42370-07-0

Usage

Uses

Used in Industrial Cleaning:
CAMEK DH is used as a cleaning agent for heat exchangers and similar equipment, as it effectively dissolves and removes scale and rust deposits. The citric acid in the formulation aids in breaking down these deposits, ensuring a thorough cleaning process.
Used in Descaling Applications:
CAMEK DH is used as a descaling agent for heat exchangers, where ammonium bifluoride, a powerful cleaning agent, helps in removing tough mineral deposits that can hinder the performance of the equipment.
Used in Solvent Applications:
CAMEK DH is used as a solvent for organic contaminants, with methyl alcohol being a key component that helps dissolve and remove these contaminants, ensuring a clean and efficient operation of the equipment.
Used in pH Adjustment:
CAMEK DH is used as a pH adjuster in the cleaning process, with potassium hydroxide helping to maintain the optimal pH level for effective cleaning and descaling of heat exchangers and similar equipment.

InChI:InChI=1/C11H18O/c1-7(12)10-8-4-5-9(6-8)11(10,2)3/h8-10H,4-6H2,1-3H3

Upstream product

• 79-92-5 camphene 
• 13211-15-9 (+-)-camphenilone 
• 50705-16-3 3,3-dimethylbicyclo[2.2.1]heptane-2-carbaldehyde 
• 5001-70-7 Vinylnorcamphane 
• 66062-78-0 1-((1S,4R)-3,3-Dimethyl-bicyclo[2.2.1]hept-2-yl)-ethanol 
• 38359-48-7 ω-methyl camphene 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 542-92-7 cyclopenta-1,3-diene 
• 6090-21-7 ω-bromomethylcamphene 
• 54382-52-4 (E)-3-ethylidene-2,2-dimethylbicyclo<2.2.1>heptane 
• 15780-34-4 1-(3,3-Dimethyl-bicyclo<2.2.1>hept-2-yl)ethanon 
• 67-56-1 methanol 
• 92214-46-5 ω-iodo-ω-methylcamphene 
• 85506-67-8 endo-2,2-dimethylbicyclo<2.2.1>heptane-3-carboxylic acid 

Downstream Products

• 67519-00-0 2-exo-10-camphanoic acid 
• 15780-34-4 1-(3,3-Dimethyl-2-exo-norbornyl)-ethanone 
• 66062-78-0 exo-1-(3,3-Dimethyl-bicyclo<2.2.1>hept-2-yl)-ethanol 
• 18310-55-9 (3,3-dimethylbicyclo[2.2.1]heptan-2-yl)methanol 
• 79861-75-9 1-(3,3-Dimethyl-2-exo-bicyclo<2.2.1>heptyl)-2-bromethanon 
• 94201-14-6 4-(3,3-Dimethyl-2-exo-norbornyl)-2-methylbut-2-en-1-ol 
• 78925-02-7 ((1S,2R,4R)-3,3-Dimethyl-bicyclo[2.2.1]hept-2-yl)-hydroxy-acetyl chloride 
• 78924-96-6 2-(3',3'-Dimethyl-2'-exo-norbornyl)-2-hydroxyessigsaeurebenzylester 
• 515-28-6 (+/-)-2.2-Dimethyl-norbornanol-(3exo) 

Relevant academic research and scientific papers

CONFORMATION-SPECIFIC PHOTOCHEMISTRY IN ISOTROPIC LIQUID MEDIA: NORRISH TYPE II REACTIONS OF EPIMERIC 2-ACETYL-3,3-DIMETHYL NORBORNANES

The epimeric ketones 1 and 2 have been shown to display conformation-specific photobehaviour, especially in liquid media.

Synthesis in the Isocamphane Series, XXIV. The Synthesis of endo-Configurated Isocamphane Derivatives

The syntheses of 46 endo-configurated isocamphane derivatives starting from camphenilanic acid (1) are described.The endo-configuration of the new compounds at position 2 of the bicyclus was retained throughout as has been established by 1H-NMR spectroscopy. - Keywords: Camphenilanic acid; Bicycloheptane; Aldol reaction; Grignard reaction; Enones

Photochemistry of Vinyl Halides: Part I - Radical Versus Ionic Photobehaviour of Some Vinyl Halides Based on Camphene

A systematic study of the photochemical behaviour of a group of vinyl halides (1-5) incorporating bicyclo(2.2.1)heptane skeleton is reported.The various parameters that control the formation of radical and ionic products have been investigated.The quenching and sensitization studies reveal that the radical products are derived from the triplet excited states whereas the corresponding singlet excited states may be responsible for the ionic products.The ground-state (silver ion-assisted) solvolytic reactivity pattern of these vinyl halides has been correlated for the first time with their photobehaviour.A plausible mechanism based on electron transfer concept has been proposed.

ω-Methylcamphene/ω,ω-Dimethylcamphene: Synthesis and Reactions

ω-Methylcamphene (8)/ω,ω-Dimethylcamphene (9) have been synthesized by two routes; (i) the Prins reaction on camphene (1)/ω-methylcamphene (8) and (ii) olefination with methylenetriphenylphosphorane of the aldehyde (17)/methyl ketone (24) followed by isomerization of the resulting hydrocarbon with N-lithioethylenediamine.Camphenilone (2) also undergoes a direct Wittig reaction with ethylidenephosphorane (27) yielding 8 (E/Z)-mixture but fails to react with isopropylidenephosphorane (28) in an attempt to generate 9.Camphene (1) and its ω-methyl homologues 8/9 undergo normal epoxidation with perbenzoic acid without excess consumption of peracid.Lewis acid-catalyzed rearrangement of the resulting epoxides 16/23/29 has also been studied.The Hg(OAc)2/NaCl reaction on 8 yields the crystalline ω-methyl-ω-mercurichloride (10) transformed by pyridine perbromide into the ω-bromo-ω-methylcamphene (11).