Propyl isovalerate (CAS 557-00-6) — Sweet Top Note Fragrance Ingredient

Sweet · Citrus

Propyl isovalerate

CAS 557-00-6

Origin
synthetic
Note
Top
IFRA
Generally safe
Data as of: Apr 2026

What Is Propyl isovalerate?

Propyl isovalerate is a synthetic ester commonly used in fruity and apple-like fragrance compositions. You’ll encounter it in fresh, sweet perfumes and some flavorings. This ingredient matters because it adds a crisp, juicy quality to fragrances, mimicking natural fruit aromas while being more stable and consistent than natural extracts.

Safety Profile

GENERALLY SAFE
Generally safeUse with awarenessProfessional use
No known major safety concerns
Commonly used in food flavorings
CAS
557-00-6
Formula
Mixture
MW
Variable
Odor Family
Sweet · Citrus
Layer 1 · Enthusiast

What Does Propyl isovalerate Smell Like?

Propyl isovalerate bursts with a bright, fruity aroma reminiscent of green apples and ripe pears. The top note is intensely fresh, like biting into a just-picked Granny Smith apple with a hint of banana-like sweetness. As it evolves, it reveals a subtle creamy undertone, similar to pear drops candy, before drying down to a faint, clean fruitiness that lingers softly. The overall effect is juicy and uplifting without being cloying, making it perfect for creating naturalistic fruit accords.

Scent Profile

In Famous Fragrances

Fragrance associations may not reflect actual formulations.

Light Blue(Dolce & Gabbana, 2001)

Used to enhance the crisp apple note in this fresh aquatic fragrance, adding juicy realism to the citrus top notes while maintaining transparency.

Green Tea(Elizabeth Arden, 1999)

Provides subtle fruity lift to the citrus-green tea accord, creating a refreshing, slightly sweetened effect reminiscent of iced fruit tea.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

Propyl isovalerate is an ester formed from the condensation of propanol and isovaleric acid. As a synthetic material, it’s typically produced via acid-catalyzed esterification. The molecule’s simple structure (C8H16O2) gives it high volatility and excellent diffusion. While not found in significant quantities in nature, its fruity character makes it valuable for reconstructing apple and pear aromas. The ester’s stability and low molecular weight contribute to its bright, immediate olfactory impact.

Physical & Chemical Properties

Boiling Point~160-165 °C (estimated)
Density~0.86 g/cm³ (estimated)
SolubilitySlightly soluble in water, miscible with alcohols and oils

Perfumer Guide

Note Position
Top
Volatility
High (30-90 min)
Blending
Good
ApplicationTypical %RangeNotes
Fine Fragrance0.5-3%Up to 5%Fruity top note enhancement
Functional Fragrance0.1-1%Up to 2%Fresh fruit nuances in detergents
Flavorings10-50 ppmUp to 100 ppmApple/pear flavor modifier

Classic Accords

Tip: Use in trace amounts with citrus oils to create natural-seeming fruit effects without overwhelming the composition.

Alternatives & Comparisons

1
Ethyl isovalerate CAS 108-64-5

More volatile with sharper green apple character, useful when brighter top notes are needed.

2
Hexyl acetate CAS 142-92-7

Provides similar fruity effects but with more pear-like nuance and longer persistence.

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not restricted under current IFRA standards (Amendment 49).

RIFM Assessment

Considered safe for current fragrance use levels based on RIFM evaluation.

Sustainability

As a synthetic material, propyl isovalerate offers consistent quality without agricultural variability. Its production from petrochemical feedstocks raises some environmental considerations, but its high potency means only small quantities are needed compared to natural extracts. No known significant ecological toxicity at usage levels.

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References

  1. Burdock, G.A. (2010). Fenaroli’s Handbook of Flavor Ingredients. CRC Press.
  2. Arctander, S. (1969). Perfume and Flavor Chemicals. Allured Publishing.

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

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