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(±)-2,6-dimethylhept-6-en-1-ol, also known as geraniol, is a monoterpenoid alcohol with a sweet, floral aroma. It is commonly found in essential oils such as rose, citronella, and geranium. Geraniol has a chemical structure consisting of a seven-carbon chain with a double bond and two methyl groups, making it a versatile compound with varied industrial and medicinal applications.

36806-46-9

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36806-46-9 Usage

Uses

Used in Fragrance and Flavor Industry:
Geraniol is used as a key component in perfumes, soaps, and lotions due to its sweet, floral aroma.
Used in Pharmaceutical Applications:
Geraniol is used as an anti-inflammatory, antioxidant, and antimicrobial agent due to its potential pharmaceutical properties.
Used in Pest Control Products:
Geraniol is used as an insect repellent in various pest control products due to its insect repellent properties.

Check Digit Verification of cas no

The CAS Registry Mumber 36806-46-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,0 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36806-46:
(7*3)+(6*6)+(5*8)+(4*0)+(3*6)+(2*4)+(1*6)=129
129 % 10 = 9
So 36806-46-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-8(2)5-4-6-9(3)7-10/h5,9-10H,4,6-7H2,1-3H3

36806-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dimethylhept-6-en-1-ol

1.2 Other means of identification

Product number -
Other names (±)-2,6-DIMETHYLHEPT-6-EN-1-OL

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:36806-46-9 SDS

36806-46-9Downstream Products

36806-46-9Relevant academic research and scientific papers

Ring-closing olefin metathesis reactions; Synthesis of iso-β-bisabolol

M?rgenthaler, Jutta M.,Spitzner, Dietrich

, p. 1171 - 1172 (2004)

A ring-closing olefin metathesis is the key step in a synthesis of the rare iso-β-bisabolol found in sandalwood oils.

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