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1-[1,1-bis(pentyloxy)ethoxy]pentane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7505-07-9

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7505-07-9 Usage

Type of compound

Ether

Physical state at room temperature

Hydrocarbon liquid

Usage

a. Solvent in industrial and research settings
b. Raw material for producing chemicals (surfactants, emulsifiers)
c. Potential applications in pharmaceutical and personal care industries

Solvency properties

Utilized in various applications due to its ability to dissolve other substances

Flammability

Flammable, requires careful handling and well-ventilated area for safety

Safety precautions

Handle with care, ensure proper ventilation during use

Check Digit Verification of cas no

The CAS Registry Mumber 7505-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7505-07:
(6*7)+(5*5)+(4*0)+(3*5)+(2*0)+(1*7)=89
89 % 10 = 9
So 7505-07-9 is a valid CAS Registry Number.

7505-07-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(1,1-dipentoxyethoxy)pentane

1.2 Other means of identification

Product number -
Other names tripentyl orthoacetate

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:7505-07-9 SDS

7505-07-9Relevant academic research and scientific papers

Transesterification of trimethyl orthoacetate: An efficient protocol for the synthesis of 4-alkoxy-2-aminothiophene-3-carbonitriles

Venkata Rao,Balakumar,Lakshmi Narayana,Pran Kishore,Rajwinder,Raghuram Rao

supporting information, p. 1274 - 1278 (2013/03/13)

A facile one-pot method is reported for the synthesis of 4-alkoxy-2-aminothiophene-3-carbonitriles. Transesterification of trimethylorthoacetate technique allowed introducing alkoxy substituents into 2-aminothiophene ring system. Diverse alkoxy substituents could be introduced efficiently by using this methodology. Further the synthesis of some of new 4-alkylamino-2-aminothiophenes is also reported.

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