Determine the necessary mass, volume, or concentration for preparing a solution.
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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
T168318-100mg
|
100mg |
3
|
$9.90
|
|
|
T168318-250mg
|
250mg |
3
|
$11.90
|
|
|
T168318-1g
|
1g |
3
|
$14.90
|
|
|
T168318-5g
|
5g |
3
|
$18.90
|
|
|
T168318-10g
|
10g |
5
|
$30.90
|
|
|
T168318-25g
|
25g |
2
|
$54.90
|
|
|
T168318-100g
|
100g |
1
|
$144.90
|
|
| Synonyms | DTXSID5066534 | 1,14-Dihydroxytetradecane | 1,14-Tetradecanol | BDBM36276 | J-012793 | DS-6571 | MFCD00004758 | 1,14-Tetradecandiol | AKOS015856535 | EINECS 243-341-2 | FT-0606053 | 1,14-Tetradecanediol | SCHEMBL158466 |
|---|---|
| Specifications & Purity | ≥97% |
| Storage Temp | Room temperature |
| Shipped In | Normal |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty alcohols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Long-chain fatty alcohols |
| Alternative Parents | Primary alcohols Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Long chain fatty alcohol - Organic oxygen compound - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Alcohol - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. |
| External Descriptors | Not available |
|
|
|
| Pubchem Sid | 504755924 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504755924 |
| IUPAC Name | tetradecane-1,14-diol |
| INCHI | InChI=1S/C14H30O2/c15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16/h15-16H,1-14H2 |
| InChIKey | XLKZJJVNBQCVIX-UHFFFAOYSA-N |
| Smiles | C(CCCCCCCO)CCCCCCO |
| Isomeric SMILES | C(CCCCCCCO)CCCCCCO |
| PubChem CID | 88261 |
| Molecular Weight | 230.39 |
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 | Jun 10, 2025 | T168318 | |
| Certificate of Analysis | Jun 10, 2025 | T168318 | |
| Certificate of Analysis | Sep 20, 2024 | T168318 | |
| Certificate of Analysis | Sep 20, 2024 | T168318 | |
| Certificate of Analysis | Sep 20, 2024 | T168318 | |
| Certificate of Analysis | Sep 20, 2024 | T168318 | |
| Certificate of Analysis | Jul 06, 2023 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 | |
| Certificate of Analysis | Dec 22, 2021 | T168318 |
| Melt Point(°C) | 85-90°C |
|---|---|
| Molecular Weight | 230.390 g/mol |
| XLogP3 | 4.600 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 13 |
| Exact Mass | 230.225 Da |
| Monoisotopic Mass | 230.225 Da |
| Topological Polar Surface Area | 40.500 Ų |
| Heavy Atom Count | 16 |
| Formal Charge | 0 |
| Complexity | 101.000 |
| 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. Zhenwei Zhang, Xiaoshi Ma, Chuanjun Yue, Xuejiao Wei, Baoliang Liu, Xiaohui Chen. (2022) Waste alkaline Mn–Zn batteries as efficient catalysts applied in ketonization of fatty acids. Sustainable Chemistry and Pharmacy, 29 (100787). |
| 2. Qianru Wanyan, Yaxin Qiu, Wenting Zhang, Hai Yu, Defeng Wu. (2021) Functional biopolyesters based on cross-linked Poly(L-malic acid): Network engineering towards tailoring brittle-ductile transition and shape-memory performance. POLYMER, 221 (123628). |
| 3. Yiyang Gu, Chunyu Ru, Zhen Zhao, Danming Chao, Xincai Liu. (2020) Performance enhancement of shape memory poly(aryl ether ketone) via photodimerization of pendant anthracene units. EUROPEAN POLYMER JOURNAL, 123 (109413). |