Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched alkyl esters (CAS 125643-61-0) — Citrus N/A Note Fragrance Ingredient

Citrus · Floral

Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched alkyl esters

CAS 125643-61-0

Origin
synthetic
Note
N/A
IFRA
Professional use
Data as of: Apr 2026

What Is Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched alkyl esters?

This synthetic compound is used as a stabilizer and antioxidant in various industrial applications, including plastics and rubber. Consumers may encounter it indirectly in durable goods rather than personal care products. Its primary function is to prevent degradation of materials rather than contribute fragrance, though it may have subtle odor characteristics at high concentrations.

Safety Profile

PROFESSIONAL USE
Generally safeUse with awarenessProfessional use
Industrial chemical – not for fragrance use
No safety data for topical applications
CAS
125643-61-0
Formula
Mixture
MW
Variable
Odor Family
Citrus · Floral
Layer 1 · Enthusiast

What Does Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched alkyl esters Smell Like?

This material is not characterized as a fragrance ingredient and lacks significant odor properties at typical use levels. At elevated concentrations, it may present faint phenolic or waxy notes due to its hindered phenol structure, but these are not considered desirable in perfumery. The molecule’s primary function is chemical stabilization rather than olfactive contribution.

Layer 2

Chemistry, Properties & Perfumer Guide

The Chemistry

This compound belongs to the class of hindered phenol antioxidants, featuring tert-butyl groups at the 3 and 5 positions of the aromatic ring. The esterification with C7-9 branched alkyl chains enhances its compatibility with polymeric matrices. Industrial synthesis typically involves Friedel-Crafts alkylation of phenol followed by esterification. The sterically hindered structure prevents hydrogen abstraction that leads to oxidative degradation in substrates.

Physical & Chemical Properties

Primary UsePolymer stabilizer
ApplicationIndustrial materials

Perfumer Guide

Note Position
N/A
Volatility
N/A
Blending
N/A
ApplicationTypical %RangeNotes
Industrial0.1-1%Up to 2%Polymer stabilization

Classic Accords

Tip: Not recommended for fragrance applications.

Alternatives & Comparisons

Layer 3

Safety, Regulatory & Sustainability

⚠ Regulatory Disclaimer

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

IFRA Status

Not evaluated by IFRA – industrial use only.

RIFM Assessment

No RIFM evaluation – not a fragrance material.

Sustainability

As an industrial antioxidant, this material is produced synthetically from petrochemical feedstocks. Its environmental impact relates primarily to manufacturing processes and end-of-life disposal in polymer applications. No natural alternatives exist for its specific technical function in material stabilization.

Explore Benzenepropanoic acid, 3,5-bis(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched alkyl esters

Browse essential oils and aroma compounds.

Browse on iHerb →

Affiliate disclosure: we may earn a small commission at no extra cost to you.

References

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

    Report a data error

    Similar Posts