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CAS

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30379-54-5

Benzyl Benzyloxyacetate, also known as Benzyl phenylacetate, is an organic compound derived from benzoic acid and benzyl alcohol. It is widely used in the fragrance and food industries due to its sweet, floral, and slightly fruity odor. As a synthetic scent ingredient, it serves as a fixative in perfumes and a flavoring agent in food products. However, it is essential to handle and store this chemical with care to avoid skin and eye irritation.

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  • 30379-54-5 Structure

  • Basic information

    1. Product Name: Benzyl Benzyloxyacetate
    2. Synonyms: Benzyl Benzyloxyacetate;2-(PhenylMethoxy)acetic Acid PhenylMethyl Ester;NSC 153413;Benzyl 2-(benzyloxy)acetate
    3. CAS NO:30379-54-5
    4. Molecular Formula: C16H16O3
    5. Molecular Weight: 256
    6. EINECS: N/A
    7. Product Categories: Aromatics;Miscellaneous Reagents
    8. Mol File: 30379-54-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 386.4°C at 760 mmHg
    3. Flash Point: 138.6°C
    4. Appearance: /
    5. Density: 1.135g/cm3
    6. Vapor Pressure: 3.54E-06mmHg at 25°C
    7. Refractive Index: 1.56
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Benzyl Benzyloxyacetate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benzyl Benzyloxyacetate(30379-54-5)
    12. EPA Substance Registry System: Benzyl Benzyloxyacetate(30379-54-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 30379-54-5(Hazardous Substances Data)

30379-54-5 Usage

Uses

Used in the Fragrance Industry:
Benzyl Benzyloxyacetate is used as a fixative in perfumes for its ability to enhance and prolong the scent of other fragrance components. Its sweet, floral, and slightly fruity aroma contributes to creating a pleasant and long-lasting fragrance.
Used in the Food Industry:
Benzyl Benzyloxyacetate is used as a flavoring agent in the food industry to impart a sweet and fruity taste to various products. Its unique aroma adds depth and complexity to the flavor profile of food items, enhancing the overall sensory experience for consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 30379-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,7 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30379-54:
(7*3)+(6*0)+(5*3)+(4*7)+(3*9)+(2*5)+(1*4)=105
105 % 10 = 5
So 30379-54-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H16O3/c17-16(19-12-15-9-5-2-6-10-15)13-18-11-14-7-3-1-4-8-14/h1-10H,11-13H2

30379-54-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl Benzyloxyacetate

1.2 Other means of identification

Product number -
Other names benzyl 2-phenylmethoxyacetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30379-54-5 SDS

30379-54-5Relevant articles and documents

A novel VIVO-pyrimidinone complex: Synthesis, solution speciation and human serum protein binding

Gon?alves, Gisela,Tomaz, Isabel,Correia, Isabel,Veiros, Luís F.,Castro, M. Margarida C. A.,Avecilla, Fernando,Palacio, Lorena,Maestro, Miguel,Kiss, Tamás,Jakusch, Tamás,Garcia, M. Helena V.,Pessoa, Jo?o Costa

, p. 11841 - 11861 (2013/09/02)

The pyrimidinones mhcpe, 2-methyl-3H-5-hydroxy-6-carboxy-4-pyrimidinone ethyl ester (mhcpe, 1), 2,3-dimethyl-5-benzyloxy-6-carboxy-4-pyrimidinone ethyl ester (dbcpe, 2) and N-methyl-2,3-dimethyl-5-hydroxy-6-carboxyamido-4- pyrimidinone (N-MeHOPY, 3), are

Synthesis of 3-Deoxy-D-manno-2-octulosonic Acid (KDO)

Frick, Wendelin,Kruelle, Thomas,Schmidt, Richard R.

, p. 435 - 438 (2007/10/02)

triphenylphosphonium bromide (8), obtained from glyoxylic acid via a convenient one-pot procedure, reacted in a Wittig reaction with 4-O-benzyl-2,3:5,6-di-O-isopropylidene-D-mannose (7), readily synthesized on a large

Synthese et etude structurale d'alcoxy-8 et hydroxy-8 triazolo et pyrimidines

Sliwa, H.,Blondeau, D.,Rousseaux, O.

, p. 687 - 692 (2007/10/02)

8-Alkyloxytriazolo and pyrimidines were obtained by condensation of 5-alkoxy-4-hydrazinopyrimidines with ethyl orthoformate.When ethyl orthoacetate was used the corresponding derivatives bearing a methyl group on the triazole ring wer

Photolysis of Alkoxyacetic Acids in the presence of Mercury(II) Oxide and Iodine

Glover, Stephen A.,Golding, Stephen L.,Goosen, Andre,McCleland, Cedric W.

, p. 2479 - 2483 (2007/10/02)

Homolytic decarboxylation of a series of alkoxyacetic acids has furnished alkoxyalkyl alkoxyacetates when no substituents were present at the 2-position.Electron donating and withdrawing 2-substituents, with the exception of trichloromethyl, afforded products due to fragmentation of the alkoxyacetic acids.The reaction pathway is rationalised on the basis of the reactivity of the alkoxyalkyl iodide intermediates.

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