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2,3-dimethyl-1,4-dioxaspiro[4.5]decane is a colorless liquid chemical compound with the molecular formula C8H14O2, featuring a unique spirocyclic structure. It is primarily recognized for its floral and citrus aroma, making it a valuable ingredient in the fragrance industry.

5413-48-9

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5413-48-9 Usage

Uses

Used in Fragrance Industry:
2,3-dimethyl-1,4-dioxaspiro[4.5]decane is used as a fragrance ingredient for its distinct floral and citrus scent, contributing to the creation of perfumes, colognes, and various scented personal care and household products.
Used in Solvent Applications:
In certain industrial applications, 2,3-dimethyl-1,4-dioxaspiro[4.5]decane may also serve as a solvent, although its use in this capacity is less common due to its primary role as a fragrance component.
Safety Considerations:
While 2,3-dimethyl-1,4-dioxaspiro[4.5]decane is not known to be harmful to the environment or to pose significant health risks when used according to safety guidelines, it is important to handle it with care due to its potential for causing skin and eye irritation. Proper safety precautions should be taken to minimize any adverse effects.

Check Digit Verification of cas no

The CAS Registry Mumber 5413-48-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5413-48:
(6*5)+(5*4)+(4*1)+(3*3)+(2*4)+(1*8)=79
79 % 10 = 9
So 5413-48-9 is a valid CAS Registry Number.

5413-48-9SDS

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 2,3-dimethyl-1,4-dioxaspiro[4.5]decane

1.2 Other means of identification

Product number -
Other names 2,3-dimethyl-1,4-dioxaspiro<4.5>decane

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:5413-48-9 SDS

5413-48-9Relevant academic research and scientific papers

Synthese d'acetals cycliques dans des conditions douces; Applications a l'acetalisation du chloramphenicol

Meslard, J. C.,Subira, F.,Vairon, J. P.,Guy, A.,Garreau, R.

, p. 84 - 89 (2007/10/02)

Acetalization of 1-2 and 1-3 diols, even as sterically crowded as chloramphenicol, by carbonyl derivatives with substituents of various sizes has been performed at room temperature under mild conditions, by using heterogeneous catalysis (sulfonated polystyrene) in the presence of molecular sieves.Several new acetals of chloramphenicol have thus been obtained in good yields, isolated and characterized.

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