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3,7,11-trimethyldodecan-3-ol, also known as 3,7,11-trimethyl-3-dodecanol, is a branched-chain alcohol with the molecular formula C15H32O. It is a colorless liquid with a molecular weight of 228.42 g/mol. This organic compound is characterized by the presence of three methyl groups (-CH3) attached to the dodecane (C12H26) carbon chain at the 3rd, 7th, and 11th positions, with a hydroxyl (-OH) group at the 3rd position. 3,7,11-trimethyldodecan-3-ol is commonly found in the pheromone secretions of certain insects, such as the bark beetle, and is used in the synthesis of various fragrances and perfumes due to its pleasant, musky odor. It is also used as a fixative in the perfume industry to stabilize and prolong the scent of other fragrances.

7278-65-1

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7278-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7278-65-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7278-65:
(6*7)+(5*2)+(4*7)+(3*8)+(2*6)+(1*5)=121
121 % 10 = 1
So 7278-65-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H32O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h13-14,16H,6-12H2,1-5H3

7278-65-1SDS

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 3,7,11-trimethyldodecan-3-ol

1.2 Other means of identification

Product number -
Other names 3-Dodecanol,3,7,11-trimethyl

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:7278-65-1 SDS

7278-65-1Downstream Products

7278-65-1Relevant academic research and scientific papers

Selective reduction of dienes/polyenes using sodium borohydride/catalytic ruthenium(III) in various liquid amide aqueous mixtures

Babler, James H.,Ziemke, David W.,Hamer, Robert M.

, p. 1754 - 1757 (2013/04/10)

An efficient method to effect selective reduction of several structurally diverse dienes and an unsymmetrical triene is reported. The reduction is facile at 0 °C in a liquid amide aqueous solution containing sodium borohydride in the presence of 15 mol % ruthenium(III) chloride. The chemoselectivity of the reaction is controlled by proper choice of the liquid amide solvent.

Hydrogenation on granular palladium-containing catalysts: I. Hydrogenation of tertiary acetylene alcohols

Tolkacheva,Kislyi,Taits,Semenov

, p. 150 - 152 (2007/10/03)

Commercial granular palladium catalyst (0.5% of Pd on γ-Al 2O3) was modified by treating with zinc acetate (type 1) or successively with zinc acetate and ammonia (type 2). The treatment significantly increased the hydrogenation selectivity for a triple bond into a double bond: to 85.3-93.1% with the type 1 catalyst and to 96.3-97.8% with the type 2 catalyst. A construction of an autoclave with a fixed bed of the granular catalyst is described.

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