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Undecan-8-enol, also known as 8-undecen-1-ol, is a colorless liquid with a strong, floral odor. It is an organic compound belonging to the class of alkenols, characterized by the presence of a carbon-carbon double bond in its structure. The molecular formula for undec-8-enol is C11H22O, and it has a molecular weight of 170.29 g/mol. This chemical is primarily used in the fragrance industry as a scent component in various perfumes, soaps, and cosmetics due to its pleasant aroma. It can also be found in some natural essential oils, such as jasmine and ylang-ylang, contributing to their characteristic scents.

95008-94-9

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95008-94-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95008-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,0 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 95008-94:
(7*9)+(6*5)+(5*0)+(4*0)+(3*8)+(2*9)+(1*4)=139
139 % 10 = 9
So 95008-94-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O/c1-2-3-4-5-6-7-8-9-10-11-12/h3-4,12H,2,5-11H2,1H3/b4-3+

95008-94-9SDS

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 undec-8-en-1-ol

1.2 Other means of identification

Product number -
Other names 8-undecen-1-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:95008-94-9 SDS

95008-94-9Downstream Products

95008-94-9Relevant academic research and scientific papers

ABSOLUTE CONFIGURATIONS OF 9,10-EPOXYDODECANOIC ACIDS BIOSYNTHESIZED BY MICROSOMES FROM JERUSALEM ARTICHOKE TUBERS

Fahlstadius, Per

, p. 1905 - 1908 (2007/10/02)

9Z- and 9E-Dodecenoic acids were epoxidized by a microsome preparation from Jerusalem artichoke tuber to form cis- and trans-epoxydodecanoic acids, respectively.Steric analysis showed that (a) 78percent of the cis-9,10-epoxydodecanoic acid had the 9R,10S configuration and 22percent had the 9S,10R configuration and that (b) 57percent of the trans-9,10-epoxydodecanoic acid had the 9S,10S configuration and 43percent had the 9R,10R configuration.

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