GLPBio

Diethylamino hydroxybenzoyl hexyl benzoate (DHHB)

Catalog No.: GC30590Purity:>98.00%
Le diéthylamino hydroxybenzoyl hexyl benzoate (DHHB) est un absorbeur d'UV-A photostable.

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Diethylamino hydroxybenzoyl hexyl benzoate (DHHB)
Cas No.: 302776-68-7
1gIn Stock
$15.00
1
5gIn Stock
$25.00
1

Citations

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    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
  • Cell cover
    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    387(6739) (2025)
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    Science
    387(6734) (2025)
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    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    31, 1291–1307 (2021)

Description

Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) is a substituted benzophenone-type organic UV filter. Diethylamino hydroxybenzoyl hexyl benzoate absorbs UVA radiation in the 320–400nm wavelength range through its conjugated aromatic structure and converts the absorbed light energy into heat, thereby protecting the skin from photodamage. Diethylamino hydroxybenzoyl hexyl benzoate can be used in sunscreens, day creams, and other cosmetic products to provide broad-spectrum UVA protection and is applied in anti-photoaging skincare products[1-4].

In vitro, 3T3 Balb/c fibroblasts were pre-treated for 1 hour with a combination containing Diethylamino hydroxybenzoyl hexyl benzoate (62.5μg/mL), octocrylene (75μg/mL), and octyl methoxycinnamate (100μg/mL), followed by UVA radiation (5J/cm²). The combination containing Diethylamino hydroxybenzoyl hexyl benzoate did not show phototoxic potential[5]. S. cerevisiae Ogg1 mutant strain (CD138) was pre-treated with Diethylamino hydroxybenzoyl hexyl benzoate (100μg/mL) for 6 hours, followed by stimulation with solar simulated light (SSL) (2.5–10kJ/m²). Diethylamino hydroxybenzoyl hexyl benzoate increased cell survival and protected yeast cells from the toxic effects of solar simulator radiation[6].

References:
[1] Fagervold SK, Rohée C, Lebaron P. Marine sediments microbes degrade a limited repertoire of organic UV filters. Environ Sci Pollut Res Int. 2025 Jul;32(33):19823-19835.
[2] Sobańska AW, Sobański AM, Brzezińska E. Organic Sunscreens-Biological Activity from an Enzymatic Perspective. Molecules. 2026 May 14;31(10):1656.
[3] Shamoto Y, Yagi M, Oguchi-Fujiyama N, et al. Photophysical properties of hexyl diethylaminohydroxybenzoylbenzoate (Uvinul A Plus), a UV-A absorber. Photochem Photobiol Sci. 2017 Sep 13;16(9):1449-1457.
[4] Ichikawa M, Shimokawa N, Makuta M, et al. Cytotoxicity, genotoxicity, and enzyme activity effects of UV filters and their chlorinated by-products in human lung epithelial cells (A549). Sci Total Environ. 2025 Sep 24;1002:180516.
[5] Kibwila DM, Simon A, de Abreu LCL, et al. New alternatives in photoprotection: Preparation and evaluation of lamellar silicate derivatives and their use as sunscreens. Int J Cosmet Sci. 2026 Feb;48(1):172-185.
[6] Murai M, Sakurada J, Seki K, et al. Apoptosis observed in BALB/3T3 cells having ingested Staphylococcus aureus. Microbiol Immunol. 1999;43(7):653-61.

Protocole (Protocol)

Cell experiment [1]:

Cell lines

3T3 Balb/c fibroblasts (mouse fibroblast cell line)

Preparation Method

Fibroblasts were grown in two 96-well plates and preincubated with eight different concentrations of the combinations under study (C2: containing Diethylamino hydroxybenzoyl hexyl benzoate, octocrylene and octyl methoxycinnamate). After 1h incubation, one plate was subjected to 5J/cm² of UVA radiation (+UV plate) and the other was kept in a dark box (-UV plate). Cell viability was assessed by determining the uptake of neutral red dye.

Reaction Conditions

62.5μg/mL; 1h preincubation

Applications

Combinations containing Diethylamino hydroxybenzoyl hexyl benzoate did not show a phototoxic potential in the 3T3 Neutral Red Uptake Phototoxicity Test.

References:
[1] Kawakami CM, Máximo LN, Fontanezi BB, et al. Diethylamino hydroxybenzoyl hexyl benzoate (DHHB) as additive to the UV filter avobenzone in cosmetic sunscreen formulations - Evaluation of the photochemical behavior and photostabilizing effect. Eur J Pharm Sci. 2017 Mar 1;99:299-309.

Documents produit (Product Documents)

Purity:>98.00%Appearance:A solid

Propriétés chimiques (Chemical Properties)

N° CAS
302776-68-7
SMILES
O=C(OCCCCCC)C1=CC=CC=C1C(C2=CC=C(N(CC)CC)C=C2O)=O
Formule moléculaire
C24H31NO4
Masse moléculaire
397.51
Solubilité
DMSO : ≥ 50 mg/mL (125.78 mM)
Conservation
Store at -20°C, protect from light
Conseils généraux
Choisissez un solvant adapté selon les données de solubilité du produit. Après préparation, répartissez la solution mère en aliquotes afin d’éviter les cycles répétés de congélation-décongélation.
Utilisez les solutions mères dans les 6 mois si elles sont conservées à -80°C, ou dans le mois si elles sont conservées à -20°C.
Pour améliorer la solubilité, réchauffez le tube à 37°C et soniquez-le pendant une durée appropriée.
Conditions d’expédition
Les échantillons d’évaluation sont expédiés avec des blocs réfrigérants. Les autres formats sont expédiés à température ambiante ou, sur demande, avec des blocs réfrigérants.

Calculateurs (Calculators)Molarité / Dilution / Masse moléculaire / Conversion d’unités / Formulation in vivo / Solubilité

g/mol

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