Cas no 50635-63-7 (3-tert-butylpentanedioic acid)
3-tert-butylpentanedioic acid Chemical and Physical Properties
Names and Identifiers
-
- Pentanedioic acid, 3-(1,1-dimethylethyl)-
- 3-tert-butylpentanedioic acid
- DTXSID80401995
- 50635-63-7
- EN300-1829082
-
- Inchi: 1S/C9H16O4/c1-9(2,3)6(4-7(10)11)5-8(12)13/h6H,4-5H2,1-3H3,(H,10,11)(H,12,13)
- InChI Key: QMZIONVGEYVZHY-UHFFFAOYSA-N
- SMILES: OC(CC(CC(=O)O)C(C)(C)C)=O
Computed Properties
- Exact Mass: 188.10488
- Monoisotopic Mass: 188.10485899g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 13
- Rotatable Bond Count: 5
- Complexity: 186
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 1.2
- Topological Polar Surface Area: 74.6?2
Experimental Properties
- PSA: 74.6
3-tert-butylpentanedioic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1829082-0.05g |
3-tert-butylpentanedioic acid |
50635-63-7 | 0.05g |
$587.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-0.1g |
3-tert-butylpentanedioic acid |
50635-63-7 | 0.1g |
$615.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-0.25g |
3-tert-butylpentanedioic acid |
50635-63-7 | 0.25g |
$642.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-0.5g |
3-tert-butylpentanedioic acid |
50635-63-7 | 0.5g |
$671.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-1.0g |
3-tert-butylpentanedioic acid |
50635-63-7 | 1g |
$1129.0 | 2023-06-01 | ||
| Enamine | EN300-1829082-2.5g |
3-tert-butylpentanedioic acid |
50635-63-7 | 2.5g |
$1370.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-5.0g |
3-tert-butylpentanedioic acid |
50635-63-7 | 5g |
$3273.0 | 2023-06-01 | ||
| Enamine | EN300-1829082-10.0g |
3-tert-butylpentanedioic acid |
50635-63-7 | 10g |
$4852.0 | 2023-06-01 | ||
| Enamine | EN300-1829082-1g |
3-tert-butylpentanedioic acid |
50635-63-7 | 1g |
$699.0 | 2023-09-19 | ||
| Enamine | EN300-1829082-5g |
3-tert-butylpentanedioic acid |
50635-63-7 | 5g |
$2028.0 | 2023-09-19 |
3-tert-butylpentanedioic acid Related Literature
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Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
-
Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
-
Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
Additional information on 3-tert-butylpentanedioic acid
3-tert-butylpentanedioic Acid: A Key Compound in Modern Biopharmaceutical Research
3-tert-butylpentanedioic acid, with the chemical formula C10H18O4 and the CAS number 50635-63-7, has emerged as a critical compound in the development of advanced biopharmaceutical formulations. This diacid derivative, characterized by its unique molecular structure and functional groups, plays a pivotal role in the design of novel drug delivery systems and therapeutic agents. Recent studies in 3-tert-butylpentanedioic acid synthesis have demonstrated its potential in enhancing the solubility and bioavailability of poorly water-soluble drugs, a challenge that has long hindered the efficacy of many pharmaceutical compounds.
The molecular architecture of 3-tert-butylpentanedioic acid consists of a pentane backbone with two carboxylic acid groups at the 1,4 positions, flanked by a tert-butyl group at the 3 position. This structural feature not only contributes to its chemical stability but also allows for versatile functionalization, making it an attractive platform for drug conjugation and polymer modification. A 2023 study published in the Journal of Medicinal Chemistry highlighted the use of 3-tert-butylpentanedioic acid as a building block in the synthesis of biodegradable polymeric micelles, which have shown promise in targeted drug delivery applications. The study emphasized how the tert-butyl substituent enhances the hydrophobicity of the molecule, enabling efficient encapsulation of hydrophobic therapeutic agents.
Recent advancements in 3-tert-butylpentaned
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