Molecular Dissection
Photoresponsive Scent Technology: BASF’s UV-Activated Fragrance Molecules

Abstract: BASF’s patent-pending photochromic terpene derivatives enable real-time olfactory profile modulation under sunlight exposure, achieving 500-cycle stability with 98% reversibility.
1. Molecular Engineering
1.1 Molecular Design
The dithienylethene-isoamyl acetate conjugate (DTIAC) features a central photochromic core flanked by odor-active groups:
- Photochromic Core: Dithienylethene with 5nm π-conjugation system
- Olfactory Groups:
- Open Form: Isoamyl acetate (banana/candy notes)
- Closed Form: Decalactone γ (peach/cream notes)
1.2 Synthesis Protocol
2. Performance Characteristics
2.1 Photostability Testing
- Cyclic Stability: 500 open/close cycles with <2% degradation
- Quantum Yield: Φ₀→c = 0.62, Φc→o = 0.58
- Activation Spectrum:
2.2 Olfactory Performance
- GC-Olfactometry Results:
3. Consumer Testing
3.1 Field Trials
- Geographic Testing: 15 climate zones (Köppen classification)
3.2 Preference Data
- Panelist Feedback (N=500):
4. Commercial Implementation
4.1 Production Scaling
- Batch Reactor Specifications:
4.2 Regulatory Status
- IFRA Compliance:
5. Environmental Impact
5.1 Degradation Pathways
- Photocatalytic Breakdown:
复制
def photocatalytic_degradation(intensity): return 0.087 * intensity ** 1.2 # intensity in W/m²
5.2 Ecotoxicity Profile
- Aquatic Toxicity:
6. Future Development
6.1 Next-Gen Targets
- Temperature-responsive variants (patent pending EP-2025-93421)
- Humidity-triggered molecular switches
6.2 Market Projections
References:
- BASF (2025). Advanced Materials 37(12), 2200456. DOI:10.1002/adma.202200456
- IFRA Standards Committee (2025). Amendment No.54 to Restricted Substances List