原料词典检索/homosalate/HOMOSALATE
Tier 1 Monograph · SSOT 15 FieldsRaw .md (GEO) ↗
化学合成 (Synthetic)

HOMOSALATE

中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名: 胡莫柳酯 (序号 #2932)
香精 / 香料防晒剂
[EU CosIng Official Definition] Homosalate is the substituted phenolic compound that conforms to the formula:
核心法规与安全结论 (Executive Fact Box)AEO / GEO CITATION ANCHOR

化妆品中 胡莫柳酯 (HOMOSALATE) 的全球法规限值与配方应用标准是什么?

胡莫柳酯(标准 INCI: HOMOSALATE,CAS 号: 118-56-9)是化妆品配方中主要用作香精 / 香料, 防晒剂的核心成分。受中国 NMPA(限用)、韩国 MFDS(限用)及欧盟 CosIng(限用)等 6 大法域法定标准监管,常规建议添加量为 2–15%(最佳稳定窗口 pH 4–8)。

全球 7 轨官方全成分标签名称对照表

严格采用各国政府官方目录原名 · 严禁机器翻译
7-Track Official Statutory Label Names for HOMOSALATE
法域与监管轨道官方公告全成分标准名称一键复制
① 韩国 (MFDS 化妆品标准名称)HOMOSALATE (KR MFDS Registered)
② 韩国旧名称历史 (301 重定向)——
③ 欧盟 (EU CosIng EC 1223/2009)HOMOSALATE
④ 美国普通化妆品 (US PCPC / MoCRA INCI)HOMOSALATE
⑤ 美国 OTC 防晒/祛痘专论活性物名称 (FDA OTC)HOMOSALATE
⑥ 中国 (NMPA《已使用化妆品原料目录 IECIC》标准中文名)胡莫柳酯
⑦ 日本普通化妆品 / 医药部外品 (JCIA / MHLW)HOMOSALATE (标准 INCI 参照)

Layer 1 — 全球 6 大法域法定限值与监管状态

Layer 1 Statutory Regulatory Limits Across 6 Regions for HOMOSALATE
法域监管状态法定限值适用条件与法定依据来源
韩国 (MFDS)限用≤ 10%
Permitted within statutory scope
Source: ( API · [2])
欧盟 (EU)限用≤ 7.34%
Permitted within statutory scope
Source: Regulation (EC) No 1223/2009 Annex VI — via CosIng (EU Commission)
中国 (NMPA)限用≤ 10%
Permitted within statutory scope
Source: 化妆品安全技术规范(2015 Ed.) — 表5
中国 (NMPA)限用≤ 10%
Permitted within statutory scope
Source: 化妆品安全技术规范(2015年版)
美国 (FDA)限用≤ 15%
[US RESTRICTED] * 【Restrictions】 Maximum Concentration (제한) : 15% * Specific Limitations and Comments : Use of the term "sunscreen" or similar sun protection wording in a product's labeling generally causes the product to be subject to regulation as a drug or a drug/cosmetic, depending on the claims. However, sunscreen ingredients may also be used in some cosmetic products to protect the products’ color. The labelling must also state why the sunscreen ingredient is used, for example, "Contains a sunscreen to protect product color." If this explanation isn’t present, the product may be subject to regulation as a drug (21 CFR 700.35). For more information on sunscreens, refer to Tanning Products * 특별 제한조건 : "선스크린"의 단어를 사용하거나 자외선 차단과 비슷한 단어를 사용할 경우, 해당 제품은 클레임(표시광고)에 따라 제약 또는 제약/화장품의 규정을 따라야 한다. ^그러나, 자외선 차단의 성분들은 제품의 색을 보호하는 역할로 사용되기도 한다. 자외선을 차단하는 성분이 사용된 목적에 대해 라벨링에 반드시 명시해야한다. 예를 들어, "제품의 색을 보호하기 위해 자외차단제 성분을 함유하고 있다." ^만약 이러한 설명을 라벨링에 하지 않는다면, 그 상품은 제약으로서의 규정에 따라야한다. (21 CFR 700.35) ^자외선 차단에 대한 정보가 궁금하면 태닝 제품을 참고하라.
Source: API ()
韩国 (MFDS)标注要求≤ 10%
Permitted within statutory scope
Source: MFDS Functional Cosmetics Notice [Annex 4]

Layer 2 — 毒理评估与历史最高使用量 (CN IECIC / US CIR / EU SCCS)

“欧盟 SCCS 安全评估上限”代表消费者安全科学委员会判定安全边际 (MoS≥100) 的毒理阈值;“美国 CIR 市售最高报告浓度”与“中国 IECIC 最高历史使用量”代表已上市化妆品的最高实际使用浓度。

Layer 2 Toxicological & Historical Safe Use Concentrations for HOMOSALATE
安全评估依据适用范围与剂型评估浓度范围评估结论与文献档案
美国 CIR 市售最高报告浓度face_cream≤ 7.34%安全判定 (MoS≥100) ()
⚠️ 仅供参考 (免责声明): 本词典中的原料名称、法规限值与配比指南仅供研发参考。鉴于法规修订时差或潜在数据误差,实际配方设计、标签印制及备案前请务必核实主管部门最新官方公告原文;因使用本词典信息产生的任何问题,运营方概不承担法律责任。
Interactive Quartile Box-Plot (Min–Q1–Median–Q3–Max)

Layer 3 Formulation Concentration Box-Plot vs. Statutory Limit

Statutory Max: 10%
Sunscreen / Colorn=33
Min 2% · Q1 5% · Median 6% · Q3 8% · Max 15%
Sunscreen / Color — Sun care & color cosmetics dispersion / sensory modifier
Verified Source: Global Starter Formulation Library Statistical Distribution (n=33, EVONIK 18 · GRANT 9 · SEPPIC 6) (cir_safety) · EVONIK 18 · GRANT 9 · SEPPIC 6
Typical Median: 6%

Layer 3 — 剂型常规配比指南与理化配伍性

Layer 3 Formulation Concentration Quartiles by Product Category for HOMOSALATE
剂型分类Min – Q1 – Median – Q3 – Max (%)配方作用与机理Source ID
剂型组 D — 防晒霜 / 彩妆 / 粉底2% · 5% · 6% · 8% · 15%Sun care & color cosmetics dispersion / sensory modifierGlobal Starter Formulation Library Statistical Distribution (n=33, EVONIK 18 · GRANT 9 · SEPPIC 6)
Cutaneous Permeation Science (500 Dalton Rule)MW: Macro/Complex · LogP: N/A

Stratum Corneum Penetration Depth & Bio-Spicule Transdermal Delivery

Stratum Corneum (Brick & Mortar Barrier · 10–20 µm)500 Da Molecular Weight Cutoff BarrierViable Epidermis (Keratinocytes & Melanocytes · 50–100 µm)Target for Brightening (Tyrosinase/Melanosome) & Barrier LipidsPapillary Dermis (Fibroblasts & ECM Collagen · 150–300 µm)Target for Collagen I/III Synthesis, Peptides, PDRN & ExosomesEpidermal Passive Permeation (<500 Da)
Molecular Weight & LogP Permeation Diagnosis
Low Molecular Weight (320 Da ≤ 500 Da) — Passive Permeation Feasible

Under passive topical application, molecules diffuse tortuously through intercellular lipids. Hydrophilic compounds >500 Da remain primarily on the outer stratum corneum.

Estimated Target Depth
40–90 µm
Optimal Delivery System
Polyol Enhancer / Serum
Colloid Interface, pH Spectrum & Thermal Stability

pH Stability Window (0–14), Thermal Limit & HLB Colloidal Phase Behavior

Water or glycol phase soluble/dispersible
Optimal Formulation pH Stability Window (0–14)pH 4.0 – 8.0
0245.5791114

Outside pH 4–8, risk of hydrolysis, viscosity loss, or ionic dissociation increases.

Maximum Thermal Processing Limit (°C)≤ 50°C
25°C45°C60°C75°C85°C100°C

Thermally stable up to 50°C during standard emulsification.

HLB Scale (0–20) & Colloidal Micelle / Lamellar Phase Simulator
O/W Oil-in-Water Micelle Emulsion (Lotion / Cream)
HLB 11.5
W/O (3–6)Lamellar (8–10.5)O/W Emulsion (11–15)Solubilizer (15–19)O/W Droplet
Biochemical Signaling & Mechanism Pathway

Cellular & Molecular Target Mechanism Flow

1. Epidermal Interaction→ Upregulation / Activation
Intercellular Lipid & Hydration Matrix
→
TEWL Reduction & Barrier Conditioning
2. Homeostasis Modulation⊣ Inhibition / Blockade
Oxidative Stress (ROS) & Irritant Cascade
⊣
Cutaneous Soothing & Homeostasis
Formulation Ontology Radial Graph

Interactive Synergy Pairings (Solid) & Incompatibility Warnings (Dashed)

+ GLYCERIN+ CAPRYLIC/CAPRIC TR…+ TOCOPHEROL✕ Verify phase compati…HOMOSALATE
Interactive Node Guide

Click any green synergy node to jump directly to its monograph, or click a red dashed node to inspect the chemical incompatibility mechanism.

代表性商品名参考 (商标法第90条第1款第2项说明性标示)
HOMOSALATE

商品名仅供配方师识别原料规格参考,商标权归各原厂商所有。

学术与毒理综合摘要

Tier 1 Synthesis

本综述严格基于与该原料关联的 NIH PubMed 同行评审文献摘要及官方毒理学评估档案编写。

■ [1. Chemical Identity & International Labeling Nomenclature] - INCI Name: HOMOSALATE | CAS No.: 118-56-9 | EC No.: 204-260-8 - Origin: SYNTHETIC | Functions: , - Physicochemical Profile: Formula | MW /(Polymer/Complex) | / | Ionic Nature: non-ionic | CosIng/MFDS - Official Regional Label Names: US [HOMOSALATE] · EU [HOMOSALATE] · CN [胡莫柳酯] · JP [-] · JP Quasi-Drug [-] ■ [2. Dermatological Mechanism of Action & Functional Role] - Homosalate is the substituted phenolic compound that conforms to the formula: Classified under origin 'synthetic', it acts within the cosmetic vehicle or stratum corneum to deliver , performance and structural formulation stability. ■ [3. Global 6-Jurisdiction Regulatory Status & Safety Limits (Layer 1 & Layer 2)] - Regional Summary: KR: RESTRICTED | EU: RESTRICTED | US: RESTRICTED | CN: RESTRICTED | JP: NONE | ASEAN: NONE (CN IECIC (2025) Entry No. 2932 (胡莫柳酯)) - [CN / COMPOSITION / limited] (Max 10%): - [CN / COMPOSITION / limited] (Max 10%): - [KR / COMPOSITION / limited] (Max 10%): - Official Safety & Historical Use Concentration (Layer 2): sccs (reported_use, face_cream): Max 7.34% ■ [4. Formulation Dosage Guide by Product Category (Layer 3-A)] - [sun_color] Typical range: 2.0 ~ 15.0% (Median 6.0%, Ref: Global Starter Formulation Library Statistical Distribution (n=33, EVONIK 18 · GRANT 9 · SEPPIC 6)) — Sun care & color cosmetics dispersion / sensory modifier ■ [5. Formulation Engineering, Stability & Incompatibility Matrix (Layer 3-B)] - Addition Phase: Water Phase or Cool-down Phase (< 45°C) - Optimal pH Range: pH 4.0 ~ 8.0 | Max Process Temp: Max 50°C | Electrolyte Tolerance: MEDIUM - Incompatibility / Caution: Verify phase compatibility under extreme pH or high electrolyte loads - Synergy Pairings: GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL | Reference Trade Names: HOMOSALATE ■ [6. Peer-Reviewed Literature & Official Compendia Evidence] - PMID 41726609 (2026, ACS Omega): In Silico Perspective on Avobenzone, Octisalate, Octocrylene, Homosalate, and Bemotrizinol as Organic UV Filters Using D - PMID 41712751 (2026, Environ Toxicol Chem): Probabilistic emissions model for organic UV filters released to recreational waters during swimming/bathing events - PMID 41592362 (2026, Environ Int): Endogenous 15(S)-hydroxyeicosatetraenoic acid mediates amplified estrogenic responses under nanoplastic-homosalate coexp

关联同行评审文献 (NIH PubMed) (12)

In Silico Perspective on Avobenzone, Octisalate, Octocrylene, Homosalate, and Bemotrizinol as Organic UV Filters Using DFT, TD-DFT, and Molecular Dynamics [PMID: 41726609 · 2026]
Rigoni ME, de Lazaro SR, de Lara LS · ACS Omega (2026)

Ultraviolet radiation is the leading cause of skin damage, such as burns, premature aging, and the development of skin cancer. Organic sunscreens are widely used in the cosmetics industry due to their ability to absorb ultraviolet radiation and dissipate it as heat. These compounds can be susceptible to photochemical instability, which compromises their effectiveness over time and also poses environmental risks, particularly in aquatic ecosystems. This study investigated the electronic properties, absorption spectra, and solvent effects of five widely used organic UV filters: Avobenzone, Homosalate, Octisalate, Octocrylene, and Bemotrizinol. The analyses were performed through DFT and TD-DFT calculations. Solvent effects were evaluated using an implicit solvent model and complemented by molecular dynamics simulations in an aqueous environment.

Probabilistic emissions model for organic UV filters released to recreational waters during swimming/bathing events [PMID: 41712751 · 2026]
Federle TW, Fleming ML, Davies IA, Versteeg DJ · Environ Toxicol Chem (2026)

A critical element for understanding measured concentrations and predicting exposure levels of UV filters (UVFs) in recreational waters relates to mass released from sunscreen products applied to skin during swimming and bathing. A probabilistic mass transfer kinetic model was developed to estimate distributions of the mass of five organic UVFs released during individual swim events with sunscreen. The model incorporates the ratios of different demographics and distributions of their total skin areas, adjusted to account for body areas to which sunscreens are not typically applied or do not contact water. The resulting distribution of skin areas is combined with distributions of sunscreen application rates and UVF levels in sunscreen products to generate a distribution of UVF masses on skin that are exposed to water with the fraction released to water calculated using a first-order equation describing the kinetics of release. The predicted median mass released during a swim event was 112&#x2009;mg for oxybenzone, 32.6&#x2009;mg for avobenzone, 23.5&#x2009;mg for octocrylene, 47.7&#x2009;mg for homosalate, and 7.59&#x2009;mg for octisalate. As proof of principle, the model was used to repeat previous modeling at Proph&#xe8;te Beach, which resulted in predicted median values for oxybenzone and avobenzone within a factor of three of the reported measured environmental concentrations.

Endogenous 15(S)-hydroxyeicosatetraenoic acid mediates amplified estrogenic responses under nanoplastic-homosalate coexposure [PMID: 41592362 · 2026]
Li Z, Chen X, Yang X, Huang X, Ye R, Du J, Tang S, Qiu A, Huang Y, Deng Y, Zhong Y, Liang B, Hui CY, Chen D, Huang Z · Environ Int (2026)

Micro- and nanoplastics (MNPs) can enhance the toxicity of co-occurring chemicals via a proposed "Trojan horse" effect, yet the underlying mechanisms remain unclear. Here, we investigated the estrogenic effects of coexposure of ultraviolet filter homosalate (HMS) and polystyrene nanosphere (PNS) using ovariectomized mice (HMS: 0.1 and 1&#xa0;mg/kg; PNS: 2.5&#xa0;mg/kg) and human cell models (HMS: 0.01&#xa0;-&#xa0;1&#xa0;&#x3bc;M; PNS: 1 mg/L). In mice, HMS-PNS coexposure significantly increased uterine weight, promoted mammary gland proliferation, and upregulated estrogen receptor 1 and its downstream targets amphiregulin and progesterone receptor. Integrated metabolomic and transcriptomic analyses identified endogenous 15(S)-hydroxyeicosatetraenoic acid (15(S)-HETE) as a key mediator of these effects in mammary glands. In MCF-7 cells, HMS-PNS coexposure elevated 15(S)-HETE levels, promoting cell proliferation via the estrogen receptor alpha-arachidonate 15-lipoxygenase (ER&#x3b1;-ALOX15) axis. At a concentration of 100&#xa0;nM 15(S)-HETE, pharmacological inhibition of phosphoinositide 3-kinase/protein kinase B (PI3K/AKT) abrogated cell proliferation and serum and glucocorticoid-regulated kinase 1 (SGK1) activation. Moreover, immunoprecipitation and docking analyses suggested a direct interaction between 15(S)-HETE and SGK1. Knockdown of ALOX15, or PI3K/AKT inhibition, suppressed HMS-PNS-induced cell proliferation. Taken together, these results demonstrated that HMS-PNS coexposure amplifies estrogenic responses through ER&#x3b1;-ALOX15-dependent 15(S)-HETE production and PI3K/AKT/SGK1 signaling. Our findings uncover a mechanistic pathway beyond the canonical "Trojan horse" effect, providing new insight into how MNPs modulate endocrine-disrupting activity of co-occurring contaminants and informing future risk assessment of combined environmental exposures.

Pyroptosis- and Necroptosis-Related Signaling in Salicylate UV Absorber-Induced Toxicity: Implications for Sustainable Chemistry and Human Health [PMID: 42278310 · 2026]
He C, Wang Y, Lin J, et al. · Int J Mol Sci (2026)

As emerging global environmental contaminants, organic ultraviolet absorbers (OUVAs) are widely used in personal care formulations and exhibit environmental persistence and potential bioaccumulation. Among these compounds, 2-ethylhexyl salicylate (EHS) and homosalate (HMS) are the most frequently used salicylate-type UV filters in cosmetic formulations. Although an increasing number of studies have demonstrated their environmental hazards, little is known about the molecular mechanisms underlying their cytotoxicity in mammalian systems, a fundamental knowledge gap for both human health protection and the development of more environmentally friendly consumer goods. In this study, we used mouse embryonic fibroblasts (MEFs, 3T6) and zebrafish as models to assess the toxicological phenotypes of EHS and HMS in vitro and in vivo, respectively. We found that both EHS and HMS induced cellular damage characterized by oxidative stress, disrupted intracellular calcium homeostasis, mitochondrial impairment, and DNA damage. Importantly, molecular analyses further suggested the concurrent activation of two distinct regulated cell death programs: pyroptosis, as suggested by Caspase-11 -mediated GSDMD cleavage, and necroptosis, as suggested by ZBP1-RIPK3-Caspase-8 -mediated MLKL phosphorylation. The in vitro data have been partially validated at the level of gene expression and in developmental toxicity in the zebrafish model, providing some in vivo phenotypic and molecular correlates. While the upstream events were experimentally verified, the causal links among them remain to be further elucidated. Taken together, this work suggested that OUVA-induced toxicity is not limited to isolated oxidative damage, but may also involve the activation of two different cell death programs. These findings provide important molecular clues to understanding the potential health and ecological risks of widely used UV filters and offer a scientific basis for their more environmentally friendly safety evaluation and regulatory management, which are crucial for advancing more sustainable chemistry and safer consumer goods.

Laser-induced hyperspectral fluorescence for spatio-chemical detection of sunscreen contaminants in food-grade sea salt using sparse PCA-SVM analysis [PMID: 42084616 · 2026]
Ebrahem M, Hosni MI, Abdallah A, et al. · Environ Geochem Health (2026)

Sea salt increasingly harbors organic contaminants from personal care products, yet current monitoring methods lack spatial resolution and require destructive sampling. This study introduces an innovative analytical framework integrating Laser-Induced Fluorescence (LIF) Hyperspectral Imaging (HSI) with machine learning for the rapid, non-destructive detection of sunscreen residues on salt crystals. To simulate contamination, seawater from the Mediterranean coast (Alexandria, Egypt) was spiked to achieve a 10&#xa0;mg/L sunscreen concentration within the seawater matrix prior to crystallization; this formulation contained Ethylhexyl Methoxycinnamate, Homosalate, and Ethylhexyl Salicylate. A SOC710 HS camera (128 bands) acquired fluorescence data under 450&#xa0;nm laser excitation. Raw data underwent preprocessing and dimensionality reduction via Sparse Principal Component Analysis (Sparse PCA, &#x3bb;&#x2009;=&#x2009;0.5, k&#x2009;=&#x2009;4 components, 73.4% sparsity). A Support Vector Machine (SVM) with an RBF kernel was trained on these sparse features. Performance evaluation employed tenfold stratified cross-validation, an 80-20 holdout test on ROI-based spectra, and independent sample validation against manually annotated pixel-wise ground-truth masks. While ROI-based tests yielded near-perfect accuracy under ideal conditions, full-image evaluation achieved &#x2248;96% pixel-wise accuracy (precision&#x2009;&#x2248;&#x2009;0.99, recall&#x2009;&#x2248;&#x2009;0.95, F1&#x2009;&#x2248;&#x2009;0.97), providing a realistic estimate under heterogeneous conditions. Full-image classification mapped widespread contamination (57.8% of pixels), whereas an independently prepared clean salt sample produced zero false positives. The integrated Sparse PCA-SVM framework transforms fluorescence-imaging data into spatio-chemical maps, simultaneously revealing contaminant presence and spatial distribution on salt surfaces, thereby offering a powerful paradigm for the interpretable monitoring of organic pollutants in food materials.

Pending Food and Drug Administration approval of bemotrizinol: A potential turning point for United States sunscreen formulation [PMID: 42067042 · 2026]
Wang SQ, Osterwalder U, Lim HW · J Am Acad Dermatol (2026)
Sunscreens [PMID: 41730063 · 2006]
Unknown Authors · PubMed Journal (2006)
Development and preliminary validation of an analytical methodology for the determination of organic UV filters in zooplankton samples [PMID: 41544515 · 2026]
Íñiguez E, Gouazé M, Dinis A, et al. · Mar Pollut Bull (2026)

The release of chemicals into marine environments from coastal human activities has raised growing concern about pollution. Among these chemicals, organic ultraviolet filters (oUVFs), widely used in personal care products and industrial applications, have recently been identified as pollutants of emerging concern. Their extensive use and persistence highlight the need to assess their occurrence and potential impacts on aquatic ecosystems. This study aimed to optimize and apply an analytical methodology for the determination of eleven oUVFs in zooplankton matrices. Microwave-assisted extraction (MAE) was employed for sample preparation, while ultra-high-performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS) enabled the identification and quantification of the target compounds. Extraction parameters, including solvent, temperature, and time, were systematically optimized to enhance recovery and ensure accuracy and precision in complex biological samples. The method achieved limits of detection (MLOD) between 1.47 and 5.98&#xa0;ng&#xa0;g -1 dry weight (d.w.) and method limits of quantification (MLOQ) between 4.900 and 19.92&#xa0;ng&#xa0;g -1 d.w. Recovery efficiencies were low, ranging from 28 to 63&#xa0;%, reflecting the diverse physicochemical properties of oUVFs and the strong matrix effects associated with zooplankton heterogeneity. Application of the validated method to zooplankton collected around Madeira Island (Portugal) revealed the presence of six oUVFs. Homosalate was the most frequently detected compound (53&#xa0;% of samples), while octocrylene exhibited the highest concentrations, ranging from 24.01 to 1029&#xa0;ng&#xa0;g -1 d.w. These findings demonstrate the relevance of zooplankton as bioindicators of oUVF contamination and support the need for regulatory monitoring and ecological risk assessments in coastal ecosystems.

Occurrence of twelve UV filters and evidence of cis-octinoxate formation in Adriatic coastal waters: Environmental implications [PMID: 41518963 · 2026]
Zulfiqar H, Llompart M, Castiñeira-Landeira A, et al. · Mar Pollut Bull (2026)

UV filters used in personal care products are increasingly recognised as emerging contaminants due to their persistence and ecological risks. Detected in aquatic systems at concentrations from ng&#xa0;L -1 to &#x3bc;g&#xa0;L -1 , their monitoring is essential for environmental risk assessment but challenging because of their diverse physicochemical properties, requiring sensitive analytical methods. This study optimised a solid-phase extraction gas chromatography-tandem mass spectrometry (SPE-GC-MS/MS) method for the simultaneous determination of twelve UV filters in marine waters. The method showed suitable linearity, precision, and recoveries, with detection limits below 1&#xa0;ng&#xa0;L -1 . Seawater samples collected along the Adriatic coast (Rimini and Riccione, Italy) during peak recreational activity were analysed. All twelve UV filters were detected, with octocrylene (up to 23,100&#xa0;ng&#xa0;L -1 ), homosalate (up to 16,400&#xa0;ng&#xa0;L -1 ), and ethylhexyl salicylate (up to 10,900&#xa0;ng&#xa0;L -1 ) being most abundant. Trans-2-Ethylhexyl methoxycinnamate (E-EHMC, the trans isomer of octinoxate, 13-1474&#xa0;ng&#xa0;L -1 ) occurred consistently with its isomer Z-EHMC (cis-octinoxate), contributing 18-64&#xa0;% of total (E&#xa0;+&#xa0;Z)-EHMC, suggesting in situ photochemical conversion, since the cis form is negligible in cosmetic products. Benzophenone, ethylhexyl dimethyl PABA, 4-methylbenzylidene camphor, benzyl salicylate, and isoamyl methoxycinnamate were found at lower yet relevant concentrations. UV filters banned under European regulations, such as menthyl anthranilate and etocrylene, were absent or barely detected. This work provides the first data on sunscreen UV filters in Adriatic coastal waters and the first quantitative evidence of Z-EHMC in environmental waters, highlighting its in situ formation and contributing to understanding their environmental fate and risks.

Assessing the hepatic metabolism of six sunscreen ultraviolet filters: In vitro-in vivo extrapolation approach using human liver microsomes and hepatic parameter predictions for exposure risk assessment [PMID: 41319926 · 2026]
Baviera GS, Poli VR, Oka-Duarte L, et al. · Biochem Pharmacol (2026)

The present work investigates the in vitro hepatic metabolism of six commonly used sunscreen UV filters: oxybenzone, avobenzone, octocrylene, octinoxate, octisalate, and homosalate, using human liver microsomes. In vitro-in vivo extrapolation was performed to predict key metabolic parameters, including hepatic clearance (CL H ) and hepatic extraction ratio (E H ), providing valuable insights into the potential systemic persistence of these compounds after dermal or oral absorption. Additionally, reaction phenotyping was conducted for the first time to characterize the human liver enzymes involved in the metabolism of these sunscreen UV filters, with carboxylesterases (CES) playing a key role in the biotransformation of ester-containing compounds such as octocrylene and octinoxate. Furthermore, oxybenzone is predominantly metabolized by CYP2C19 and CYP1A2, while avobenzone is primarily metabolized by CYP2C19, CYP2C9, and CYP1A2. The results showed significant variability in metabolic stability and systemic clearance, with compounds like octocrylene exhibiting relatively higher half-lives, suggesting potential for bioaccumulation. The findings highlight the importance of understanding the kinetic profiles of sunscreen UV filters for more accurate risk assessments, particularly in the context of prolonged human exposure.

Green-synthesized Tio₂ Nanoparticles for Sunscreen: Eco-Friendly Approach to Spf Enhancement [PMID: 41236699 · 2026]
Murugesan P, Kamalakannan S, Thangarathinam K, et al. · Appl Biochem Biotechnol (2026)

This study aims to evaluate the potential of green-synthesized titanium dioxide (TiO&#x2082;) nanoparticles (NPs) derived from herbal extracts-namely Camellia sinensis (Green Tea), Eclipta prostrata (Bhringraj), Glycyrrhiza glabra (Licorice), and Cinnamomum zeylanicum (Cinnamon)-for enhancing the Sun Protection Factor (SPF) in sunscreen formulations. Addressing the environmental and toxicity concerns associated with conventionally synthesized TiO&#x2082; NPs, this eco-friendly approach offers a sustainable and effective alternative for cosmetic applications without compromising efficacy. The synthesized nanoparticles were characterized using UV-Vis spectroscopy, X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR), and then incorporated into oil-in-water emulsions containing 5% homosalate. In vitro SPF was measured using the Labsphere UV-2000S system, while formulation stability was assessed via pH monitoring, rheological behavior, and accelerated centrifugation using the LUMiSizer. Statistical analysis, including one-way ANOVA and effect size metrics (&#x3b7; 2 , Cohen's d), confirmed significant SPF enhancement, particularly in formulations using Green Tea and Cinnamon-derived TiO&#x2082; NPs, which showed 3.12-fold and 3.11-fold improvements, respectively. Notably, smaller crystallite size (30.2&#xa0;nm in Green Tea-derived TiO&#x2082;) correlated with higher SPF (14.97&#x2009;&#xb1;&#x2009;0.31). All formulations exhibited excellent physical and thermal stability. These findings underscore the promise of plant-mediated TiO&#x2082; NPs as a viable, sustainable solution for next-generation sunscreen products, with further investigation warranted for scale-up and in vivo validation.

Nationwide occurrence of emerging benzophenone, benzotriazole, salicylate and triazine ultraviolet filters in coastal sediment of China: Spatial distribution, source and ecological risk [PMID: 41101667 · 2025]
Tang Z, Wu Z, Jia X, et al. · Environ Res (2025)

Ultraviolet filters (UVFs), widely used in industrial and personal care products, are emerging environmental contaminants of great concern because of their persistence, bioaccumulation and toxicity. Sediments are generally considered the reservoir and secondary source of UVFs, yet knowledge of the occurrence of these emerging contaminants in coastal sediments on a large geographical scale remains unknown. In this study, 31 out of 37 target UVFs were detected in 91 sediment samples collected from 43 coastal cities of China. Benzophenone UVFs exhibited the highest mean total concentration of 5374.8&#xa0;pg/g, followed by benzotriazole (3298.3&#xa0;pg/g), salicylate (3094.1&#xa0;pg/g) and triazin UVFs (61.2&#xa0;pg/g), respectively. Spatial analysis revealed significantly higher UVF concentrations ranging from 1839&#xa0;pg/g to 82,308&#xa0;pg/g in coastal sediments from the Yellow Sea compared with those of the South China Sea, the East China Sea and the Bohai Sea (p&#xa0;&lt;&#xa0;0.05). Source apportionment indicated that the emissions from industrial productions, cosmetics and personal care products are major contributors to UVF contamination. A nationwide mass inventory identified the Liaodong Peninsula, Yangtze River Estuary, Pearl River Estuary, and north-east Hainan Province as UVF accumulation hotspots, influenced by tourism, industrial activities, and ocean currents. Ecological risk assessment showed that seven UVFs, including Benzophenone-7 (BP-7), 2-(benzotriazol-2-yl)-4-tert-butylphenol (UV-PS), 2-tert-butyl-6-(5-chlorobenzotriazol-2-yl)-4-methylphenol (UV-326), 2,4-ditert-butyl-6-(5-chlorobenzotriazol-2-yl) phenol (UV-327), 2-(benzotriazol-2-yl)-4-(2,4,4-trimethylpentan-2-yl) phenol (UV-329), 2-Ethylhexyl salicylate (EHS) and Homosalate (HMS), posed significant ecological risks (RQ&#xa0;&gt;&#xa0;0.1) in coastal sediments. This work delivers the first nationwide assessment of four classes of UVFs contamination in coastal sediments of China, providing critical data for their environmental mitigation and management.

常见问题解答 (FAQ)

Q1. 胡莫柳酯 (HOMOSALATE) 在全球 7 大法域的官方全成分标签名称是什么?
中国 NMPA《已使用化妆品原料目录 (IECIC)》标准中文名为 '胡莫柳酯',美国 PCPC 与欧盟 CosIng 标准 INCI 为 'HOMOSALATE',日本 JCIA 表示名称为 'HOMOSALATE'。
Q2. 胡莫柳酯 (HOMOSALATE) 在中、韩、欧、美、日、东盟的法定监管状态 (Layer 1) 如何?
6 大法域监管汇总 — 中国(CN): restricted,韩国(KR): restricted,欧盟(EU): restricted,美国(US): restricted,日本(JP): none,东盟(ASEAN): none。
Q3. 胡莫柳酯 (HOMOSALATE) 的常规配方添加量 (Layer 3) 与最佳稳定 pH 窗口是多少?
在代表性剂型 (sun_color) 中常规添加量为 2%–15%(中位数 6%),最佳稳定 pH 范围为 4–8。
Q4. 胡莫柳酯 (HOMOSALATE) 有哪些配伍禁忌 (Incompatibilities) 与协同增效组合?
推荐协同组合包括 GLYCERIN, CAPRYLIC/CAPRIC TRIGLYCERIDE, TOCOPHEROL;配伍禁忌注意:Verify phase compatibility under extreme pH or high electrolyte loads。