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1,1,4,7-Tetramethylindane, with the molecular formula C14H20, is a colorless liquid characterized by a faint, sweet odor. It is insoluble in water and is recognized for its relatively low toxicity, being non-mutagenic and non-carcinogenic. This versatile chemical compound is utilized in various industrial applications, particularly within the fragrance and cosmetic sectors.

1078-04-2

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1078-04-2 Usage

Uses

Used in Fragrance and Cosmetic Industries:
1,1,4,7-Tetramethylindane is used as a fragrance ingredient in the production of perfumes and cosmetic products. Its sweet odor makes it a valuable addition to these products, enhancing their sensory appeal and consumer experience.
Used in Solvent Applications:
In the manufacturing process of polishes, paints, and coatings, 1,1,4,7-Tetramethylindane serves as a solvent. Its ability to dissolve other substances makes it a crucial component in the formulation of these products, contributing to their effectiveness and performance.
Safety Precautions:
1,1,4,7-Tetramethylindane should be handled and stored in a well-ventilated area to minimize any potential health risks. Additionally, it is essential to keep it away from sources of ignition to prevent any hazardous situations. By adhering to these safety measures, the compound can be safely and effectively utilized in its various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1078-04-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,7 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1078-04:
(6*1)+(5*0)+(4*7)+(3*8)+(2*0)+(1*4)=62
62 % 10 = 2
So 1078-04-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H18/c1-9-5-6-10(2)12-11(9)7-8-13(12,3)4/h5-6H,7-8H2,1-4H3

1078-04-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,7-tetramethyl-1,2-dihydroindene

1.2 Other means of identification

Product number -
Other names 1H-Indene, 2,3-dihydro-1,1,4,7-tetramethyl-

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:1078-04-2 SDS

1078-04-2Downstream Products

1078-04-2Relevant academic research and scientific papers

A copper(II) triflate-catalyzed tandem friedel-crafts alkylation/ cyclization process towards dihydroindenes

Zhang, Yugen,Chen, Liwei,Lu, Ting

supporting information; experimental part, p. 1055 - 1060 (2011/07/09)

A one-pot synthesis of dihydroindenes from substituted benzenes and haloalkenes was developed. The reaction proceeded via a copper(II) triflate [Cu(OTf)2]-catalyzed tandem Friedel-Crafts alkylation/cyclization process with high efficiency under

Diaminoindane derivatives

-

, (2008/06/13)

The invention relates to diaminoindane derivatives represented by the following formula: STR1 wherein R1 and R2 are each selected from the group consisting of a hydrogen atom and a lower alkyl group having from 1 to 4 carbon atoms, and a process for preparing same.

1,1,4,7-Tetramethyl-3-indanone, product produced thereby and organoleptic uses thereof

-

, (2008/06/13)

Described is a process for producing 1,1,4,7-tetramethyl-3-indanone defined according to the structure: STR1 the 1,1,4,7-tetramethyl-3-indanone per se and organoleptic uses thereof in augmenting or enhancing the aroma of perfume compositions, perfumed articles and colognes.

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