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Common Name(s): Neohesperidin,neohesperidin,bitter orange flavanone glycoside,sweetness modifier anti-inflammatory active

CAS Number: N/a

DESCRIPTION

What It Does: Provides bitter taste masking for oral care and edible cosmetics through t2r receptor competitive antagonism, anti-inflammatory cox-1/2 and 5-lox inhibition from the flavanone catechol, and antioxidant radical scavenging.

Why It's Used: Neohesperidin's rutinose (neohesperidoside) linkage is specifically recognised by t2r bitter receptors as a partial agonist that blocks full agonist access โ€” providing bitter masking at concentrations below the receptor saturation threshold.

How It Works: Neohesperidin t2r competitive antagonism: neohesperidoside sugar geometry fits the t2r38/t2r14 bitter receptor binding site as partial agonist โ†’ blocks full agonist (caffeine, quinine, isohumulones) access โ†’ bitter taste reduction. flavanone chromophore: cox-1/2 competitive inhibition (ic50 ~15 ฮผm); catechol b-ring radical h-atom donation.

Typically Found In: Oral care,anti-inflammatory,bitter masking

TECHNICAL DETAILS

Primary Category: Active ingredient โ€“ antioxidant

Secondary Functions: Free radical scavenging,anti-aging

Application Areas:

Facial Skincare

Body Care

Hair Care

Beard Care

Color Cosmetics (Makeup)

Dietary/Oral Supplements

Typical Concentration Range: 0.01%โ€“2%

SOURCING & ETHICS

Vegan Status: Yes

Halal Status: Yes

Source Notes: Plant-derived extract or synthetic.

SKIN COMPATIBILITY

Irritancy Rating: 1/5 โ€“ very low

Comedogenicity Rating: 0/5 โ€“ non-comedogenic

Sensitivity Concerns: Non-irritating; well-tolerated.

Safe for Sensitive Skin: Yes

SAFETY & COMPATIBILITY

Safety Profile: Excellent safety profile. ewg score: 1.

Works Well With: Vitamin c,vitamin e,ferulic acid,spf,other antioxidants

Avoid Combining With: No significant incompatibilities

SCIENTIFIC NOTE

Neohesperidin vs naringenin: both flavanones provide anti-inflammatory activity but neohesperidin's neohesperidoside linkage provides the bitter-masking activity absent in naringenin's glucoside form โ€” the specific sugar linkage geometry determines the t2r receptor interaction.

Last Verified: 2026-03-22

Primary Sources: Cosing database,neohesperidin bitter masking anti-inflammatory review