Determine the necessary mass, volume, or concentration for preparing a solution.
Type NP-4 for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships FedEx DG Service 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 5 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Tergitol is a non-ionic surfactant. Non ionic surfactants used in paint and coatings, paper and textile processing, cleaning agents and detergents, agricultural chemicals, and metalworking fluids; It has excellent descaling properties, outstanding wettability, universal solubility, and excellent processing performance. It can also be used for oilfield drilling and production formulation.
Benefits
· Excellent oil-soluble surfactant
· Low HLB emulsifier
· Low odor
· Exceptional handling properties
Application
Tergitol has been used in a study to evaluate the structural characteristics and antibacterial properties of silver nanoparticles. In a study, it was also used to investigate the detection of Salmonella serotype enteritis in the gut from environmental samples of natural pollution in a comprehensive poultry house. Can be used for: cleaning product formulations, paints and coatings, emulsion polymerization, and any place where surface activity needs to be increased.
Advantage
Combining economy and high performance;
Excellent descaling and wetting properties;
Good solubility and emulsification.
Typical Properties | |
|---|---|
| % Actives | 100 % |
| Chemistry | Alkylphenol Ethoxylate (APE) |
| Cloud Point @1% Aqueous (ASTM D 2024) | Insoluble °C |
| CMC (25°C) | Insoluble PPM |
| Foam Height - Initial (0.1 wt% actives) | Insoluble mm |
| Form | Liquid |
| HLB | 8.9 |
| Moles EO | 4 |
| Pour Point | -28 °C |
| Use | Scouring |
| Canonical Smiles | CCCCCCCCCC1=CC=C(C=C1)OCCO |
|---|---|
| IUPAC Name | 2-(4-nonylphenoxy)ethanol |
| InChIKey | KUXGUCNZFCVULO-UHFFFAOYSA-N |
| INCHI | 1S/C17H28O2/c1-2-3-4-5-6-7-8-9-16-10-12-17(13-11-16)19-15-14-18/h10-13,18H,2-9,14-15H2,1H3 |
| Isomeric SMILES | CCCCCCCCCC1=CC=C(C=C1)OCCO |
| WGK Germany | 2 |
| UN Number | 3082 |
| Packing Group | III |
| Reaxy-Rn | 2111973 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2111973&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 |
| Class | Phenol ethers |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenol ethers |
| Alternative Parents | Phenoxy compounds Alkyl aryl ethers Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Apr 22, 2025 | T767863 | |
| Certificate of Analysis | Apr 22, 2025 | T767863 | |
| Certificate of Analysis | Apr 22, 2025 | T767863 | |
| Certificate of Analysis | Apr 22, 2025 | T767863 | |
| Certificate of Analysis | Apr 22, 2025 | T767863 |
| Solubility | · Insoluble in water · Soluble in chlorinated solvents and most polar and non-polar solvents and oils · Chemically stable in the presence of dilute acids, bases and salts · Compatible with soaps, anionic and other nonionic surfactants, and many organic |
|---|
| 1. Hu Jun, Shi Lei-ting, Luo Yue, Chen Mao, Jin Cheng, Guo Yong-jun, Yuan Na. (2025) A surfactant-polymer and macromolecular surfactant compound system for enhancing heavy oil recovery: Synthesis, characterization and mechanism. COLLOID AND POLYMER SCIENCE, [PMID:] [10.1007/s00396-025-05373-z] |
| 2. Xiangrui Chen, Zhiming Liu, Zhen Pan, Liyan Shang, Yuchuan Qian, Houxue Song. (2025) Experimental Study on the Growth of Methane Hydrate by Amino Acid Solution in the Oil–Water System. LANGMUIR, [PMID:40911725] [10.1021/acs.langmuir.5c02757] |
| 3. Shengzong Lan, Liuyang Dong, Peilun Shen, Qifang Zheng, Lidong Qiao, Dianwen Liu. (2024) Synergistic impact of surfactant and sodium oleate on dolomite removal from fluorapatite via reverse flotation. APPLIED SURFACE SCIENCE, [PMID:] [10.1016/j.apsusc.2024.159504] |
| 4. Zhaohua Wang, Sayma Sathi, Xiaofeng Niu, Qikang Tian, Gang Zhang, Jinming Zhao. (2025) Humidity and temperature control performance of metal organic frameworks and microencapsulated PCMs composite material. CONSTRUCTION AND BUILDING MATERIALS, [PMID:] [10.1016/j.conbuildmat.2025.142186] |
| 5. Xuezhi Li, Bin Ma, Liming Fu, Jing Bai, Qingbing Zhang, Baolu Yu. (2025) Synthesis and Mechanistic Study of a Copolymer Demulsifier for Dehydration of Water-in-Oil Emulsion of Crude Oil. ChemistryOpen, [PMID:40557520] [10.1002/open.202500188] |