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3-Phenylundecane is an organic compound with the molecular formula C17H26. It is a colorless liquid at room temperature and has a distinct aromatic odor. This alkane consists of an undecane chain (a hydrocarbon chain with 11 carbon atoms) with a phenyl group (a benzene ring) attached to the third carbon atom. 3-Phenylundecane is insoluble in water but soluble in organic solvents such as ethanol and ether. It is primarily used as a solvent, a chemical intermediate in the synthesis of various compounds, and as a component in the formulation of fragrances and flavors. Due to its relatively low toxicity, it is considered safe for use in these applications.

4536-87-2

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4536-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4536-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,3 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4536-87:
(6*4)+(5*5)+(4*3)+(3*6)+(2*8)+(1*7)=102
102 % 10 = 2
So 4536-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H28/c1-3-5-6-7-8-10-13-16(4-2)17-14-11-9-12-15-17/h9,11-12,14-16H,3-8,10,13H2,1-2H3

4536-87-2SDS

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 undecan-3-ylbenzene

1.2 Other means of identification

Product number -
Other names 3-Phenyl-undecan

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:4536-87-2 SDS

4536-87-2Downstream Products

4536-87-2Relevant academic research and scientific papers

Process for the production of phenylalkanes using a hydrocarbon fraction that is obtained from the Fischer-Tropsch process

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Page/Page column 4, (2008/06/13)

A process for the production of phenylalkanes comprising a reaction for alkylation of at least one aromatic compound by at least one hydrocarbon fraction that is directly obtained from the Fischer-Tropsch process comprising linear olefins that have 9 to 16 carbon atoms per molecule and oxygenated compounds is described. Said alkylation reaction is carried out in a catalytic reactor that contains at least one reaction zone that comprises at least one acidic solid catalyst, and said hydrocarbon fraction does not undergo any purification treatment prior to its introduction into said reaction zone.

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