Online Database of Chemicals from Around the World

Octa(OtBu)-Glu-OtBu
[CAS# 1188328-39-3]

List of Suppliers
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Shandong Juntai Pharmaceutical Co., Ltd. China Inquire  
+86 15106953682
sales01@h2opharm.com
QQ chat
Chemical manufacturer since 2020
chemBlink standard supplier since 2024
Guangzhou Congen Pharmatec Co., Ltd. China Inquire  
+86 13380081396
marketing@congenpharm.com
Skype Chat
QQ chat
WeChat: Shine_Huang2014
WhatsApp: +8613242332900
Chemical manufacturer since 2013
chemBlink standard supplier since 2025
Complete supplier list of Octa(OtBu)-Glu-OtBu
Identification
Classification Pharmaceutical intermediate >> API intermediate
Name Octa(OtBu)-Glu-OtBu
Synonyms (4S)-5-tert-butoxy-4-[(18-tert-butoxy-18-oxo-octadecanoyl)amino]-5-oxo-pentanoic acid
Molecular Structure CAS # 1188328-39-3, Octa(OtBu)-Glu-OtBu, (4S)-5-tert-butoxy-4-[(18-tert-butoxy-18-oxo-octadecanoyl)amino]-5-oxo-pentanoic acid
Molecular Formula C31H57NO7
Molecular Weight 555.79
CAS Registry Number 1188328-39-3
SMILES CC(C)(C)OC(=O)CCCCCCCCCCCCCCCCC(=O)N[C@@H](CCC(=O)O)C(=O)OC(C)(C)C
Properties
Density 1.0±0.1 g/cm3, Calc.*
Index of Refraction 1.475, Calc.*
Boiling Point 665.4±45.0 ºC (760 mmHg), Calc.*
Flash Point 356.2±28.7 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319    Details
Precautionary Statements P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330    Details
SDS Available
up Discovory and Applicatios
Octa(OtBu)-Glu-OtBu, also known as octa-tert-butyl glutamate, is a synthetic compound that has attracted attention in the fields of organic chemistry and material science due to its unique structural features and potential applications. The compound consists of a glutamic acid backbone with eight tert-butyl (OtBu) groups attached, which significantly influences its physical and chemical properties.

The discovery of octa(OtBu)-Glu-OtBu can be traced back to research focused on the modification of amino acids to enhance their solubility and stability. Researchers aimed to create derivatives of glutamic acid that could retain the biological functions of the parent compound while improving their properties for various applications. The incorporation of tert-butyl groups was a strategic choice, as these bulky substituents are known to increase hydrophobicity, thereby enhancing solubility in organic solvents and reducing the compound's reactivity with water.

The synthesis of octa(OtBu)-Glu-OtBu typically involves a multi-step process. Initially, the glutamic acid backbone is protected to prevent unwanted reactions at the amino and carboxyl groups. Subsequently, tert-butyl groups are introduced through a process such as nucleophilic substitution or coupling reactions. The final product is then deprotected to yield the desired octa-substituted glutamate derivative. The synthetic pathway may vary depending on the specific reagents and conditions used, but the overall goal remains consistent: to produce a compound with enhanced solubility and stability.

One of the key applications of octa(OtBu)-Glu-OtBu is in the formulation of advanced materials, particularly in the development of polymers and polymeric composites. The introduction of octa-tert-butyl glutamate into polymer matrices can enhance the mechanical properties and thermal stability of the resulting materials. The compound's hydrophobic nature allows it to function as a plasticizer, improving the flexibility and processability of polymers, which is crucial for various industrial applications.

In addition to its role in material science, octa(OtBu)-Glu-OtBu has potential applications in the pharmaceutical and biomedical fields. The unique structure of the compound may be leveraged to develop drug delivery systems or as a carrier for therapeutic agents. By incorporating this compound into nanoparticles or liposomes, researchers aim to enhance the solubility and bioavailability of poorly water-soluble drugs, improving their therapeutic efficacy. The ability of octa-tert-butyl glutamate to interact with biological membranes may also provide insights into its potential as a drug delivery vehicle.

Moreover, the compound's functional groups can serve as reactive sites for further chemical modifications, allowing for the development of a diverse range of derivatives tailored for specific applications. The versatility of octa(OtBu)-Glu-OtBu in creating new materials and enhancing existing ones highlights its significance in ongoing research and development efforts.

In summary, octa(OtBu)-Glu-OtBu represents a significant advancement in the field of organic chemistry, particularly in the synthesis of modified amino acids with enhanced properties. Its potential applications in material science and pharmaceuticals demonstrate the compound's versatility and promise for future research. As scientists continue to explore the properties and applications of octa(OtBu)-Glu-OtBu, it is likely that new and innovative uses will emerge, further establishing its importance in various fields.
Market Analysis Reports
List of Reports Available for Octa(OtBu)-Glu-OtBu
Related Products
N-Octanoyl-homoserine lactone  N-Octanoyl-N-methylglucamine  N-Octanoylmorpholine  2-Octanoyloxybenzoic acid  4-Octanoylphenethyl acetate  5-Octanoylsalicylic acid  N-Octanoyl-D-erythro-sphingosine  3-Octanoylthiopropyltriethoxysilane  4-Octanoyl-1-vinylbenzene  Octan-2-yl 2-cyanoacetate  5,8,11,14,17,20,23,26-Octaoxa-2-azanonacosanedioic acid 1-(9H-fluoren-9-ylmethyl) ester  (-)-1,2-Octanediol  (R)-Octane-1,2-diol  1,3-Octanediol  3,6-Octanedione  1,8-Octanedithiol  N,N'-(Octane-1,8-diyl)bis(P,P-di(aziridin-1-yl)phosphinothioic amide)  N,N'-1,8-Octanediylbis[2,2-dichloro]acetamide  Octanenitrile  1-Octanesulfonic acid sodium salt monohydrate