2-Methylvaleric acid (CAS 97-61-0) — Musky Base Note Fragrance Ingredient

Musky · Balsamic

2-Methylvaleric acid

CAS 97-61-0

Origin
synthetic
Note
Base
IFRA
Use with awareness
Data as of: Apr 2026

What Is 2-Methylvaleric acid?

2-Methylvaleric acid is a synthetic fragrance ingredient that adds cheesy, sweaty, or animalic notes to perfumes. It’s found in trace amounts in some dairy products and fermented foods. This molecule matters because it creates bold, unconventional accords when used skillfully in niche fragrances, adding a raw, human-like quality that contrasts beautifully with florals and woods.

Safety Profile

USE WITH AWARENESS
Generally safeUse with awarenessProfessional use
IFRA-approved with limits
Strong odor requires careful dosing
CAS
97-61-0
Formula
Mixture
MW
Variable
Odor Family
Musky · Balsamic
Layer 1 · Enthusiast

What Does 2-Methylvaleric acid Smell Like?

2-Methylvaleric acid unleashes an intense, primal aroma – imagine aged parmesan rind dissolving into warm human skin. The initial burst is aggressively cheesy with sweaty undertones, morphing into a leathery-animalic heart that clings to skin like well-worn suede. In drydown, it reveals a surprisingly soft muskiness when diluted, like the ghost of goat hair on a summer breeze. Used above 0.1%, it dominates; below 0.01%, it adds elusive animalic depth.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Secretions Magnifiques(Etat Libre d’Orange, 2006)

This controversial fragrance uses 2-methylvaleric acid at the threshold of perception to create its infamous ‘bodily fluids’ accord, blending with marine notes for a shocking yet compelling realism.

Muscs Koublai Khan(Serge Lutens, 1998)

The acid’s sweaty facets amplify the animalic musk core, creating a scent that evolves from intimate skin warmth to regal fur-lined opulence.

Layer 2

2D Molecular Structure

2-Methylpentanoic acid

SMILES: CCCC(C)C(O)=O

Chemistry, Properties & Perfumer Guide

The Chemistry

2-Methylvaleric acid is a branched-chain fatty acid with the molecular formula C6H12O2. It’s synthesized through oxidation of 2-methylpentanol or via Grignard reactions. The molecule’s stereochemistry significantly impacts its odor profile – the (R)-enantiomer is notably more sweaty and intense than the (S)-form. Industrially, it’s produced through hydrocarboxylation of 1-pentene followed by isomerization.

Physical & Chemical Properties

Boiling Point196-198 °C
Density0.925 g/cm³
Vapor Pressure0.3 mmHg at 25°C

Perfumer Guide

Note Position
Base
Volatility
Very low (hours-days)
Blending
Challenging
ApplicationTypical %RangeNotes
Fine Fragrance0.001-0.01%Up to 0.1%Animalic modifier
Functional FragranceNot usedN/AToo potent for most applications

Classic Accords

+ Civet + Castoreum = Animalic base + Jasmine + Honey = Animalic floral + Oakmoss + Leather = Vintage chypre

Tip: Always pre-dilute to 1% in ethanol before incorporating to prevent overwhelming blends.

Alternatives & Comparisons

1
Isovaleric acid CAS 503-74-2

More cheesey/ranky, less sweaty. Use when seeking sharper dairy notes rather than skin-like musky effects.

2
3-Methyl-2-hexenoic acid CAS 24694-09-9

Softer, more floral animalic musk with better blending properties for mainstream applications.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under IFRA standards. Self-limiting due to odor potency.

GHS Classification

H315 Skin irritation H319 Eye irritation

RIFM Assessment

RIFM evaluation complete – safe for use in current practices at reported levels.

Sustainability

As a synthetic material, 2-methylvaleric acid has minimal environmental impact in production. Its extreme potency means minuscule quantities are used, reducing resource consumption. Some perfumers seek natural analogs from microbial fermentation of dairy byproducts, though these lack consistency.

Explore 2-Methylvaleric acid

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References

  1. Brenna et al. (2003). Odor detection thresholds of branched fatty acids. Chemical Senses. PMID 12644696

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

Report a data error

Physicochemical Properties

DTXSID: DTXSID9021633

Physical Properties

Molecular Weight 116.16 g/mol🔬 EPA CompTox
Density 0.923 g/cm^3🔬 EPA CTX
Boiling Point 196.25 °C🔬 EPA CTX
Melting Point -85 °C🔬 EPA CTX
Flash Point 91.563 °C🔬 EPA CTX
Refractive Index 1.425 Dimensionless📊 OPERA
Molar Volume 122.578 cm^3/mol📊 OPERA

Partition & Solubility

LogP (Octanol-Water) 29.556 Log10 unitless🔬 EPA CTX
LogD (pH 5.5) 1.109 Log10 unitless📊 OPERA
LogD (pH 7.4) -0.667 Log10 unitless📊 OPERA
LogKoa (Octanol-Air) 4.76 Log10 unitless📊 OPERA
Water Solubility 0.129 mol/L🔬 EPA CTX
Henry's Law Constant 0 atm-m3/mole📊 OPERA

Transport Properties

Vapor Pressure 1.5 mmHg🔬 EPA CTX
Viscosity 2.724 cP📊 OPERA
Surface Tension 28.633 dyn/cm📊 OPERA
Thermal Conductivity 140.815 mW/(m*K)📊 OPERA

Molecular Descriptors

Topological Polar Surface Area 37.3 Ų💻 Computed
H-Bond Donors 1 count💻 Computed
H-Bond Acceptors 1 count💻 Computed
Rotatable Bonds 3 count💻 Computed
Aromatic Rings 0 count💻 Computed
Molar Refractivity 31.369 cm^3/mol📊 OPERA
Polarizability 12.436 Å^3📊 OPERA

Data Sources:

🔬 EPA Experimental data from U.S. EPA CompTox Chemicals Dashboard & CTX APIs. 📊 OPERA Predicted using EPA's OPERA QSAR models. 💻 Computed Calculated from SMILES using RDKit.

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