2-(2-Methylpropyl) quinoline

2-(2-Methylpropyl) quinoline

CAS Number
93-19-6
Molecular Formula
C13H15N
Purity
≥ 98.0% to ≥ 99% (Exclusive Perfumery & Pharma Grade)
Quinoline DerivativesNitrogenous Aroma ChemicalHeterocyclic IntermediatesSpecialty Corrosion InhibitorsHigh purity IBQ fragrance gradeAnalytical standard 2-isobutylquinolineC13H15N quinoline building block2-position alkylated quinolinesIsomers isobutyl quinolineBulk CAS 1333-53-5 supplierWholesale 2-(2-methylpropyl)quinoline

About 2-(2-Methylpropyl) quinoline

2-(2-Methylpropyl)quinoline, commonly known in the aroma industry as Isobutyl Quinoline (IBQ), is a powerful nitrogen-based heterocycle and a legendary "character" ingredient in perfumery and pharmaceutical synthesis. 2-Isobutylquinoline (CAS 93-19-6) is the structurally defined, high-purity version of the quinoline fa...

2-(2-Methylpropyl) quinoline Specifications

CAS Number
93-19-6
Molecular Formula
C13H15N
Molecular Weight
185.27
IUPAC NameORBotanical Name
2-(2-methylpropyl)quinoline
Canonical SMILES
CC(C)CC1=NC2=CC=CC=C2C=C1
InChI Key
FAQVGPWFQGGIPP-UHFFFAOYSA-N
EINECS Number
202-227-2
Molecular Weight
185.27
Boiling Point (Experimental)
148-150 °C Press: 14 Torr
Density (Predicted)
1.012+0.06 g/cm Temp: 25°C; Press: 760 Torr
pKa (Predicted)
5.417+0.10 Most Basic Temp: 25°C
Purity
≥ 98.0% to ≥ 99% (Exclusive Perfumery & Pharma Grade)
Appearance
Colorless to brownish-yellow liquid
Odor Profile
Intense leather, earthy, mossy, animalic, with "rooty" undertones
Specific Gravity
0.992-1.002 @ 25°C
HS Code
H411, H333, H320, H315, H302

Leather & Chypre Accords

Gold standard for creating authentic leather, suede, and tobacco notes in masculine and unisex fine fragrances

Fixative Properties

Powerful fixative, anchoring more volatile top notes and providing a long-lasting, sophisticated dry-down

CNS & Anti-Inflammatory Research

Privileged scaffold used by scientists to design molecules for Alzheimer’s research and anti-plasmodial activity

Bio-Active Linkers

Synthesis of specialized ligands for transition-metal catalysis and molecular imaging probes

Corrosion Inhibition

Ability to form protective films on metal surfaces in acidic environments, particularly in high-temperature oil and gas extraction in Industrial & Metallurgy applications

Rare Earth Element (REE) Recovery

Extractants in the separation of heavy metals from ores. The 2-position substitution prevents unwanted complexation with smaller, non-target ions

Targeted Drug Design

Scaffold for molecules targeting Type 2 Diabetes and various bacterial infections

Stereoselective Catalysis

Precursor for chiral ligands where the spatial orientation of the isobutyl group at the 2-position is mandatory for catalyst efficiency

2-(2-Methylpropyl) quinoline FAQs

Minimum Order Quantity

25 kg (pilot) · 1 MT (commercial)

Lead Time

3 – 5 weeks ex-works

Incoterms

FOB · CIF

Packaging

20 L pails, 200 L HDPE drums, 1000 L IBC

Regional Availability

India · EU · Middle East · Southeast Asia

Documentation

SDS · COA · TDS available on request

Compliance & Quality

REACH registered*

GHS/SDS available

ISO 9001:2015 site*

RoHS compliant*

Global sourcing network

Consistent quality & reliability

End-to-end technical support

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