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1,4-Butanediyl, 1-hydroxy-4,4-dimethyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64108-92-5

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64108-92-5 Usage

Type of compound

Synthetic organic building block

Applications

Production of various polymers and resins
Stabilizer and antioxidant in the manufacturing of plastics and rubbers
Creation of specialty chemicals and pharmaceuticals

Toxicity

Relatively low toxicity

Safety

Generally considered safe for use in industrial processes when handled according to standard safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 64108-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,0 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 64108-92:
(7*6)+(6*4)+(5*1)+(4*0)+(3*8)+(2*9)+(1*2)=115
115 % 10 = 5
So 64108-92-5 is a valid CAS Registry Number.

64108-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name γ-Methylvalerophenondiradikal

1.2 Other means of identification

Product number -
Other names -

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:64108-92-5 SDS

64108-92-5Relevant academic research and scientific papers

DOES INTERSYSTEM CROSSING IN TRIPLET BIRADICALS GENERATE SINGLETS WITH CONFORMATIONAL MEMORY?

Scaiano, J. C.

, p. 819 - 824 (1982)

The effect of temperature, concentration, external magnetic fields and paramagnetic quenchers on the lifetime of biradicals produced in the Norrish Type II reaction has been examined.Analysis of this data and that available from earlier reports leads to the conclusion that in addition to controlling the biradical lifetimes, intersystem crossing in triplet-derived biradicals plays a critical role in determining the behaviour and products which result from singlet biradical reactions.The effect is attributed to conformational memory in the singlet biradical which reflects its short lifetime.

UV-Laser Photochemistry: Trapping of the Norrish Type II Triplet Diradical 1-Hydroxy-4-methyl-1-phenyl-1,4-pentanediyl with Molecular Oxygen

Adam, Waldemar,Grabowski, Sven,Wilson, R. Marshall

, p. 561 - 564 (2007/10/02)

The triplet lifetime (3τ = 131+/-5 ns) of diradical 2, produced in the laser photolysis (334 nm) of 4-methyl-1-phenyl-1-pentanone (1) in methanol, was determined by dioxygen trapping.This lifetime agrees well with the value determined by laser flash photolysis (3τ = 97 ns), thereby establishing the reliability of the trapping technique.The trapping product was prepared by independent synthesis and characterized as 3-hydroxy-1,2-dioxolane 9, the ring tautomer of hydroperoxide 6. - Keywords: Norrish type II triplet diradical/ UV-Laser photochemistry

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