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4,4-Dimethylhexanal is an organic compound with the chemical formula C8H16O. It is a colorless liquid with a strong, pungent odor and is classified as an aldehyde. 4,4-Dimethylhexanal is primarily used as a fragrance ingredient in the perfumery industry, as well as a flavoring agent in food and beverage products. It is synthesized through various chemical reactions, such as the oxidation of 4,4-dimethylhexanol or the condensation of acetone with butyraldehyde. Due to its reactive nature, 4,4-dimethylhexanal can be further transformed into other compounds, such as 4,4-dimethylhexanol or 4,4-dimethylhexanoic acid, through reduction or oxidation processes.

5932-91-2

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5932-91-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5932-91-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 2 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5932-91:
(6*5)+(5*9)+(4*3)+(3*2)+(2*9)+(1*1)=112
112 % 10 = 2
So 5932-91-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16O/c1-4-8(2,3)6-5-7-9/h7H,4-6H2,1-3H3

5932-91-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4-dimethylhexanal

1.2 Other means of identification

Product number -
Other names Hexanal,4,4-dimethyl

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:5932-91-2 SDS

5932-91-2Downstream Products

5932-91-2Relevant academic research and scientific papers

Rhodium-catalysed hydroformylation of branched 1-alkenes; bulky phosphite vs. triphenylphosphine as modifying ligand

Van Rooy, Annemiek,De Bruijn, Jacques N. H.,Roobeek, Kees F.,Kamer, Paul C. J.,Van Leeuwen, Piet W. N. M.

, p. 69 - 73 (2007/10/03)

The influence of alkyl substituents in 1-alkene substrates in the rhodium-catalysed hydroformylation in the presence of tris(2-tertbutyl-4-methylphenyl) phosphite has been studied and compared with that observed for the reaction involving the conventional PPh3-modified catalyst. Hindered alkenes underwent hydroformylation at good rates (i.e. 1300 mol (mol Rh)-1 h-1 for 3,3-dimethyl-1-butene as T = 70°C and P = 20 bar (H2-CO)); under mild conditions the rates were only slightly affected by the alkyl substituents. The selectivity towards the linear aldehyde increases progressively with substitution, from 66% for 1-octene up to 100% for 3,3-dimethyl-1-butene, and the proportion of isomerized alkenes remained substantial (up to 17.4% for allylcyclohexane). The differences between the two systems are explained in terms of the different kinetics observed for them.

Heterocyclic pesticidal compounds

-

, (2008/06/13)

Compounds of the formula (I) STR1 which contain between 10 and 27 carbon atoms, and wherein m and n are independently selected from 0, 1 and 2; R2a is hydrogen, methyl, or ethyl; R2b is acetylene or contains between 3 and 18 carbon atoms and is a group R7, wherein R7 is a C1-13 non-aromatic hydrocarbyl group, optionally substituted by a cyano or C1-4 carbalkoxy group and/or by one or two hydroxy groups and/or by one to five halo atoms which are the same or different and/or by one to three groups R8 which are the same or different and each contain one to four hetero atoms, which are the same or different and are chosen from oxygen, sulphur, nitrogen and silicon, 1 to 10 carbon atoms and optionally 1 to 6 fluoro or chloro atoms or R2b is a 6-membered aromatic ring substituted by cyano and/or by one to three groups R8 and/or by a group --C CH, --C C-R7 or C C-halo and/or by one to five halo atoms and/or by one to three C1-4 haloalkyl groups wherein R7 and R8 are as hereinbefore defined; R4 and R6 are the same or different and are chosen from hydrogen, methyl, trifluoromethyl or cyano; and R5 is hydrogen or methyl provided that R2b is not propyl or butyl are described which have pesticidal activity, particularly against arthropod pests. Pesticidal formulations containing the compounds of the formula (I), their use in the control of pests and method for their preparation are also disclosed.

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