≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 16 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis.
Usually used in a rapid staining method for identification of macrophages; counts by this method were confirmed by the more complex morphological criteria, by phagocytosis, and by the presence of Fc receptors.
product description：
1-Naphthyl acetate is a 1-napthyl ester. Mechanism of photo-Fries rearrangement of 1-naphthyl acetate has been studied using steady state photolysis and laser flash photolysis. Kinetics of photo-Fries rearrangement of 1-napthyl acetate has been studied using steady-state, time-resolved chemically induced dynamic nuclear polarization (CIDNP) and flash photolysis methods.
| Sonrisas canónicas | CC(=O)OC1=CC=CC2=CC=CC=C21 |
|---|---|
| IUPAC Name | naphthalen-1-yl acetate |
| InChIKey | VGKONPUVOVVNSU-UHFFFAOYSA-N |
| INCHI | 1S/C12H10O2/c1-9(13)14-12-8-4-6-10-5-2-3-7-11(10)12/h2-8H,1H3 |
| Isómeros SMILES | CC(=O)OC1=CC=CC2=CC=CC=C21 |
| WGK Alemania | 3 |
| Peso molecular | 186.21 |
| Beilstein | 2046403 |
| Reaxy-Rn | 2046403 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2046403&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Clase | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Carboxylic acid esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homopolycyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
| External Descriptors | a small molecule |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 C2321587 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| C2321632 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| C2321687 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| C2321689 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| C2321690 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| C2321692 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| D2521663 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| E2628069 | Certificate of Analysis | Mar 08, 2023 | N110629 |
| Solubilidad | Soluble in ethanol. |
|---|---|
| Sensibilidad | Moisture sensitive. |
| Punto de inflamación (°F) | >110℃ |
| Punto de inflamación (°C) | >110℃ |
| Punto de ebullición (°C) | 118°C |
| Punto de fusión (°C) | 49°C |
| Peso molecular | 186.210 g/mol |
| XLogP3 | 2.800 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 186.068 Da |
| Monoisotopic Mass | 186.068 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 212.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Liu Lang, Wang Suji, Zuo Junfeng, Zhang Xiaohe, Peng Xiong, Wang Kang, Chen Maohua. (2023) Characterization and fitness cost of bifenthrin resistance in Rhopalosiphum padi (Hemiptera: Aphididae). JOURNAL OF ECONOMIC ENTOMOLOGY, [PMID:37478406] [10.1093/jee/toad143] |
| 2. Xueqing Yang, Xinru Li, Xinzhu Cang, Jianglong Guo, Xiujing Shen, Kongming Wu. (2021) Influence of seasonal migration on the development of the insecticide resistance of oriental armyworm (Mythimna separata) to λ-cyhalothrin. PEST MANAGEMENT SCIENCE, 78 (3): (1194-1205). [PMID:34825453] [10.1002/ps.6736] |
| 3. Yifan Li, Hong Sun, Zhen Tian, Yue Li, Xuan Ye, Ruichi Li, Xinyu Li, Shengli Zheng, Jiyuan Liu, Yalin Zhang. (2020) Identification of key residues of carboxylesterase PxEst-6 involved in pyrethroid metabolism in Plutella xylostella (L.). JOURNAL OF HAZARDOUS MATERIALS, [PMID:33338816] [10.1016/j.jhazmat.2020.124612] |
| 4. Zi-Guo Wang, Shan-Shan Jiang, David Mota-Sanchez, Wei Wang, Xin-Ru Li, Yu-Lin Gao, Xu-Peng Lu, Xue-Qing Yang. (2019) Cytochrome P450-Mediated λ-Cyhalothrin-Resistance in a Field Strain of Helicoverpa armigera from Northeast China. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:30882220] [10.1021/acs.jafc.8b07308] |
| 5. Li-sha Bai, Cai-xia Zhao, Jing-jing Xu, Chuan Feng, Yong-qiang Li, Yan-ling Dong, Zhi-qing Ma. (2019) Identification and biochemical characterization of carboxylesterase 001G associated with insecticide detoxification in Helicoverpa armigera. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, [PMID:31153479] [10.1016/j.pestbp.2019.03.009] |
| 6. Lu Xu, Jun Zhao, Yang Sun, Dejin Xu, Guangchun Xu, Xiaolong Xu, Yueliang Zhang, Shuijin Huang, Zhaojun Han, Zhongyan Gu. (2018) Constitutive overexpression of cytochrome P450 monooxygenase genes contributes to chlorantraniliprole resistance in Chilo suppressalis (Walker). PEST MANAGEMENT SCIENCE, 75 (3): (718-725). [PMID:30101471] [10.1002/ps.5171] |
| 7. Yunhe Zhao, Shuangyu Xu, Hongbao Lu, Daxia Zhang, Feng Liu, Jin Lin, Chenggang Zhou, Wei Mu. (2017) Effects of the plant volatile trans‑2-hexenal on the dispersal ability, nutrient metabolism and enzymatic activities of Bursaphelenchus xylophilus. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, [PMID:29183585] [10.1016/j.pestbp.2017.08.004] |
| 8. Yongqiang Li, Jianwei Liu, Mei Lu, Zhiqing Ma, Chongling Cai, Yonghong Wang, Xing Zhang. (2016) Bacterial Expression and Kinetic Analysis of Carboxylesterase 001D from Helicoverpa armigera. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 17 (4): (493). [PMID:27049381] [10.3390/ijms17040493] |
| 9. Xingyue Luo, Chun Ji, Xiao Wang, Laping He, Yuangen Wu, Han Tao. (2025) A plant esterase-catalyzed electrochemical sensing strategy for organophosphorus pesticide using 2,6-dichlorophenolindophenol as signal probe and FeSAC-NPC as electrocatalyst. MICROCHEMICAL JOURNAL, [PMID:] [10.1016/j.microc.2025.113129] |
| 10. Yongmei Chang, Weihuan Xu, Shan Wang, Mengyao Zhu, Yanan Ru, Zhiheng Xu, Guangyou Chen, Yongqiang Li. (2024) Characterization of Four Carboxylesterases Involved in Detoxification of β-Cypermethrin, λ-Cyhalothrin, and Malathion in Helicoverpa armigera. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:39508741] [10.1021/acs.jafc.4c07451] |
| 11. Donglin Xiang, Shuyi Qiu, Laping He, Chun Ji, Jiayu Chen, Yuangen Wu, Han Tao. (2024) Purification, characterization of a plant esterase from red kidney bean and its feasibility for pesticide residue analysis in foods. Food Bioscience, [PMID:] [10.1016/j.fbio.2024.103944] |
| 12. Shuqi Xing, Wei Xie, Guangli Hu, Chaocheng Luo, Hong Zhu, Laping He, Cuiqin Li, Xiao Wang, Xuefeng Zeng. (2024) The synthesis of cinnamyl acetate and deacetyl-7-aminocephalosporanic acid by a GDSL-type esterase and its substrate specificity analysis. ENZYME AND MICROBIAL TECHNOLOGY, [PMID:39471645] [10.1016/j.enzmictec.2024.110532] |
| 13. Xiaodan Yan, Jianjun Wang, Yu Sun, Junge Zhu, Sheng Wu. (2016) Facilitating the Evolution of Esterase Activity from a Promiscuous Enzyme (Mhg) with Catalytic Functions of Amide Hydrolysis and Carboxylic Acid Perhydrolysis by Engineering the Substrate Entrance Tunnel. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 82 (22): [PMID:27613682] [10.1128/AEM.01817-16] |
| 14. Hong-xue Qi, Hui-zhen Li, Ping Ma, Jing You. (2015) Integrated sediment quality assessment through biomarker responses and bioavailability measurements: Application in Tai Lake, China. ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, [PMID:26004354] [10.1016/j.ecoenv.2015.05.007] |
| 15. Yunfei Zhang, Xinyi Hu, Junjie Yin, Jiabin Chen, Shujing Zhang, Fang Wang. (2025) Association of VGSC Mutations and P450 Overexpression with Beta-Cypermethrin Resistance in Aphis gossypii Glover from a Chinese Wolfberry (Lycium barbarum L.) Field. Agriculture-Basel, 16 (1): (83). [PMID:] [10.3390/agriculture16010083] |
| 16. Longying Zhao, Jiayu Chen, Donglin Xiang, Mierban Dawuti, Laping He, Yuangen Wu, Han Tao. (2026) Electrochemical Sensing of Organophosphorus Pesticides Based on Plant Esterase-Triggered Silver Deposition with CuNi-DAC Signal Amplification. ELECTROCHIMICA ACTA, [PMID:] [10.1016/j.electacta.2026.148562] |
