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3441-74-5

Ethylium, 1-hydroxy-1-phenyl-, also known as 1-phenylethan-1-ol or phenethyl alcohol, is an organic compound with the chemical formula C8H10O. It is a colorless, oily liquid with a floral, rose-like odor. Phenethyl alcohol is widely used in the fragrance industry as a fixative and in the production of various perfumes, as well as in the flavor industry for its sweet, floral taste. It is also found in small amounts in natural sources such as roses, jasmine, and honey. The compound is synthesized through various methods, including the reduction of acetophenone and the reaction of ethylmagnesium bromide with benzaldehyde. Phenethyl alcohol is considered non-toxic and has been used in the pharmaceutical industry as a sedative and tranquilizer.

3441-74-5

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3441-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3441-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,4 and 1 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3441-74:
(6*3)+(5*4)+(4*4)+(3*1)+(2*7)+(1*4)=75
75 % 10 = 5
So 3441-74-5 is a valid CAS Registry Number.

3441-74-5SDS

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 1-phenyl-ethanone, protonated form

1.2 Other means of identification

Product number -
Other names Hydroxy-methyl-phenyl-carbonium

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:3441-74-5 SDS

3441-74-5Downstream Products

3441-74-5Relevant articles and documents

Proton affinity measurements using ion mobility spectrometry

Tabrizchi, Mahmoud,Shooshtari, Saeed

, p. 863 - 870 (2003)

Relative proton affinities are usually measured by means of high pressure mass spectrometry. In this work ion mobility spectrometry was used to determine proton affinities. The standard molar enthalpy change δHM0 for the reaction MH

Fragmentation of 1-hydroxy-2-(5H-dibenzo[a,d]cyclohepten-5-yl)-1-phenylethyl cation in superacid

Osadchii,Stanescu,Mamatyuk,Shubin

, p. 381 - 383 (2007/10/03)

The 1-hydroxy-2-(5H-dibenzo[a,d]cyclohepten-5-yl)-1-phenylethyl cation generated under "long life" conditions undergoes fragmentation to afford 5H-dibenzo[a,d]cycloheptenyl-and methylphenylhydroxycarbinyl cations but does not undergo carbocationic cycliza

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