Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
pharmaceutical grade, PharmPure™ Pharmaceutical grade,PharmPure™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,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 18 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | CCOC(=O)CC(CC(=O)OCC)(C(=O)OCC)O |
|---|---|
| IUPAC Name | triethyl 2-hydroxypropane-1,2,3-tricarboxylate |
| InChIKey | DOOTYTYQINUNNV-UHFFFAOYSA-N |
| INCHI | 1S/C12H20O7/c1-4-17-9(13)7-12(16,11(15)19-6-3)8-10(14)18-5-2/h16H,4-8H2,1-3H3 |
| Isomeric SMILES | CCOC(=O)CC(CC(=O)OCC)(C(=O)OCC)O |
| WGK Germany | 3 |
| RTECS | YO8400000 |
| PubChem CID | 6506 |
| UN Number | 1299 |
| Packing Group | III |
| Molecular Weight | 136.23 |
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 | Organic acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Tricarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tricarboxylic acids and derivatives |
| Alternative Parents | Fatty acid esters Tertiary alcohols Carboxylic acid esters Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Tricarboxylic acid or derivatives - Fatty acid ester - Fatty acyl - Tertiary alcohol - Carboxylic acid ester - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. |
| External Descriptors | Not available |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 13, 2026 | T111672 | |
| Certificate of Analysis | Sep 16, 2025 | T111672 | |
| Certificate of Analysis | Jul 25, 2025 | T111672 | |
| Certificate of Analysis | Feb 27, 2025 | T111672 | |
| Certificate of Analysis | Nov 30, 2024 | T111672 | |
| Certificate of Analysis | Nov 30, 2024 | T111672 |
| Sensitivity | Light sensitive. |
|---|---|
| Refractive Index | 1.4680-1.4780 |
| Boil Point(°C) | 154-170°C |
| Melt Point(°C) | -55°C |
| Molecular Weight | 276.280 g/mol |
| XLogP3 | 0.100 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 11 |
| Exact Mass | 276.121 Da |
| Monoisotopic Mass | 276.121 Da |
| Topological Polar Surface Area | 99.100 Ų |
| Heavy Atom Count | 19 |
| Formal Charge | 0 |
| Complexity | 304.000 |
| 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 |
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| 3. Bin Liu, Danyang Fu, Hang Ning, Ming Tang, Hui Chen. (2022) Knockdown of CYP6CR2 and CYP6DE5 reduces tolerance to host plant allelochemicals in the Chinese white pine beetle Dendroctonus armandi. PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY, [PMID:36127042] [10.1016/j.pestbp.2022.105180] |
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| 5. Li Bowen, Sun Shangde, Chen Xiaowei, Zhang Hao. (2022) Enzymatic conversion of soapstock fatty acids from oil refining waste to biosurfactant using a low-cost liquid lipase and a new application as an antioxidant. Biomass Conversion and Biorefinery, 14 (3): (3839-3851). [PMID:] [10.1007/s13399-022-02612-z] |
| 6. Lulu Dai, Haiming Gao, Hui Chen. (2021) Expression Levels of Detoxification Enzyme Genes from Dendroctonus armandi (Coleoptera: Curculionidae) Fed on a Solid Diet Containing Pine Phloem and Terpenoids. Insects, 12 (10): (926). [PMID:34680695] [10.3390/insects12100926] |
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| 8. Gao Haiming, Dai Lulu, Fu Danyang, Sun Yaya, Chen Hui. (2020) Isolation, Expression Profiling, and Regulation via Host Allelochemicals of 16 Glutathione S-Transferases in the Chinese White Pine Beetle, Dendroctonus armandi. Frontiers in Physiology, [PMID:33281609] [10.3389/fphys.2020.546592] |
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| 11. Lulu Dai, Haiming Gao, Jiaqi Ye, Danyang Fu, Yaya Sun, Hui Chen. (2018) Isolation of CarE genes from the Chinese white pine beetle Dendroctonus armandi (Curculionidae: Scolytinae) and their response to host chemical defense. PEST MANAGEMENT SCIENCE, 75 (4): (986-997). [PMID:30204286] [10.1002/ps.5205] |
| 12. Yi Feng, Shichang Liu, Guozhen Liu, Jianfeng Yao. (2016) Facile and fast removal of oil through porous carbon spheres derived from the fruit of Liquidambar formosana. CHEMOSPHERE, [PMID:27960116] [10.1016/j.chemosphere.2016.11.166] |
| 13. Lulu Dai, Junning Ma, Mingyuan Ma, Haoqiang Zhang, Qi Shi, Ranran Zhang, Hui Chen. (2015) Characterisation of GST genes from the Chinese white pine beetle Dendroctonus armandi (Curculionidae: Scolytinae) and their response to host chemical defence. PEST MANAGEMENT SCIENCE, 72 (4): (816-827). [PMID:26079390] [10.1002/ps.4059] |
| 14. Guofan Wang, Tao Wang, Tanrui Xi, Yangfan Sun, Ke Wan, Qingshan Li, Yuanna Sun. (2025) Effect of dispersed dot cathode configuration on the performance of La0.95Ag0.05CoO3 based anode-supported solid oxide fuel cells. Materials Science and Engineering B-Advanced Functional Solid-State Materials, [PMID:] [10.1016/j.mseb.2025.118641] |
| 15. Yaoyi Hu, Xiqiang Yuan, Zhengquan Zhang, Yu Zhang, Han Ma, Yunfei He, Shaoyun Shan, Tianding Hu. (2025) Preparation of solid superacid catalyst Al2(SO4)3/ZrO2-TiO2 and its mechanism of borneol synthesis from pinene. CATALYSIS TODAY, [PMID:] [10.1016/j.cattod.2025.115367] |
| 16. Kuo Zhao, Yunbo Shi, Haodong Niu, Qinglong Chen, Jinzhou Liu, Bolun Tang, Canda Zheng. (2025) Polyaniline/Tungsten Disulfide Composite for Room-Temperature NH3 Detection with Rapid Response and Low-PPM Sensitivity. SENSORS, 25 (13): (3948). [PMID:40648203] [10.3390/s25133948] |
| 17. Zuorong Huang, Quanquan Tang, Jing He, Lei Wu, Fengmin Liu, Xishuang Liang, Bin Wu, Mingliang Fu, Geyu Lu. (2025) High-Temperature CO2 Sensor with Second-Level Response for Diesel Engine Exhaust Gas Detection Applications. ACS Sensors, [PMID:41060794] [10.1021/acssensors.5c02897] |
| 18. Taozhong Zhang, Wanzhong Yin, Jin Yao, Weifan Du, Xiaoqi Ban, Wenju Sun, Chao Yin. (2026) High-efficiency molybdenite–galena flotation separation enabled by 4,6-diamino-2-mercaptopyrimidine as a novel selective depressant: Experimental evaluation and surface interaction mechanism. MINERALS ENGINEERING, [PMID:] [10.1016/j.mineng.2026.110367] |
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