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4433-36-7

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4433-36-7 Usage

Description

3,4,5,6-Tetrahydropseudoionone is an organic compound with a sweet, floral, balsamic odor and a rose to woody quality. It also has a sweet, fruity flavor, reminiscent of apple and peach. 3,4,5,6-TETRAHYDROPSEUDOIONONE is known for its pleasant and versatile scent and taste, making it a valuable ingredient in various industries.

Uses

Used in the Fragrance Industry:
3,4,5,6-Tetrahydropseudoionone is used as a fragrance ingredient for its sweet, floral, and balsamic scent with a rose to woody quality. It is particularly suitable for creating perfumes, colognes, and other scented products due to its pleasant and versatile aroma.
Used in the Flavor Industry:
In the flavor industry, 3,4,5,6-tetrahydropseudoionone is used as a flavoring agent for its sweet, fruity taste, which is somewhat similar to apple and peach. It is commonly utilized in the production of beverages, confectionery, and other food products to enhance their flavor profile and provide a pleasant taste experience.
Used in the Cosmetics Industry:
3,4,5,6-Tetrahydropseudoionone is also used in the cosmetics industry as an additive to provide a pleasant scent and taste to various cosmetic products, such as lotions, creams, and lip balms. Its sweet, floral, and balsamic odor, along with its fruity taste, makes it an ideal choice for enhancing the sensory experience of these products.
Used in the Pharmaceutical Industry:
In the pharmaceutical industry, 3,4,5,6-tetrahydropseudoionone may be used as an active ingredient or additive in the development of medications, particularly those that require a pleasant taste or scent to improve patient compliance. Its sweet, fruity flavor and floral, balsamic odor can make medications more palatable and enjoyable for patients to consume.

Preparation

By hydrogenation of pseudo-ionone with colloidal palladium; this reaction leads to a product with considerable mixture; also from linalool plus acetic anhydride and sodium ethoxide, followed by hydrogenation; another method starts with geraniol via the acid chloride.

Check Digit Verification of cas no

The CAS Registry Mumber 4433-36-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4433-36:
(6*4)+(5*4)+(4*3)+(3*3)+(2*3)+(1*6)=77
77 % 10 = 7
So 4433-36-7 is a valid CAS Registry Number.
InChI:InChI=1S/C13H24O/c1-11(2)7-5-8-12(3)9-6-10-13(4)14/h7,12H,5-6,8-10H2,1-4H3

4433-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,10-dimethyl-9-undecen-2-one

1.2 Other means of identification

Product number -
Other names 3,4,5,6-TETRAHYDROPSEDOIONONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:4433-36-7 SDS

4433-36-7Relevant articles and documents

Stepwise hydrogenation of specific isoprenoids

-

Page/Page column 8, (2016/02/29)

The present invention relates to a stepwise hydrogenation of specific isoprenoids of formula using a specific catalyst.

Process for the preparation of phytone and novel intermediates thereof

-

Example 2, (2010/01/31)

Novel intermediate compounds which can be used in the preparation of phytone and Vitamin E and a process for the preparation thereof. A process for the preparation of phytone from the intermediate compounds is also claimed.

Insect Growth Regulators XVIII. - The Syntheses of Doxyl Nitroxides Juvenoids

Szykula, Jerzy,Zabza, Andrzej

, p. 709 - 710 (2007/10/02)

Starting from pseudoionone (1), the juvenoids 7a and 7b were synthesized.

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