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16504-66-8

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16504-66-8 Usage

Description

(7Z)-dec-7-en-1-ol, also known as (E)-10-undecen-1-ol, is an unsaturated alcohol with the chemical formula C10H20O. It is a colorless liquid characterized by a floral, waxy odor. This organic compound is prominently utilized in various industries due to its distinctive properties and versatile applications.

Uses

Used in the Fragrance Industry:
(7Z)-dec-7-en-1-ol is used as a key component in the creation of perfumes and other cosmetic products. Its floral, waxy scent adds a unique and appealing fragrance to these products, enhancing their overall sensory experience for consumers.
Used as a Flavoring Agent:
In the food and beverage industry, (7Z)-dec-7-en-1-ol is employed as a flavoring agent to impart a distinct taste and aroma to various products. Its natural, pleasant odor makes it a popular choice for enhancing the flavor profile of different consumables.
Used in the Production of Synthetic Lubricants:
(7Z)-dec-7-en-1-ol is also utilized in the manufacturing process of synthetic lubricants. Its chemical properties make it a suitable additive for improving the performance and longevity of lubricants, contributing to better machinery operation and reduced wear and tear.
Used in Pest Control Products:
Due to its insecticidal properties, (7Z)-dec-7-en-1-ol is used in the development of pest control products. It serves as an effective agent in managing and controlling various types of insects, providing a valuable solution for agricultural and domestic applications.
Used as an Intermediate in Chemical Synthesis:
(7Z)-dec-7-en-1-ol plays a crucial role as an intermediate in the synthesis of various chemicals. Its versatile chemical structure allows for its use in the production of a wide range of compounds, further expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 16504-66-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16504-66:
(7*1)+(6*6)+(5*5)+(4*0)+(3*4)+(2*6)+(1*6)=98
98 % 10 = 8
So 16504-66-8 is a valid CAS Registry Number.

16504-66-8SDS

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 (Z)-dec-7-en-1-ol

1.2 Other means of identification

Product number -
Other names -

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:16504-66-8 SDS

16504-66-8Downstream Products

16504-66-8Relevant articles and documents

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Kita

, p. 436 (1957)

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General catalyst control of the monoisomerization of 1-alkenes to trans -2-alkenes

Larsen, Casey R.,Erdogan, Gulin,Grotjahn, Douglas B.

supporting information, p. 1226 - 1229 (2014/02/14)

After searching for the proper catalyst, the dual challenges of controlling the position of the double bond, and cis/trans-selectivity in isomerization of terminal alkenes to their 2-isomers are finally met in a general sense by mixtures of (C5Me5)Ru complexes 1 and 3 featuring a bifunctional phosphine. Typically, catalyst loadings of 1 mol % of 1 and 3 can be employed for the production of (E)-2-alkenes at 40-70 C. Catalyst comprising 1 and 3 avoids more than any other known example the thermodynamic equilibration of alkene isomers, as the trans-2-alkenes of both nonfunctionalized and functionalized alkenes are generated.

Nickel phthalocyanine assisted highly efficient and selective carbonyl reduction in polyethylene glycol-400

Verma, Praveen Kumar,Sharma, Upendra,Kumar, Neeraj,Bala, Manju,Kumar, Vishal,Singh, Bikram

experimental part, p. 907 - 913 (2012/10/07)

Nickel phthalocyanine with polyethylene glycol- 400 is described as a reusable green catalytic system for highly chemo- and regioselective reduction of carbonyl compounds to corresponding alcohols at room temperature. The catalytic system showed wide substrate scope covering aromatic, hetero aromatic and aliphatic carbonyl compounds with high turnover number and frequency. In the present study, 1,3- and 1,4-benzenedicarbaldehydes have been regioselectively reduced to corresponding alcohols for the first time. The catalyst was reused up to seven times without any significance loss in activity. Springer Science+Business Media, LLC 2012.

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