Welcome to LookChem.com Sign In|Join Free
  • or
2,3-DIMETHYL-5-HEXEN-3-OL is a chemical compound with the molecular formula C8H16O. It is a colorless and clear liquid with a strong odor, known for its pleasant aroma and versatile applications across different industries.

19550-90-4

Post Buying Request

19550-90-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

19550-90-4 Usage

Uses

Used in Food Industry:
2,3-DIMETHYL-5-HEXEN-3-OL is used as a flavoring agent for its fruity and floral flavor profiles, enhancing the taste and aroma of various food products.
Used in Perfume and Fragrance Industry:
2,3-DIMETHYL-5-HEXEN-3-OL is used as a key ingredient in perfumes and fragrances due to its strong and pleasant odor, contributing to the overall scent profile of these products.
Used in Insect Repellent Formulation:
2,3-DIMETHYL-5-HEXEN-3-OL is used as an insecticidal agent in the formulation of insect repellents, providing protection against insects and their bites.
Used in Cosmetics and Personal Care Products:
2,3-DIMETHYL-5-HEXEN-3-OL is used in the production of various cosmetics and personal care products, adding to their fragrance and potentially providing other functional benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 19550-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,5,5 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19550-90:
(7*1)+(6*9)+(5*5)+(4*5)+(3*0)+(2*9)+(1*0)=124
124 % 10 = 4
So 19550-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-5-6-8(4,9)7(2)3/h5,7,9H,1,6H2,2-4H3

19550-90-4SDS

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 2,3-dimethylhex-5-en-3-ol

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-hex-5-en-3-ol

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:19550-90-4 SDS

19550-90-4Relevant academic research and scientific papers

Allylation and crotylation of ketones and aldehydes using potassium organotrifluoroborate salts under lewis acid and montmorillonite k10 catalyzed conditions

Nowrouzi, Farhad,Thadani, Avinash N.,Batey, Robert A.

supporting information; experimental part, p. 2631 - 2634 (2009/10/02)

Two convenient highly diastereoselective protocols for the allylation and crotylation of ketones using practical, air- and water-stable potassium allyl and crotyltrifluoroborate salts have been developed. BF3-OEt 2 and montmorillonit

Synthesis of homoallylic alcohols from ketones in water

Wang, Jun,Yuan, Gu

, p. 401 - 405 (2007/10/03)

Homoallylic alcohols have been prepared in good yields by allylation of ketones with allyl bromide in the presence of stannous chloride dihydrate, zinc iodide, and ammonium chloride in water. Copyright Taylor & Francis LLC.

Allylic tin(IV)-tin(II) chloride-acetonitrile as a novel system for allylation of carbonyls or imines

Yasuda, Makoto,Sugawa, Yoshihiro,Yamamoto, Akihiro,Shibata, Ikuya,Baba, Akio

, p. 5951 - 5954 (2007/10/03)

Effective allylation of aldehydes, ketones and imines was accomplished by allylic tributyltins 1 in the presence of SnCl2 in an acetonitrile solution. In this reaction system, Sn(IV)-Sn(II) transmetallation must play a key role, generating the

Preparation and Stereochemistry of Some 1,1-Disubstituted Buta-1,3-dienes

Curry, Michael J.,Stevens, D.R.

, p. 1756 - 1760 (2007/10/02)

The preparation of five (E)- and five (Z)-1,1-disubstituted buta-1,3-dienes is described and their stereochemistry assigned.The effect of the Z-E isomerism on the chemical shifts in the 13C and 1H n.m.r. spectra is discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 19550-90-4