Acid orange 7
(Synonyms: 酸性橙7,Orange II; D&C Orange NO. 4) 目录号 : GC60559
Acid orange 7 (2-naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA C015) is an azo dye used for dyeing wool.
Cas No.:633-96-5
Sample solution is provided at 25 µL, 10mM.
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Quality Control & SDS
- View current batch:
- Purity: >98.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Acid orange 7 (2-naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA C015) is an azo dye used for dyeing wool.
| Cas No. | 633-96-5 | SDF | |
| 别名 | 酸性橙7,Orange II; D&C Orange NO. 4 | ||
| Canonical SMILES | O=S(C1=CC=C(/N=N/C2=C3C=CC=CC3=CC=C2O)C=C1)(O[Na])=O | ||
| 分子式 | C16H11N2NaO4S | 分子量 | 350.32 |
| 溶解度 | Water: 25 mg/mL (71.36 mM) | 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 | 2.8545 mL | 14.2727 mL | 28.5453 mL |
| 5 mM | 0.5709 mL | 2.8545 mL | 5.7091 mL |
| 10 mM | 0.2855 mL | 1.4273 mL | 2.8545 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。
Decolorization of Acid orange 7 by extreme-thermophilic mixed culture
Bioresour Technol 2019 Nov;291:121875.PMID:31362846DOI:10.1016/j.biortech.2019.121875.
Although a large amount of textile wastewater is discharged at high temperatures, azo dye reduction under extreme-thermophilic conditions by mixed cultures has gained little attention. In this study, Acid orange 7 (AO7) was used as the model azo dye to demonstrate the decolorization ability of an extreme-thermophilic mixed culture. The results showed that a decolorization efficiency of over 90% was achieved for AO7. The neutral red (NR, 0.1 mM) could promote AO7 decolorization, in which the group of Cell + NR offered the highest decolorization rate of 1.568 1/h and t1/2 was only 0.44 h, whereas after CuCl2 addition, the decolorization rate (0.141 1/h) was lower and t1/2 (4.92 h) was much longer. Thus, CuCl2 notably inhibited this process. Caldanaerobacter (64.0%) and Pseudomonas (25.4%) were the main enriched bacteria, which were not reported to have the ability for dye decolorization. Therefore, this study extends the application of extreme-thermophilic biotechnology.
Study on the catalytic degradation of Acid orange 7 and the potential mechanism by ferrous-percarbonate
Water Environ Res 2022 Oct;94(10):e10796.PMID:36278310DOI:10.1002/wer.10796.
Factors affecting the degradation of Acid orange 7 (AO7) were evaluated and optimized when ferrous was used to catalyze percarbonate in the present study. The optimized conditions included the initial pH values ranging from 3 to 11 for AO7 solution, the initial level of AO7, sodium percarbonate (SPC), and Fe2+ . Some ions and natural organic materials, which commonly exist in natural water, were also tested to evaluate their potential impacts on the degradation of AO7. The degradation efficiency of AO7 was up to 95% under the optimized test conditions, where the ferrous/percarbonate/AO7 molar ratio was 15/10/1 in the 0.285 mmol/l AO7 aqueous solution. The presence of Cl- , SO4 2- , NO3 - , Na+ , and Mg2+ did not affect the removal of AO7. The addition of HCO3 - significantly inhibited its removal, even when the concentration of HCO3 - was low to 0.6 mmol/l. A slight inhibition effect was observed when the added concentration of humic acid ranged from 0.5 to 5 mg/l, whereas the residue of AO7 was significantly enhanced when the level of humic acid was continually increased from 50 to 100 mg/l. Hydroxyl radicals (•OH) were the main reactive intermediates controlling the oxidation of AO7 in the present Fe2+ /SPC system. The produced intermediates through the degradation of AO7 were identified to include 2-coumaranone, 2-naphthol, phthalic acid, phthalimide, N-methylnaphthylamine, and 2-methylphenol. The proposed degradation pathways are consistent with the radical formation and the identified intermediates. PRACTITIONER POINTS: The ferrous/percarbonate system can remove 95% of AO7 under the optimized conditions. AO7 removal was inhibited by adding HCO3 - and humic acid, but not affected by Cl- , SO4 2- , NO3 - , Na+ , and Mg2+ . Hydroxylation, ring opening, and mineralization driven by the generated hydroxyl radicals were derived as the major processes for degrading AO7.
Electrochemical oxidation of Acid orange 7 azo dye using a PbO2 electrode: Parameter optimization, reaction mechanism and toxicity evaluation
Chemosphere 2020 Feb;241:125010.PMID:31605993DOI:10.1016/j.chemosphere.2019.125010.
In this study, electrochemical oxidation of Acid orange 7 (AO 7) azo dye has been investigated using a Fe-doped PbO2 electrode. The degradation of AO 7 followed pseudo-first-order reaction kinetics. The removals of AO 7, chemical oxygen demand (COD) and total organic carbon (TOC) were 87.15%, 49.88% and 44.94% after 60 min of electrolysis at the optimal conditions (Na2SO4 concentration 0.1 M, initial pH 5, initial AO 7 concentration 100 mg L-1 and applied current density 20 mA cm-2), respectively. And the corresponding degradation rate constant was 0.035 min-1. The intermediates formed during electrochemical process were identified, and a possible degradation pathway was proposed, which was initiated by the oxidation of azo bond (-NN-), hydroxylation and substitution reaction of -NH2 and -SO3H under the attack of OH, and ended with the formation of mineralization products such as NH4+, NO3-, SO42-, CO2 and H2O. The toxicity of treated AO 7 solution towards Vibrio fischeri increased slightly at first and then rapidly reduced to non-toxicity with prolonging time. The results indicate that electrochemical oxidation of AO 7 using Fe-doped PbO2 electrode is a promising way.
Degradation of Acid orange 7 (AO7) by a bacterium strain Flavobacterium mizutaii L-15
Water Sci Technol 2020 Jul;82(2):266-272.PMID:32941168DOI:10.2166/wst.2020.127.
Acid orange 7 (AO7) is an azo dye widely used in the dyeing and direct printing industry. AO7 is an environmental pollutant because the cleavage of azo bonds produces aromatic amines, which are considered mutagenic and carcinogenic. Microbial degradation is one of the most effective methods to remove environmental pollutants. A bacterium strain L-15 was isolated from the wastewater treatment system of a dye manufacturer. This strain is capable of decolorizing AO7. The strain was identified as Flavobacterium mizutaii based on its morphological, physiological and biochemical characteristics, and the sequence of 16S rDNA. The AO7-degrading characteristics and the effects of culture condition on the degrading efficiency of the strain were investigated by shake-flask culturing. The optimal degradation condition of L-15 was 30 °C and pH 7.0. After culturing at 30 °C for 3 days with the initial AO7 concentration of 20 mg/L, the degradation rate of AO7 was 60.45%. The optimal salt concentration was lower than 2%.
Persulfate activation by ferrocene-based metal-organic framework microspheres for efficient oxidation of orange acid 7
Environ Sci Pollut Res Int 2022 May;29(23):34464-34474.PMID:35040067DOI:10.1007/s11356-022-18669-2.
Ferrocene-based metal-organic framework with different transition metals (M-Fc-MOFs, M = Fe, Mn, Co) was synthesized by a simple hydrothermal method and used as a heterogeneous catalyst for persulfate activation. The samples were characterized by X-ray diffraction, transmission electron microscopy, X-ray electron spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. Meanwhile, the influences of factors such as catalyst dosage, persulfate concentration, and pH on the degradation of Acid orange 7 (AO7) were studied in detail. The results showed that hollow cobalt-based ferrocenyl metal-organic framework microspheres (Co-Fc-MOFs) exhibited the best catalytic performance, which is closely related to the synergy of Fc/Fc+ and Co(II)/Co(III) cycles in persulfate activation. Free radical quenching studies indicated that both sulfate and hydroxyl appeared to contribute to the degradation of AO7.