2-Thenoyltrifluoroacetone
(Synonyms: 2-噻吩甲酰三氟丙酮,HTTA; TTA; TTFA) 目录号 : GC42193
An inhibitor of respiration
Cas No.:326-91-0
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
2-Thenoyltrifluoroacetone (TTFA) is an inhibitor of respiration in animals and bacteria. In animals, TTFA binds at the quinone reduction site of succinate:ubiquinone oxidoreductase (SQR; Complex II), preventing ubiquinone from binding. It inhibits NADH fumarate reductase in bacteria. TTFA also inhibits photosystem II in plants and NADH-ubiquinone oxidoreductase of the virus Vibrio cholerae, decreasing cholera toxin production. This compound is also a chelator of metals, including lanthanum, zirconium, hafnium, and neodymium.
| Cas No. | 326-91-0 | SDF | |
| 别名 | 2-噻吩甲酰三氟丙酮,HTTA; TTA; TTFA | ||
| Canonical SMILES | O=C(C1=CC=CS1)CC(C(F)(F)F)=O | ||
| 分子式 | C8H5F3O2S | 分子量 | 222.2 |
| 溶解度 | DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 30 mg/ml | 储存条件 | Store at -20°C |
| General tips | 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液；一旦配成溶液，请分装保存，避免反复冻融造成的产品失效。 储备液的保存方式和期限：-80°C 储存时，请在 6 个月内使用，-20°C 储存时，请在 1 个月内使用。 为了提高溶解度，请将管子加热至37℃，然后在超声波浴中震荡一段时间。 |
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| Shipping Condition | 评估样品解决方案：配备蓝冰进行发货。所有其他可用尺寸：配备RT，或根据请求配备蓝冰。 | ||
| 制备储备液 | |||
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1 mg | 5 mg | 10 mg |
| 1 mM | 4.5005 mL | 22.5023 mL | 45.0045 mL |
| 5 mM | 0.9001 mL | 4.5005 mL | 9.0009 mL |
| 10 mM | 0.45 mL | 2.2502 mL | 4.5005 mL |
| 第一步：请输入基本实验信息（考虑到实验过程中的损耗，建议多配一只动物的药量） | ||||||||||
| 给药剂量 | mg/kg |  |
动物平均体重 | g | |
每只动物给药体积 | ul | |
动物数量 | 只 |
| 第二步：请输入动物体内配方组成（配方适用于不溶于水的药物；不同批次药物配方比例不同，请联系GLPBIO为您提供正确的澄清溶液配方） | ||||||||||
| % DMSO % % Tween 80 % saline | ||||||||||
| 计算重置 | ||||||||||
计算结果:
工作液浓度： mg/ml；
DMSO母液配制方法： mg 药物溶于 μL DMSO溶液（母液浓度 mg/mL，
体内配方配制方法：取 μL DMSO母液，加入 μL PEG300，混匀澄清后加入μL Tween 80，混匀澄清后加入 μL saline，混匀澄清。
1. 首先保证母液是澄清的；
2.
一定要按照顺序依次将溶剂加入，进行下一步操作之前必须保证上一步操作得到的是澄清的溶液，可采用涡旋、超声或水浴加热等物理方法助溶。
3. 以上所有助溶剂都可在 GlpBio 网站选购。
Thenoyltrifluoroacetone (TTA)-Carbon Dot/Aerogel Fluorescent Sensor for Lanthanide and Actinide Ions
ACS Omega 2017 Dec 29;2(12):9288-9295.PMID:31457442DOI:10.1021/acsomega.7b01883.
Contamination of groundwater with radioactive substances comprising actinides and lanthanides is a significant environmental hazard and thus the development of selective, sensitive, and easy-to-apply sensors for water-soluble actinide and lanthanide ions is highly sought. We constructed a new selective fluorescent sensor for UO2 2+, Sm3+, and Eu3+ based on a carbon dot (C-dot)-aerogel hybrid prepared through in situ carbonization of 2-Thenoyltrifluoroacetone (TTA), a high-affinity heavy metal chelator. The TTA-C-dot-aerogel enabled the detection of UO2 2+ ions, which induced a significant red fluorescence shift, whereas Eu3+ and particularly Sm3+ ions gave rise to pronounced fluorescence quenching. Importantly, the lanthanide/actinide ion-selective TTA-C-dots could be synthesized only in situ inside the aerogel pores, indicating the crucial role of the aerogel host matrix both in enabling the formation of the C-dots and in promoting the adsorption and interactions of the lanthanide and actinide metal ions with the embedded C-dots.
Solvent extraction of gallium(III) with 2-Thenoyltrifluoroacetone
Talanta 1976 Jan;23(1):51-3.PMID:18961800DOI:10.1016/0039-9140(76)80011-2.
Gallium can be quantitatively extracted at trace levels with 2-Thenoyltrifluoroacetone in xylene at pH 4.5-6.0. Gallium is determined in the organic phase photometrically by complexation with Rhodamine B. The system conforms to Beer's law (at 565 nm) in the concentration range 2-59 mug ml . The complex is stable for 24 hr. Salting-out agents have no effect on the extraction. Gallium can be extracted and determined in a single extraction in presence of many elements associated with it, such as indium, thallium and aluminium.
Europium(III) Complex-Functionalized SiO2@mTiO2 Nanospheres for Al3+-Modulated Multicolor Emission
Nanomaterials (Basel) 2021 Oct 28;11(11):2886.PMID:34835650DOI:10.3390/nano11112886.
A europium(III) hybrid material Eu(tta)3bpdc-SiO2@mTiO2 (Htta = 2-Thenoyltrifluoroacetone, H2bpdc = 2,2'-bipyridine-3,3'-dicarboxylic acid) was successfully designed and synthesized by the covalent grafting complex Eu(tta)3bpdc to SiO2@mTiO2 core-shell nanosphere. The FT-IR, PXRD, XPS, TEM, HRTEM, SAED, TGA and PL were performed to characterize these materials. The results indicate that core-shell nanosphere structure and anatase crystallites of SiO2@mTiO2 are retained well after grafting the europium complex. Hybrid material Eu(tta)3bpdc-SiO2@mTiO2 displays uniform nanosphere structure, bright red color and long lifetime, which can serve as a multicolor emission material modulated by using Al3+ ions via the cation exchange approach under a single-wavelength excitation. To the best of our knowledge, this work is the first multicolor emissive sensor for Al3+ ions based on the lanthanide hybrid material.
Surfactant-assisted emulsification dispersive liquid-liquid microextraction using 2-Thenoyltrifluoroacetone as a chelating agent coupled with electrothermal atomic absorption spectrometry for the speciation of chromium in water and rice samples
Food Chem 2018 Apr 25;246:379-385.PMID:29291862DOI:10.1016/j.foodchem.2017.11.050.
A novel method was developed by SAE-DLLME for chromium speciation in water and rice samples using 2-Thenoyltrifluoroacetone (TTA) as a chelating reagent by ETAAS. The speciation of Cr(III) and Cr(VI) was achieved by complexation of Cr(III)-TTA and the total Cr was measured after reduction of Cr(VI) to Cr. The calibration graph was linear in the range of 0.02-2.50 µg L-1, with a detection limit of 0.0052 µg L-1. The %RSD was in range of 2.90-3.30% at 0.5, 1.5 and 2.5 µg L-1 of Cr(III), n = 5 and the EF was 54.47. The method was applied to chromium speciation and total chromium determination in real samples and gave recoveries in the range of 96.2-103.5% and 97.1-102.7% for Cr(III) and Cr(VI) in water samples and 93.7-103.5% of total Cr in rice samples. The accuracy of the method was evaluated by analysis of SRM 1573a with good agreement compared to the certified value.
Synthesis and photoluminescence properties of silica-modified SiO2@ANA-Si-Tb@SiO2, SiO2@ANA-Si-Tb-L@SiO2 core-shell-shell nanostructured composites
R Soc Open Sci 2019 Aug 7;6(8):190182.PMID:31598231DOI:10.1098/rsos.190182.
Three novel core-shell nanostructured composites SiO2@ANA-Si-Tb, SiO2@ANA-Si-Tb-L (L = second ligand) with SiO2 as the core and terbium organic complex as the shell were successfully synthesized. The core and shell were connected together by covalent bonds. The terbium ion was coordinated with organic ligand-forming terbium organic complex in the shell layer. The organosilane (HOOCC5H4NN(CONH(CH2)3Si(OCH2CH3)3)2 (abbreviated as ANA-Si) was used as the first ligand and 1,10-phenanthroline (phen) or 2-Thenoyltrifluoroacetone (TTA) was used as the second ligand. Furthermore, silica-modified SiO2@ANA-Si-Tb@SiO2, SiO2@ANA-Si-Tb-L@SiO2 core-shell-shell nanostructured composites were also synthesized by sol-gel chemical route, which involved the hydrolysis and polycondensation processes of tetraethoxysilane (TEOS) using cetyltrimethyl ammonium bromide (CTAB) as a surface-active agent. An amorphous silica shell was coated around the SiO2@ANA-Si-Tb, SiO2@ANA-Si-Tb-L core-shell nanostructured composites. The core-shell and core-shell-shell nanostructured composites exhibited excellent luminescence in the solid state. Meanwhile, an improved luminescent stability property of the core-shell-shell nanostructured composites was observed for the aqueous solution. This type of core-shell-shell nanostructured composites exhibited bright luminescence, high stability and good solubility, which may present potential applications in the fields of optoelectronic devices, bio-imaging, medical diagnosis and study on the structure of function composite materials.