight:
242.27
MDL Number:
MFCD00014436
MOL File:
3459-92-5.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-09-12 18:53:38

Dibenzyl carbonate Properties

Melting point 29-33 °C(lit.)
Boiling point 180-190 °C2 mm Hg(lit.)
Density 1.1515 (rough estimate)
refractive index 1.5485
Flash point >230 °F
storage temp. Store at room temperature
solubility Sparingly Soluble (0.099 g/L) (25°C).
form powder to lump
color White to Almost white
Sensitive Air Sensitive
BRN 1882864
InChI 1S/C15H14O3/c16-15(17-11-13-7-3-1-4-8-13)18-12-14-9-5-2-6-10-14/h1-10H,11-12H2
InChIKey PIZLBWGMERQCOC-UHFFFAOYSA-N
SMILES O=C(OCc1ccccc1)OCc2ccccc2
CAS DataBase Reference 3459-92-5(CAS DataBase Reference)
FDA UNII 99TJK14RPZ
EPA Substance Registry System Carbonic acid, bis(phenylmethyl) ester (3459-92-5)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302+H312-H302-H312
Precautionary statements  P280-P264-P270-P301+P312+P330-P302+P352+P312+P362+P364-P501-P280h-P301+P312a-P321-P501a
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn
Risk Statements  21/22
Safety Statements  36
WGK Germany  3
TSCA  TSCA listed
HS Code  29209090
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
NFPA 704
1
2 0

Dibenzyl carbonate price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical C1600 Dibenzyl Carbonate >98.0%(GC) 3459-92-5 1g $41 2026-04-30 Buy
TCI Chemical C1600 Dibenzyl Carbonate >98.0%(GC) 3459-92-5 5g $163 2026-04-30 Buy
Usbiological 274640 Dibenzyl Carbonate Asreported 3459-92-5 5g $349 2026-06-03 Buy
Usbiological 274640 Dibenzyl Carbonate Asreported 3459-92-5 10g $490 2026-06-03 Buy
Usbiological 274640 Dibenzyl Carbonate Asreported 3459-92-5 25g $732 2026-06-03 Buy
Product number Packaging Price Buy
C1600 1g $41 Buy
C1600 5g $163 Buy
274640 5g $349 Buy
274640 10g $490 Buy
274640 25g $732 Buy

Dibenzyl carbonate Chemical Properties, Uses, Production

Chemical Properties

Colorless low melting solid

Uses

Ionic liquids can effectively accelerate slow N-benzylation reactions utilizing dibenzyl carbonate as an alkylating reagent. Dibenzyl carbonate (DBzlC) has been used to benzylate phenylacetonitrile, benzyl phenylacetate and phenol. Selective N, N-dibenzylation of primary aliphatic amines was carried with dibenzyl carbonate in the presence of phosphonium salts.

Preparation

To a stirred solution of benzyl alcohol (0.216 g, 2.00 mol), tributylphosphine (0.303 g, 1.50 mmol), and CyTMG (0.394 g, 2.00 mmol) in DMF (2.00 mL), CO2 was added at room temperature. After 15 min, tetrabromomethane (0.663 g, 2.00 mmol) was added, the reaction vessel was sealed, and the contents were stirred for 2 h. Thereafter, the reaction mixture was diluted with ethyl acetate, washed successively with 0.5 m aqueous HCl and saturated aq. NaHCO3 solution, and dried over Na2SO4. Diphenylmetha- nol was added to the organic solution as an internal standard and the yield of dibenzyl carbonate was determined from the relative integrals of a methylene peak of the carbonate and a methine peak of diphenylmethanol in the 1H NMR spectrum of the ethyl acetate solution. Dibenzyl carbonate, prepared by a larger scale reaction of CO2 with benzyl alcohol (1.08 g, 10.0 mmol), was isolated by column chromatography (cyclohexane/ethyl acetate, 50:1) in 67.3% yield (0.816 g).

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 6205, 1995 DOI: 10.1021/jo00124a044

General Description

Dibenzyl carbonate (DBC) is commonly used as a benzylating agent. Dimethyl carbonate and excess of benzyl alcohol undergoes transesterification in the presence of CsF/α-Al2O3 (cesium fluoride/aluminum oxide) to form DBC. The formation of N,N-dibenzyl derivatives by the reaction of primary aliphatic amines with DBC in the presence of phosphonium salts has been investigated.

Dibenzyl carbonate Preparation Products And Raw materials

Dibenzyl carbonate Suppliers

Global Suppliers ( 160)
Supplier Tel Email Country ProdList Advantage
Creasyn Finechem(Tianjin) Co., Ltd. 022-83946278 13820372920 sales@creasyn.com China 968 68
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Adamas Reagent, Ltd. 400-6009262 15618770481 yhx@titansci.com China 14098 59
Shanghai Hanhong Scientific Co.,Ltd. 021-54306202 13764082696 info@hanhongsci.com China 42917 64
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57
Syntechem Co.,Ltd info@syntechem.com China 12973 57

View Latest Price from Dibenzyl carbonate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DIBENZYL CARBONATE pictures 2025-06-27 DIBENZYL CARBONATE
3459-92-5
1KG 99% 500000kg Hebei Chuanghai Biotechnology Co., Ltd
DIBENZYL CARBONATE pictures 2025-06-20 DIBENZYL CARBONATE
3459-92-5
$40.00 1kg 0.99 10 tons Hebei Yanxi Chemical Co., Ltd.
DIBENZYL CARBONATE pictures 2020-01-13 DIBENZYL CARBONATE
3459-92-5
$1.00 1g 99.0% 100 kg Career Henan Chemical Co

Dibenzyl carbonate Spectrum

Benzyl carbonate Carbonic acid, bis(phenylmethyl) ester CARBONIC ACID DIBENZYL ESTER Dibenzylcarbonate,98% dibenzyl carbazate NSC 406789 Dibenzyl carbonate 99% Linezolid Impurity 50 Dibenzyl Carbonate > carbonacidibenzyl ester Dibenzyl carbonate 3459-92-5 3459-92-6 C6H5CH2O2CO Carbonates Carbonyl Compounds Building Blocks Protection & Derivatization Reagents (for Synthesis) Organic Building Blocks Protection & Derivatization Reagents (for Synthesis) Synthetic Organic Chemistry Carbonates Carbonyl Compounds Organic Building Blocks