Cas no 542-10-9 (Ethylidene diacetate)
Ethylidene diacetate Chemical and Physical Properties
Names and Identifiers
-
- Ethane-1,1-diyl diacetate
- 1,1-Ethanediol diacetate
- Ethylidene diacetate
- 1-(Acetyloxy)ethyl acetate
- 1,1-Di(acetyloxy)ethane
- 1,1-Diacetoxy-aethan
- 1,1-diacetoxy-ethane
- Acetaldehyde diacetate
- Acetaldehyde diacetyl acetal
- Aethylidenglykol-diacetat
- Diacetic acid ethylidene
- Ethylidene acetate
- 1,1-Diacetoxyethane
- 1,1-Ethanediol, diacetate
- Polyoxymethylenes
- Delrin
- 1-acetoxyethyl acetate
- 1,1-Ethanediol, 1,1-diacetate
- 1-acetyloxyethyl acetate
- KL1S8V6W25
- Ethylidene diacetate, 99%
- Ethylidene di(acetate)
- 1,1-EthanediolDiacetate
- 1,1'-Diacetoxy-ethane
- DSSTox_CID_7188
- AI3-24218
- CHEMBL3187663
- MFCD00014980
- Tox21_200113
- DTXSID1027188
- Q15720555
- EINECS 208-800-3
- SCHEMBL987906
- CS-0206532
- CAS-542-10-9
- NS00032998
- (2-BENZYLOXY-PHENYL)-HYDRAZINEHYDROCHLORIDE
- FT-0625724
- NCGC00248529-01
- AKOS015900230
- DTXCID507188
- NCGC00257667-01
- NSC 8852
- InChI=1/C6H10O4/c1-4(7)9-6(3)10-5(2)8/h6H,1-3H
- D90424
- AS-57369
- UNII-KL1S8V6W25
- 1-(Acetyloxy)ethyl acetate #
- NSC-8852
- 542-10-9
- NSC8852
- ETHYLIDENE DIACETATE [MI]
- 66455-31-0
-
- MDL: MFCD00014980
- Inchi: 1S/C6H10O4/c1-4(7)9-6(3)10-5(2)8/h6H,1-3H3
- InChI Key: ACKALUBLCWJVNB-UHFFFAOYSA-N
- SMILES: O(C(C)=O)C(C)OC(C)=O
Computed Properties
- Exact Mass: 146.05800
- Monoisotopic Mass: 146.058
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 10
- Rotatable Bond Count: 4
- Complexity: 125
- 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
- Topological Polar Surface Area: 52.6
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 0.5
Experimental Properties
- Color/Form: It has a strong fruit aroma
- Density: 1,07 g/cm3
- Melting Point: 18.85°C
- Boiling Point: 167°C
- Flash Point: 68 oC
- Refractive Index: 1.3995-1.4015
- PSA: 52.60000
- LogP: 0.45860
- Vapor Pressure: 1.7±0.3 mmHg at 25°C
- Solubility: Slightly soluble in water, easily soluble in ethanol and ether.
- Merck: 3811
Ethylidene diacetate Security Information
- Prompt:warning
- Signal Word:warning
- Hazard Statement: H227
- Warning Statement: P210-P280-P370+P378-P403+P235-P501
- Hazardous Material transportation number:UN 3272
- Hazard Category Code: R10: flammable.
- Safety Instruction: S24/25
- Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)
- Packing Group:III
- Hazard Level:3.2
- Safety Term:3.2
- Packing Group:III
- Risk Phrases:R10
- HazardClass:3.2
- PackingGroup:III
Ethylidene diacetate Customs Data
- HS CODE:2915390090
- Customs Data:
China Customs Code:
2915390090Overview:
2915390090. Other acetate esters. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:AB(Customs clearance form for Inbound Goods,Customs clearance form for outbound goods). MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Regulatory conditions:
A.Customs clearance form for Inbound Goods
B.Customs clearance form for outbound goodsInspection and quarantine category:
R.Sanitary supervision and inspection of imported food
S.Sanitary supervision and inspection of exported food
M.Import commodity inspection
N.Export commodity inspectionSummary:
2915390090. esters of acetic acid. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:5.5%. General tariff:30.0%
Ethylidene diacetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | E156139-25G |
Ethylidene diacetate |
542-10-9 | >98.0%(GC) | 25g |
¥934.90 | 2023-09-03 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | E916484-1g |
1,1-Ethanediol Diacetate |
542-10-9 | >98.0%(GC) | 1g |
¥180.00 | 2022-01-10 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | E916484-5g |
1,1-Ethanediol Diacetate |
542-10-9 | >98.0%(GC) | 5g |
¥398.00 | 2022-01-10 | |
| Apollo Scientific | OR938851-1g |
1,1-Ethanediol diacetate |
542-10-9 | 98+% | 1g |
£18.00 | 2025-03-21 | |
| Apollo Scientific | OR938851-5g |
1,1-Ethanediol diacetate |
542-10-9 | 98+% | 5g |
£54.00 | 2025-02-20 | |
| Apollo Scientific | OR938851-25g |
1,1-Ethanediol diacetate |
542-10-9 | 98+% | 25g |
£253.00 | 2025-02-20 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | E0030-25G |
1,1-Ethanediol Diacetate |
542-10-9 | >98.0%(GC) | 25g |
¥920.00 | 2024-04-16 | |
| abcr | AB135616-25 g |
1,1-Ethanediol diacetate, 98%; . |
542-10-9 | 98% | 25g |
€162.30 | 2022-06-12 | |
| Aaron | AR00DAW3-10g |
ETHYLIDENE DIACETATE |
542-10-9 | 98% | 10g |
$72.00 | 2025-01-24 | |
| Apollo Scientific | OR938851-100g |
1,1-Ethanediol diacetate |
542-10-9 | 98+% | 100g |
£998.00 | 2025-02-20 |
Ethylidene diacetate Suppliers
Ethylidene diacetate Related Literature
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1. Catalytic oxidative C–C bond cleavage route of levulinic acid and methyl levulinateFei Xia,Zhongtian Du,Junxia Liu,Yangyang Ma,Jie Xu RSC Adv. 2016 6 72744
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Chi-Tung Yeung,Ho-Lun Yeung,Wesley Ting Kwok Chan,Siu-Cheong Yan,Eric C. Y. Tam,Ka-Leung Wong,Chi-Sing Lee,Wing-Tak Wong CrystEngComm 2013 15 836
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3. 320. Kinetics of the acid-catalysed hydrolysis and decomposition of ethylidene diacetateR. P. Bell,B. Lukianenko J. Chem. Soc. 1957 1686
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Giovanni Carini Jr.,Francesco Parrino,Giovanni Palmisano,Gabriele Scandura,Ilaria Citro,Giuseppe Calogero,Antonino Bartolotta,Gaetano Di Marco Photochem. Photobiol. Sci. 2015 14 1685
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R. P. Bell,R. Le G. Burnett Trans. Faraday Soc. 1939 35 474
Related Categories
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid esters
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Carboxylic acid derivatives Carboxylic acid esters
- Solvents and Organic Chemicals Organic Compounds Acids/Esters
Additional information on Ethylidene diacetate
Ethylidene diacetate (CAS No. 542-10-9): A Comprehensive Overview in Modern Chemical Research
Ethylidene diacetate, chemically identified by the CAS number 542-10-9, is a versatile organic compound that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, with its unique structural and chemical properties, finds applications across various domains, including synthetic chemistry, material science, and biochemical studies. The molecular structure of ethylidene diacetate consists of an ethylene bridge linked to two acetate groups, which contributes to its reactivity and utility in multiple chemical transformations.
The significance of ethylidene diacetate in contemporary research is underscored by its role as a key intermediate in the synthesis of more complex molecules. Its bifunctional nature allows it to participate in a wide range of reactions, making it a valuable tool for chemists working on drug development and material innovation. Recent studies have highlighted its potential in facilitating the formation of carbon-carbon bonds, which is crucial for constructing intricate molecular architectures.
In the realm of pharmaceutical research, ethylidene diacetate has been explored for its ability to serve as a precursor in the synthesis of various pharmacologically active compounds. Researchers have leveraged its reactive sites to develop novel therapeutic agents targeting different biological pathways. For instance, derivatives of ethylidene diacetate have been investigated for their antimicrobial and anti-inflammatory properties, demonstrating promising results in preclinical trials.
The compound's applications extend beyond pharmaceuticals into the realm of materials science. Its incorporation into polymer matrices has been shown to enhance thermal stability and mechanical strength, making it a candidate for advanced composite materials. These materials are increasingly sought after in industries requiring high-performance components, such as aerospace and automotive sectors. The ability of ethylidene diacetate to modify polymer properties underscores its importance in developing next-generation materials with tailored functionalities.
From a synthetic chemistry perspective, ethylidene diacetate offers a unique platform for exploring new reaction pathways and methodologies. Its reactivity allows for the introduction of diverse functional groups, enabling the construction of complex organic molecules with precision. This has led to innovative approaches in catalysis and organic synthesis, where ethylidene diacetate acts as a crucial building block. The compound's versatility has also made it a subject of interest in green chemistry initiatives, as researchers seek sustainable alternatives for traditional synthetic routes.
The biochemical applications of ethylidene diacetate are equally compelling. Studies have indicated its potential role in modulating enzymatic activities and interacting with biological targets. By serving as a scaffold for drug-like molecules, it contributes to the discovery of new bioactive compounds with therapeutic potential. These findings highlight the compound's significance not only as a chemical intermediate but also as a catalyst for advancing our understanding of biological systems.
In conclusion, the multifaceted applications of Ethylidene diacetate (CAS No. 542-10-9) underscore its importance in modern chemical research. From facilitating complex synthetic transformations to contributing to advancements in pharmaceuticals and materials science, this compound continues to be a cornerstone in numerous scientific endeavors. As research progresses, it is likely that new applications and insights into the capabilities of Ethylidene diacetate will emerge, further solidifying its role as a vital component in the chemical landscape.
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