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2-ISOBUTOXYETHYL BENZOATE is a chemical compound that belongs to the class of benzoate esters, characterized by its pleasant odor and low toxicity, making it suitable for use in various applications while adhering to safety regulations and guidelines.

5451-76-3

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5451-76-3 Usage

Uses

Used in Cosmetics and Personal Care Industry:
2-ISOBUTOXYETHYL BENZOATE is used as a fragrance ingredient for its pleasant odor, enhancing the sensory experience of cosmetics and personal care products.
Used in Industrial Applications:
2-ISOBUTOXYETHYL BENZOATE is used as a solvent in various industrial processes, leveraging its chemical properties to facilitate reactions or dissolve substances.

Check Digit Verification of cas no

The CAS Registry Mumber 5451-76-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5451-76:
(6*5)+(5*4)+(4*5)+(3*1)+(2*7)+(1*6)=93
93 % 10 = 3
So 5451-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O3/c1-2-3-9-15-10-11-16-13(14)12-7-5-4-6-8-12/h4-8H,2-3,9-11H2,1H3

5451-76-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-butoxyethyl benzoate

1.2 Other means of identification

Product number -
Other names NMBQBIACXMPEQB-UHFFFAOYSA

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:5451-76-3 SDS

5451-76-3Downstream Products

5451-76-3Relevant academic research and scientific papers

Ethylene glycol monobutyl ether benzoate and preparation method thereof

-

Paragraph 0015; 0020-0027, (2019/10/10)

The invention relates to a preparation method of ethylene glycol monobutyl ether benzoate. The ethylene glycol monobutyl ether benzoate is prepared from the raw materials of benzoic acid and ethylene glycol monobutyl ether at a molar ratio of 1:(1-5); the adding molar weight of a catalyst is 0.1-5% of the molar weight of the benzoic acid; quantitative benzoic acid, ethylene glycol monobutyl ether and catalyst are sequentially added into a tank reactor; the total volume of the materials accounts for 30-70% of the total volume of the tank reactor; the reactor is heated to 120-200 DEG C, and then a heat preservation reaction is carried out for 4-12 h; after the reaction is finished, the reactor is cooled to room temperature; the materials which complete the reaction and are cooled are subjected to vacuum rectification by passing through a plurality of rectifying towers in sequence, wherein the pressure in each rectifying tower is between minus 0.090 and minus 0.098 Mpa (G); an ethylene glycol monobutyl ether benzoate finished product is collected by the last rectifying tower in the entire rectification process. According to the ethylene glycol monobutyl ether benzoate and the preparation method thereof, the boiling point is high, no foreign smell exists, and the cost is low; the raw materials of the ethylene glycol monobutyl ether benzoate are simple, the preparation process is simple, the control is easy, the work efficiency is high, and the product quality is good.

A New Indirect Application of Aggregative Activation: Synthesis of Esters by Cobalt-Catalyzed Carbonylation of Aryl, Heterocyclic, and Vinyl Halides under Atmospheric Pressure

Marchal, Joel,Bodiguel, Jacques,Fort, Yves,Caubere, Paul

, p. 8336 - 8340 (2007/10/02)

Sun lamp illuminated alkoxycarbonylation of aryl, heteroaryl, and vinyl halides was performed under atmospheric pressure of CO in the presence of a cobalt catalyst in situ generated from Co(OAc)2.Illunination through a Pyrex flask was sufficient to catalyze the reaction.This process avoids the use of Co2(CO)8 and excess CH3I, which were required in the earlier procedure.A SRN1 mechanism is proposed.

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