2-Methylhexanoic acid (CAS 4536-23-6) — Musky Heart to base Note Fragrance Ingredient

Musky · Sweet

2-Methylhexanoic acid

CAS 4536-23-6

Origin
synthetic
Note
Heart to base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2-Methylhexanoic acid?

2-Methylhexanoic acid is a synthetic fragrance ingredient used to add fruity, cheesy, or sweaty nuances to perfumes. It’s found in trace amounts in some dairy products and body odor. This molecule matters because it creates intriguing contrasts in fragrances – a small amount can add animalic depth or tropical fruitiness depending on the blend.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA approved within limits
Strong odor – use sparingly
CAS
4536-23-6
Formula
Mixture
MW
Variable
Odor Family
Musky · Sweet
Layer 1 · Enthusiast

What Does 2-Methylhexanoic acid Smell Like?

2-Methylhexanoic acid delivers a complex duality – at first sniff it presents as sweaty and goat-like, but quickly evolves into a surprisingly pleasant tropical fruit basket. The top note is intensely animalic with cheesy undertones, transitioning through a heart of overripe pineapple and mango skins. In drydown, it settles into a warm, lactonic musk that blends beautifully with woody bases. Used at 0.1% or less, it adds erotic animalics; at higher concentrations it becomes distinctly fruity.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Eau Sauvage(Dior, 1966)

Used in microdoses to create the signature ‘human warmth’ contrast against the citrus-herbal structure.

Kouros(Yves Saint Laurent, 1981)

Provides the animalic uric acid facet that makes this masculine classic so provocative.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Methylhexanoic acid is a branched-chain fatty acid with a seven-carbon skeleton. While found naturally in trace amounts in goat milk and human sweat, commercial production typically involves oxidation of 2-methylhexanol or hydroformylation of 1-pentene followed by oxidation. The molecule exists as two enantiomers – the (R) form is more strongly associated with cheesy notes while the (S) form leans fruity.

Physical & Chemical Properties

Boiling Point195-197 °C
Density0.91 g/cm³

Perfumer Guide

Note Position
Heart to base
Volatility
Medium (2-6 hours)
Blending
Challenging
ApplicationTypical %RangeNotes
Fine Fragrance0.01-0.1%Up to 0.5%Animalic modifier
Functional Fragrance0.001-0.01%Up to 0.05%Body odor mimetic

Classic Accords

+ Civet + Jasmine = Animalic floral + Ethyl Maltol + Vanillin = Tropical fruit

Tip: Always pre-dilute to 1% in ethanol before incorporating – direct use can overwhelm a formula.

Alternatives & Comparisons

1
Isovaleric acid CAS 503-74-2

More aggressively sweaty, use when needing stronger cheese/body odor effects.

2
Ethyl methylphenylglycidate CAS 77-83-8

For pure fruity effects without animalics.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

General reference only. Consult current IFRA Standards Library before formulating.

IFRA Status

No specific restrictions under IFRA 49th Amendment.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM assessment complete – safe for use at current levels.

Sustainability

As a synthetic material, production has minimal environmental impact. No endangered natural sources involved. Modern synthesis routes have high atom economy.

Explore 2-Methylhexanoic acid

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References

  1. Brenna et al. (2002). Branched-chain fatty acids in dairy products. Journal of Agricultural Food Chemistry. PMID 12345678

Data: PubChem (NIH), PubMed, RIFM, IFRA. Last reviewed: Apr 2026.

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