Cas no 2923-18-4 (Sodium trifluoroacetate)
Sodium trifluoroacetate Chemical and Physical Properties
Names and Identifiers
-
- SODIUM TRIFLUOROACETATE
- TRIFLUOROACETIC ACID SODIUM SALT
- sodiumperfluoroacetate
- trifluoro-aceticacisodiumsalt
- Sodlium trifluoroacetate
- TRIFLUOROACETIC ACID SODIUM CRYSTALLINE
- Acetic acid, trifluoro-, sodium salt
- SODIUMTRIFLUOR-ACETATE
- SODIUMPERFLUOROACETICACID
- Natriumtrifluoracetat
- Sodium 2,2,2-trifluoroacetate
- Sodiun trifluoroacetate
- EINECS 220-879-6
- sodium 2,2,2-trifluoroethanoate
- Trifluoroacetate sodium
- Trifluoroacetic acid sodium
- Sodium perfluoroacetate
- trifluoroacetic acid,sodium salt
- Acetic acid, 2,2,2-trifluoro-, sodium salt (1:1)
- Trifluoroacetic acid, sodium salt, 97%
- Trifluoroacetic acid, sodium salt
- sodium trifluoracetate
- CF3COONa
- sodium trifluoro-acetate
- CF3CO2Na
- NaO2CCF3;
- C2F3NaO2
- SY001632
- BP-31173
- E79457
- DTXCID9037957
- 2923-18-4
- NSC-118111
- SODIUM TRIFLUOROACETATE [USP-RS]
- 255JUV5YVI
- NS00083080
- UNII-255JUV5YVI
- SODIUM TRIFLUOROACETATE (USP-RS)
- sodium2,2,2-trifluoroacetate
- MFCD00013217
- CS-W017765
- DB-047551
- AKOS015852669
- Q25474224
- Sodium Trifluoroacetate-13C2
- Q-102549
- Acetic acid, 2,2,2trifluoro, sodium salt (1:1)
- DTXSID0062715
- Acetic acid, trifluoro, sodium salt
- T1336
- NSC 118111
- CHEMBL559917
- SCHEMBL96619
- Sodium trifluoroacetate
-
- MDL: MFCD00013217
- Inchi: 1S/C2HF3O2.Na/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1
- InChI Key: UYCAUPASBSROMS-UHFFFAOYSA-M
- SMILES: [Na+].FC(C(=O)[O-])(F)F
- BRN: 3597949
Computed Properties
- Exact Mass: 135.97500
- Monoisotopic Mass: 135.975
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 8
- Rotatable Bond Count: 0
- Complexity: 87.8
- Covalently-Bonded Unit Count: 2
- 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: nothing
- Topological Polar Surface Area: 40.1
Experimental Properties
- Color/Form: White powder
- Density: 1.49?g/mL(lit.)
- Melting Point: 207°C(dec.)(lit.)
- Boiling Point: 72.2 °C at 760 mmHg Vapour
- Flash Point: °C
- PH: 7 (H2O, 20℃)
- Solubility: H2O: 1?M at?20?°C, clear, colorless
- Water Partition Coefficient: 625 g/L (25 oC)
- PSA: 40.13000
- LogP: -0.70140
- Sensitiveness: Hygroscopic
- Solubility: Soluble in water and hot ethanol, slightly soluble in ether, insoluble in benzene and chlorohydrocarbons
Sodium trifluoroacetate Security Information
-
Symbol:
- Prompt:dangerous
- Signal Word:Warning
- Hazard Statement: H315,H319,H335
- Warning Statement: P261,P305+P351+P338
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:1
- Hazard Category Code: R36/37/38
- Safety Instruction: S26-S36-S37/39
- FLUKA BRAND F CODES:3-10
- RTECS:AK0250000
-
Hazardous Material Identification:
- HazardClass:6.1
- TSCA:T
- PackingGroup:II
- Storage Condition:Store in tightly closed containers. Store in a cool, dry, well ventilated area away from incompatible substances. Toxic rooms are locked. Avoid moisture.
- Packing Group:I; II; III
- Risk Phrases:R36/37/38
Sodium trifluoroacetate Customs Data
- HS CODE:29159080
- Customs Data:
China Customs Code:
2915900090Overview:
2915900090. Other saturated acyclic monocarboxylic acids and their anhydrides(Acyl halide\Peroxygenation)Chemicals\Peroxy acid and its halogenation\nitrification\sulfonation\Nitrosative derivative. VAT:17.0%. Tax refund rate:9.0%. 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:
2915900090 other saturated acyclic monocarboxylic acids and their anhydrides, halides, peroxides and peroxyacids; their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:5.5% General tariff:30.0%
Sodium trifluoroacetate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Fluorochem | 003595-1g |
Trifluoroacetic acid, sodium salt |
2923-18-4 | 98% | 1g |
£10.00 | 2022-03-01 | |
| Fluorochem | 003595-10g |
Trifluoroacetic acid, sodium salt |
2923-18-4 | 98% | 10g |
£12.00 | 2022-03-01 | |
| Fluorochem | 003595-50g |
Trifluoroacetic acid, sodium salt |
2923-18-4 | 98% | 50g |
£19.00 | 2022-03-01 | |
| Fluorochem | 003595-100g |
Trifluoroacetic acid, sodium salt |
2923-18-4 | 98% | 100g |
£35.00 | 2022-03-01 | |
| Fluorochem | 003595-250g |
Trifluoroacetic acid, sodium salt |
2923-18-4 | 98% | 250g |
£72.00 | 2022-03-01 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | T1336-500G |
Sodium Trifluoroacetate |
2923-18-4 | >98.0%(T) | 500g |
¥1990.00 | 2024-04-15 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | S101693-500g |
Sodium trifluoroacetate |
2923-18-4 | 97% | 500g |
¥272.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | S101693-100g |
Sodium trifluoroacetate |
2923-18-4 | 97% | 100g |
¥126.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | S101693-5g |
Sodium trifluoroacetate |
2923-18-4 | 97% | 5g |
¥29.90 | 2023-09-01 | |
| SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd. | S101693-25g |
Sodium trifluoroacetate |
2923-18-4 | 97% | 25g |
¥65.90 | 2023-09-01 |
Sodium trifluoroacetate Suppliers
Sodium trifluoroacetate Related Literature
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Yiu-Tung Wong,Wing-Ki Law,Shirley Sau-Ling Lai,Siu-Pan Wong,Kong-Chi Lau,Clare Ho Anal. Methods 2018 10 3514
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Kotaro Satoh,Hideyuki Hashimoto,Shinya Kumagai,Hiroshi Aoshima,Mineto Uchiyama,Ryoma Ishibashi,Yuuma Fujiki,Masami Kamigaito Polym. Chem. 2017 8 5002
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Cristina Ruiz Martínez,Juana M. Pérez,Francisco M. Arrabal-Campos,María Batuecas,Manuel A. Ortu?o,Ignacio Fernández Polym. Chem. 2021 12 4083
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Hao Dong,Ling-Dong Sun,Ye-Fu Wang,Jia-Wen Xiao,Datao Tu,Xueyuan Chen,Chun-Hua Yan J. Mater. Chem. C 2016 4 4186
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Lewis D. Blackman,Kay E. B. Doncom,Matthew I. Gibson,Rachel K. O'Reilly Polym. Chem. 2017 8 2860
Related Categories
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Alpha-halocarboxylic acids
- Solvents and Organic Chemicals Organic Compounds Organic acids and derivatives Carboxylic acids and derivatives Alpha-halocarboxylic acids and derivatives Alpha-halocarboxylic acids
- Solvents and Organic Chemicals Organic Compounds Acids/Esters
Additional information on Sodium trifluoroacetate
Introduction to Sodium trifluoroacetate (CAS No. 2923-18-4)
Sodium trifluoroacetate, a compound with the chemical formula C?HNaFO?, is a significant reagent in the field of organic synthesis and pharmaceutical research. Its molecular structure incorporates a trifluoroacetate group, which imparts unique chemical properties making it invaluable in various applications. This introduction delves into the compound's characteristics, applications, and recent advancements in research where Sodium trifluoroacetate plays a pivotal role.
The CAS number 2923-18-4 uniquely identifies Sodium trifluoroacetate among other chemical substances. This numbering system ensures precise classification and communication within the scientific community. The compound is primarily recognized for its role as a salt form of trifluoroacetic acid, offering enhanced solubility and stability compared to its acidic counterpart. These attributes make it a preferred choice in synthetic chemistry, particularly in the preparation of complex molecules.
Sodium trifluoroacetate finds extensive use in pharmaceutical synthesis due to its ability to facilitate various reactions under mild conditions. Its application in the synthesis of active pharmaceutical ingredients (APIs) has been increasingly explored. Recent studies have highlighted its utility in the preparation of fluorinated compounds, which are crucial in developing modern drugs targeting neurological disorders and cancer. The unique electronic properties of fluorine atoms significantly influence the bioactivity and metabolic stability of these drugs, making Sodium trifluoroacetate an essential reagent in this domain.
In addition to pharmaceuticals, Sodium trifluoroacetate is widely employed in materials science and catalysis. Its ability to act as a ligand in transition metal catalysis has been leveraged to develop novel catalysts for asymmetric synthesis. These catalysts are instrumental in producing enantiomerically pure compounds, which are highly sought after in the pharmaceutical industry. The use of Sodium trifluoroacetate as a ligand has shown promise in enhancing reaction efficiency and selectivity, thereby reducing the environmental impact of synthetic processes.
Recent advancements in green chemistry have also seen the adoption of Sodium trifluoroacetate as an eco-friendly alternative to traditional acid catalysts. Its high thermal stability and compatibility with water make it an ideal candidate for solvent-free reactions, reducing the need for hazardous organic solvents. This aligns with global efforts to minimize the ecological footprint of chemical manufacturing processes. Research has demonstrated that reactions catalyzed by Sodium trifluoroacetate often proceed with higher yields and fewer byproducts compared to conventional methods.
The compound's role in peptide synthesis is another area of significant interest. Sodium trifluoroacetate is used to activate carboxyl groups for coupling reactions, enabling the efficient assembly of peptide chains. This application is particularly valuable in the development of peptide-based therapeutics, which have shown immense potential in treating various diseases, including infections and autoimmune disorders. The precision offered by Sodium trifluoroacetate in peptide bond formation ensures high fidelity in constructing these complex biomolecules.
In conclusion, Sodium trifluoroacetate (CAS No. 2923-18-4) is a versatile compound with broad applications across multiple scientific disciplines. Its unique chemical properties make it indispensable in pharmaceutical synthesis, materials science, and catalysis. The ongoing research into its applications underscores its importance as a reagent capable of driving innovation and sustainability in chemical processes. As scientific understanding evolves, it is expected that new uses for Sodium trifluoroacetate will continue to emerge, further solidifying its role as a cornerstone compound in modern chemistry.
2923-18-4 (Sodium trifluoroacetate) Related Products
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