10315-98-7

Basic information

• Product Name: N-ISOBUTYLMORPHOLINE
• Synonyms: Morpholine, 4-(2-methylpropyl)-;Morpholine, 4-isobutyl-;4-ISOBUTYLMORPHOLINE;N-ISOBUTYLMORPHOLINE;ISOBUTYLMORPHOLINE;4-(2-methylpropyl)-Morpholine
• CAS NO: 10315-98-7
• Molecular Formula: C₈H₁₇NO
• Molecular Weight: 143.23
• EINECS: 233-696-1
• Mol File: 10315-98-7.mol
• Article Data: 10

Chemical Properties

• Melting Point: -9.9°C
• Boiling Point: 62-63°C 15mm
• Flash Point: 47°C
• Appearance: /
• Density: 0,89 g/cm3
• Vapor Pressure: 0.939mmHg at 25°C
• Refractive Index: n20/D 1.439
• CAS DataBase Reference: N-ISOBUTYLMORPHOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: N-ISOBUTYLMORPHOLINE(10315-98-7)
• EPA Substance Registry System: N-ISOBUTYLMORPHOLINE(10315-98-7)

Safety Data

• Hazard Codes: Xi
• Statements: 10-36/37/38
• Safety Statements: 16-26-36
• RIDADR: 1993
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 10315-98-7(Hazardous Substances Data)

Usage

General Description

N-Isobutylmorpholine is a chemical compound that is used as a corrosion inhibitor and as a selective surfactant in oil and gas production. It is a substituted morpholine derivative that is commonly used in water-based drilling fluids to prevent corrosion of metal equipment in oil and gas wells. It functions by forming a protective film on metal surfaces, thereby preventing the corrosive action of water and other substances. N-Isobutylmorpholine is also used as an additive in industrial water treatment processes to prevent the formation of scale and corrosion in boilers and cooling systems.

InChI:InChI=1/C8H17NO/c1-8(2)7-9-3-5-10-6-4-9/h8H,3-7H2,1-2H3

Upstream product

• 110-91-8 morpholine 
• 78-84-2 isobutyraldehyde 
• 2403-55-6 4-(2-methyl-1-propenyl)morpholine 
• 1708-29-8 2,5-dihydrofuran 
• 78-81-9 isobutylamine 
• 78-77-3 Isobutyl bromide 
• 75-30-9 2-iodo-propane 
• 50-00-0 formaldehyd 
• 513-36-0 isobutyryl chloride 
• 18071-39-1 2-methyl-1-(4-morpholinyl)propan-1-one 
• 78-82-0 Isobutyronitrile 
• 78-83-1 2-methyl-propan-1-ol 

Relevant articles and documents

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Hydroboration and reduction of enamines. III. Reaction of exo enamines and endo enamines with diborane and sodium borohydride (Japanese)

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Ionic liquid/H2O-mediated synthesis of mesoporous organic polymers and their application in methylation of amines

Mesoporous Tr?ger's base-functionalized polymers (Meso-TBPs) were prepared using a sulfonic acid group functionalized ionic liquid/H2O system, with surface areas up to 431 m2 g-1 and pore sizes of 3-15 nm. Ir(ii) coordinated Meso-TBPs exhibited extraordinary catalytic performance in the N-methylation of amines using methanol.

Colloid and nanosized catalysts in organic synthesis: IX hydrogenation of enamines with hydrogen at atmospheric pressure

Hydrogenation of enamines with hydrogen at atmospheric pressure was performed using nickel nanoparticles as a catalyst. The reaction may be used to produce tertiary amines under mild conditions using an accessible catalyst.