Cas no 123-28-4 (Dilauryl thiodipropionate)
Dilauryl thiodipropionate Chemical and Physical Properties
Names and Identifiers
-
- Thiodipropionic acid didodecylester
- DLTP
- Didodecyl 3,3-thiodipropionate
- 3,3-Thiodipropionic acid di-n-dodecyl ester
- Dilauryl-3,3-thiodipropionate
- Antioxidant DLTDP
- Dilauryl Thiodipropionate
- Dydecyl Thiodipropionate
- Didodecyl 3,3'-Thiodipropionate
- Cyanox? LTDP
- 3,3'-Thiodipropionic Acid Didodecyl Ester
- 3,3'-Thiodipropionic acid dilauryl ester
- Antiox L
- Cyanox LTDP
- didodecyl thiodipropionate
- dilauryl
- dilauryl 3,3'-thiodipropionate
- Dilaurylthiopropionate
- DLT
- DLTDP
- DMPTP
- Lusmit
- milbanf
- tyoxb
- Tyox B
- 3,3-Thiodipropionic Acid Didodecyl Ester
- Carstab dltdp
- Neganox DLTP
- Antioxidant AS
- Stabilizer DLT
- Plastanox LTDP
- Milban F
- Antioxidant LTDP
- Ipognox 89
- Advastab 800
- D 1 (antioxidant)
- Irganox PS 800
- Plastanox LTDP Antioxidant
- Dilaurylthiodipropionate
- Lauryl 3,3'-thiodipropionate
- Thiobis(dodecyl propionate)
- Bis(dodecyloxycarbonylethyl) sulfide
- Propionic acid, 3,3'-thiodi-, didodecyl ester
- Propanoic ac
- Didodecyl 3,3 inverted exclamation mark -Thiodipropionate
- DILAURYL THIODIPROPIONATE [FCC]
- 123-28-4
- EINECS 204-614-1
- Dilauryl .beta.',.beta.'-thiodipropionate
- 3,3'-Thiodipropionic acid, bis-dodecyl ester
- 1ST2305-1000
- EC 204-614-1
- INS NO.389
- Dilauryl thiodipropionate, tech grade
- Plastic additive 16, European Pharmacopoeia (EP) Reference Standard
- 31852-09-2
- CCRIS 3936
- didodecyl 3,3'-thiodipropanoate
- Didodecyl thiobispropanoate
- Nonox DLTDP
- Thiodipropionic acid didodecyl ester
- T0205
- V51YH1B080
- DB-187094
- Propanoic acid, 3,3'-thiobis-, 1,1'-didodecyl ester
- Dilauryl thiodipropionic acid
- C30H58O4S
- Propanoic acid, 3,3'-thiobis-, didodecyl ester (9CI)
- Evanstab 12
- EINECS 250-841-4
- 1ST2305
- Plastic additive 9, United States Pharmacopeia (USP) Reference Standard
- Dilauryl beta-thiodipropionate
- CS-0152180
- 3,3'-Thiodipropionic acid di-n-dodecyl ester
- NS00003639
- Dilaurylester kyseliny .beta.',.beta.'-thiodipropionove
- Propanoic acid,3'-thiobis-, didodecyl ester
- WLN: 12OV2S2VO12
- D 1
- Propanoic acid 3,3'-thiobis(didodecyl) ester
- Propionic acid,3'-thiodi-, didodecyl ester
- AKOS015898624
- PLASTIC ADDITIVE 9
- NSC65494
- Lowinox DLTDP
- BRN 1808848
- DTXSID2026999
- HY-W099538
- Dilauryl .beta.-thiodipropionate
- 115628-90-5
- Dilaurylester kyseliny beta',beta'-thiodipropionove
- UNII-V51YH1B080
- Propanoic acid, thiobis-, didodecyl ester
- INS-389
- Arbestab DLTP
- DILAURYL THIODIPROPIONATE [HSDB]
- 3,3'-Thiobispropionic acid, didodecyl ester
- AI3-25277
- SCHEMBL42383
- E-389
- AC9074
- Propionic acid, 3,3'-thiobis-, didodecyl ester
- Q26840985
- MFCD00026589
- dilauryldithiopropionate
- NSC-65494
- 3,3'-Thiobis[propionic acid], didodecyl ester
- dodecyl 3-(3-dodecoxy-3-oxopropyl)sulanylpropanoate
- Thiodipropionic acid dilauryl ester
- Sumilizer TPL
- 3,3'-Thiodipropanoic acid,didodecyl ester
- Dilaurylester kyseliny beta',beta'-thiodipropionove [Czech]
- DIDODECYL 3,3?-THIODIPROPIONATE
- Rasumitto
- dilauryl-3,3'-thiodipropionate
- Propanoic acid, 3,3'-thiobis-, didodecyl ester
- 4-03-00-00744 (Beilstein Handbook Reference)
- SY052023
- Dilauryl .beta.,.beta.-thiodipropionate
- dodecyl 3-(3-dodecoxy-3-oxopropyl)sulfanylpropanoate
- PLASTIC ADDITIVE 9 [USP-RS]
- Didodecyl 3,3'-thiodipropionate, >97%
- Dilauryl .beta.,.beta.'-thiodipropionate
- 3, didodecyl ester
- Thiodipropionic acid, dilauryl ester
- LS-15303
- Propionic acid,3'-thiobis-, didodecyl ester
- Didodecyl 3,3'-thiodipropionate Solution in Acetonitrile, 1000mug/mL
- Argus DLTDP
- CHEBI:165384
- didodecyl 3,3'-sulfanediyldipropanoate
- DIDODECYL THIODIPROPANOATE [MI]
- dodecyl 3-{[3-(dodecyloxy)-3-oxopropyl]sulfanyl}propanoate
- 3,3'-Thiodipropionic Acid Didodecyl Ester; Didodecyl 3,3'-thiodipropionate
- Thiobis[dodecyl propionate]
- 53571-83-8
- NSC 65494
- HSDB 353
- MSK2305-1000
- AAA12328
- 204-614-1
- Dilauryl 3,3'thiodipropionate
- PLASTIC ADDITIVE 9 (USP-RS)
- Dilauryl betathiodipropionate
- Didodecyl 3,3'-thiodipropionate Solution in Acetonitrile, 1000?g/mL
- DILAURYLESTER KYSELINY BETA',BETA'-THIODIPROPIONOVE (CZECH)
- 3,3'Thiobispropionic acid, didodecyl ester
- Propionic acid, 3,3'thiobis, didodecyl ester
- Propanoic acid, 3,3'thiobis, didodecyl ester
- DIDODECYL THIODIPROPANOATE
- Dilauryl beta,beta'-thiodipropionate
- Propionic acid, 3,3'thiodi, didodecyl ester
- MSK2305
- Lauryl 3,3'thiodipropionate
- DILAURYL THIODIPROPIONATE [INCI]
- Dilaurylester kyseliny beta',beta'thiodipropionove
- Didodecyl 3,3'thiodipropionate
- Dilauryl thiodipropionate
-
- MDL： MFCD00026589
- Inchi： 1S/C30H58O4S/c1-3-5-7-9-11-13-15-17-19-21-25-33-29(31)23-27-35-28-24-30(32)34-26-22-20-18-16-14-12-10-8-6-4-2/h3-28H2,1-2H3
- InChI Key： GHKOFFNLGXMVNJ-UHFFFAOYSA-N
- SMILES： CCCCCCCCCCCCOC(CCSCCC(OCCCCCCCCCCCC)=O)=O
Computed Properties
- Exact Mass: 514.40600
- Monoisotopic Mass: 514.40558150g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 35
- Rotatable Bond Count: 30
- Complexity: 416
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 11.7
- Topological Polar Surface Area: 77.9
Experimental Properties
- Color/Form: White flocculent or flaky crystalline solid.
- Density: 0.915?g/mL?at 25?°C(lit.)
- Melting Point: 40-42?°C (lit.)
- Boiling Point: 570.34°C (rough estimate)
- Flash Point: Degrees Fahrenheit:235.4°F
Degrees Celsius:113°C - Refractive Index: 1.5220 (estimate)
- PSA: 77.90000
- LogP: 9.42800
- Vapor Pressure: 0.2 mmHg ( 163 °C)
- FEMA: 2377
- Solubility: Soluble in methanol, acetone, carbon tetrachloride and benzene, insoluble in water.
Dilauryl thiodipropionate Security Information
- Hazardous Material transportation number：NONH for all modes of transport
- WGK Germany：1
- RTECS：UF8000000
-
Hazardous Material Identification：
Dilauryl thiodipropionate Customs Data
- HS CODE：2930909090
- Customs Data：
China Customs Code:
2930909090Overview:
2930909090. Other organic sulfur compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%
Dilauryl thiodipropionate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | D128406-250G |
Dilauryl thiodipropionate |
123-28-4 | 250g |
￥637.92 | 2023-11-09 | ||
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | T0205-500G |
Didodecyl 3,3'-Thiodipropionate |
123-28-4 | >90.0%(GC) | 500g |
￥390.00 | 2024-04-18 | |
| TRC | D441730-10g |
Didodecyl 3,3'-Thiodipropionate |
123-28-4 | 10g |
$ 138.00 | 2023-09-07 | ||
| TRC | D441730-50g |
Didodecyl 3,3'-Thiodipropionate |
123-28-4 | 50g |
$161.00 | 2023-05-18 | ||
| TRC | D441730-100g |
Didodecyl 3,3'-Thiodipropionate |
123-28-4 | 100g |
$224.00 | 2023-05-18 | ||
| TRC | D441730-250g |
Didodecyl 3,3'-Thiodipropionate |
123-28-4 | 250g |
$276.00 | 2023-05-18 | ||
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | D830680-2.5kg |
Dilauryl thiodipropionate |
123-28-4 | 90% | 2.5kg |
1,088.00 | 2021-05-17 | |
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | 1545001-100MG |
Dilauryl thiodipropionate |
123-28-4 | 100mg |
￥3302.56 | 2025-01-16 | ||
| XI GE MA AO DE LI QI （ SHANG HAI ） MAO YI Co., Ltd. | P2155016 |
Dilauryl thiodipropionate |
123-28-4 | European Pharmacopoeia (EP) Reference Standard | ￥2654.27 | 2022-02-23 | ||
| BAI LING WEI Technology Co., Ltd. | 317091-25G |
Didodecyl 3,3'-Thiodipropionate, 99% |
123-28-4 | 99% | 25G |
￥ 185 | 2022-04-26 |
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Dilauryl thiodipropionate Related Literature
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1. Characterization of transients formed in aqueous solutions of substituted alkyl sulfides: a pulse radiolysis studyDilip K. Maity,Hari Mohan,Jai P. Mittal J. Chem. Soc. Faraday Trans. 1994 90 703
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Kirsten E. Overdahl,Rebecca Sutton,Jennifer Sun,Noelle J. DeStefano,Gordon J. Getzinger,P. Lee Ferguson Environ. Sci.: Processes Impacts 2021 23 429
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Shamala Salvamani,Baskaran Gunasekaran,Mohd Yunus Shukor,Md. Zuki Abu Bakar,Siti Aqlima Ahmad RSC Adv. 2016 6 32685
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Aurélie Cortéjade,Audrey Buleté,Laura Prouteau,Saber Chatti,Cécile Cren,Emmanuelle Vulliet Anal. Methods 2017 9 3549
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5. New epoxidation with m-chloroperbenzoic acid at elevated temperaturesY. Kishi,M. Aratani,H. Tanino,T. Fukuyama,T. Goto,S. Inoue,S. Sugiura,H. Kakoi J. Chem. Soc. Chem. Commun. 1972 64
Additional information on Dilauryl thiodipropionate
Dilauryl thiodipropionate (CAS No. 123-28-4): A Comprehensive Overview
Dilauryl thiodipropionate, with the chemical formula C??H??O?S and CAS number 123-28-4, is a compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, characterized by its unique molecular structure featuring lauryl groups and thiodipropionate moieties, exhibits a range of properties that make it valuable in various applications, particularly in the development of specialized materials and bioactive molecules.
The molecular structure of Dilauryl thiodipropionate consists of two lauryl chains (C??H??) linked by a thiodipropionate bridge (S-(CH?CH?COO)?). This configuration imparts upon it both hydrophobic and hydrophilic characteristics, making it an excellent candidate for use in formulations that require balance between lipophilicity and water solubility. The presence of the sulfur atom in the thiodipropionate moiety also contributes to its reactivity, enabling various chemical modifications that can be exploited in synthetic chemistry.
In recent years, Dilauryl thiodipropionate has been explored for its potential applications in pharmaceutical formulations. Its ability to form stable complexes with other molecules has made it a promising candidate for drug delivery systems. Specifically, researchers have been investigating its use as a component in micelles and liposomes, which are nanoscale vesicles capable of encapsulating therapeutic agents and delivering them to target sites in the body with high efficiency. This approach has shown particular promise in the treatment of chronic diseases where sustained release of medication is crucial.
Moreover, the chemical properties of Dilauryl thiodipropionate have been leveraged in the development of novel biomaterials. Its compatibility with various polymers and its ability to modify surface properties have led to its incorporation into coatings that enhance biocompatibility and reduce tissue rejection in medical implants. These advancements highlight the compound's versatility and its potential to contribute to significant improvements in medical technology.
The synthesis of Dilauryl thiodipropionate is another area where recent research has made notable progress. Traditional synthetic routes often involve harsh conditions and generate byproducts that can be challenging to handle. However, newer methodologies have focused on greener chemistry principles, utilizing catalytic processes that minimize waste and improve yield. One such approach involves the use of enzymatic catalysis, which offers a more environmentally friendly alternative to traditional chemical synthesis. These innovations not only enhance the efficiency of producing Dilauryl thiodipropionate but also align with global efforts to promote sustainable industrial practices.
In addition to its pharmaceutical applications, Dilauryl thiodipropionate has found utility in the cosmetics industry. Its emollient properties make it an effective ingredient in skincare products, where it helps to moisturize and protect the skin. Furthermore, its stability under various environmental conditions ensures that formulations containing this compound remain effective over longer periods, enhancing product shelf life. This has made it a preferred choice for cosmetic brands looking to develop high-performance skincare solutions.
The impact of Dilauryl thiodipropionate on material science is also noteworthy. Its ability to act as a crosslinking agent has been utilized in the production of advanced polymers that exhibit enhanced mechanical strength and thermal stability. These materials are particularly valuable in industries where durability and performance under extreme conditions are paramount, such as aerospace and automotive manufacturing. By incorporating this compound into polymer matrices, manufacturers can produce materials with improved properties that meet the rigorous demands of these sectors.
Epidemiological studies have also begun to explore the potential health benefits associated with exposure to Dilauryl thiodipropionate. While further research is needed to fully understand its effects on human health, preliminary findings suggest that it may have antioxidant properties that could help mitigate cellular damage caused by oxidative stress. This possibility opens up new avenues for therapeutic applications, particularly in age-related diseases where oxidative damage plays a significant role.
The regulatory landscape for compounds like Dilauryl thiodipropionate is continually evolving as new research emerges. Regulatory bodies are increasingly focused on ensuring that such compounds are safe for their intended applications while also considering environmental impact. Manufacturers must navigate these regulations carefully to ensure compliance while maintaining innovation in their product development processes. This dynamic regulatory environment underscores the importance of ongoing research and collaboration between scientists, regulators, and industry stakeholders.
In conclusion, Dilauryl thiodipropionate (CAS No. 123-28-4) is a multifaceted compound with a wide range of applications across multiple industries. From pharmaceuticals to cosmetics and material science, its unique properties make it a valuable asset in modern chemistry. As research continues to uncover new uses and refine synthetic methods, the potential applications for this compound are likely to expand even further, driving innovation and progress in numerous fields.
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