Epioxytetracycline
(Synonyms: 差向土霉素) 目录号 : GC41326
A degradation product of oxytetracycline
Cas No.:14206-58-7
Sample solution is provided at 25 µL, 10mM.
;)
,-1-7$$$37316672.jpg');)
;)
;)
$$$36806353.jpg');)
;33(7)%EF%BC%9A546-561$$$37156877.jpg');)
;)
;)
;)
%201124-1138.$$$35908550.jpg');)
%20766-780.$$$37100057.jpg');)
%20418-432.$$$36893736.jpg');)
%EF%BC%9A-240-255.$$$35108512.jpg');)
533-545$$$36543525.jpg');)
%201-13.$$$36600053.jpg');)
;)
Quality Control & SDS
- View current batch:
- Purity: >99.00%
- COA (Certificate Of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Epioxytetracycline is a degradation product of the antibiotic oxytetracycline . It has been found in swine manure compost and wastewater and is considered a pollutant.
| Cas No. | 14206-58-7 | SDF | |
| 别名 | 差向土霉素 | ||
| Canonical SMILES | O=C1C2=C(O)C=CC=C2[C@](O)(C)[C@]3([H])C1=C(O)[C@@](C(C(C(N)=O)=C(O)[C@@H]4N(C)C)=O)(O)[C@@]4([H])[C@H]3O | ||
| 分子式 | C22H24N2O9 | 分子量 | 460.4 |
| 溶解度 | DMSO: slightly soluble,Methanol: slightly, heated | 储存条件 | Store at -20°C,protect from light |
| 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。 |
||
| 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 | |||
 |
1 mg | 5 mg | 10 mg |
| 1 mM | 2.172 mL | 10.8601 mL | 21.7202 mL |
| 5 mM | 0.4344 mL | 2.172 mL | 4.344 mL |
| 10 mM | 0.2172 mL | 1.086 mL | 2.172 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。
Biochar accelerates the removal of tetracyclines and their intermediates by altering soil properties
J Hazard Mater 2019 Dec 15;380:120821.PMID:31326833DOI:10.1016/j.jhazmat.2019.120821.
Tetracyclines accumulation in soil environment potentially threatens agroecosystem safety. Interestingly, biochar could clean up organic pollutants, but to what extent biochar affects the removal of tetracyclines is unknown. To investigate it, five types of biochars derived from cow manure (CMB) and other four plant materials were respectively added into soils contaminated with a mixture of tetracycline, oxytetracycline, and chlortetracycline for 60-day incubation in the dark. Three parent tetracyclines and their corresponding intermediates (epitetracycline, anhydrotetracycline, epianhydrotetracycline, Epioxytetracycline, epichlortetracycline, and demethylchlortetracycline) were respectively determined and named as TTCs, OTCs and CTCs. Obtained results showed biochar especially CMB could effectively remove the antibiotics (P < 0.05). Compared to control, the removal rate of TTCs, OTCs and CTCs respectively increased by up to 10.86%, 10.29% and 10.12% in CMB-added soil. The increased removal rate of the antibiotics after biochar addition was due to the increasing accessibilities for degrading microorganisms via the elevating electrical conductivity. Moreover, biochar addition might stimulate these microbial activities through the increase of C and N supplement. Our results indicate biochar accelerates the removal of tetracyclines and their intermediates by altering soil properties and thus increasing the antibiotics accessibilities, which provide insights into how biochar accelerates the removal for these antibiotics.
[Distribution and Treatment of Antibiotics in Typical WWTPs in Small Towns in China]
Huan Jing Ke Xue 2018 Jun 8;39(6):2724-2731.PMID:29965628DOI:10.13227/j.hjkx.201710104.
As a new, persistent pollutant in the environment, antibiotics are one of the most important pollutants in sewage treatment plants. The objective of this work was to investigate the concentration distribution and removal efficiency of antibiotics for three typical wastewater treatment technologies applied in small towns (CASS, A2/O, and Orbal oxidation ditch) using solid phase extraction-liquid chromatography-tandem mass spectrometry. Sixteen typical antibiotics, including four tetracyclines, three β-lactams, four macrolides, three quinolones, and two sulfonamides, were analyzed in the influent and effluent. In addition, the relationship between the presence of antibiotics and the basic water quality (NH4+-N, TN, COD, pH, etc.) in the WWTPs was analyzed. The results showed that ofloxacin (OFX) and norfloxacin (NOR) were the main antibiotics in the WWTPs in this study. However, the concentrations of these two antibiotics in the effluent were low, indicating effective antibiotic removal efficiency. The antibiotic removal efficiency was higher than 60% in five of the WWTPs. Compared with the A2/O process, the CASS and Orbal oxidation ditch technologies resulted in higher removals of most of the antibiotics. In addition, the CASS and A2/O processes worked best for the removal of β-lactam [ampicillin (AMP) and penicillin (PCN)], quinolones (ENR, NOR, and OFX), and macrolide (CLR), while the Orbal oxidation ditch worked best for the removal of tetracyclines (TC and OTC) and sulfonamides [sulfadiazine (SD)]. The correlation between antibiotic concentration and the basic parameters of water quality (NH4+-N, TN, COD, pH, etc.) was analyzed, and it was found that the water quality parameters had some effect on the concentration of antibiotics. With higher concentrations of the basic water quality parameters, higher the concentration of erythromycin (EM), roxithromycin (ROX), 4-epi-Tetracycline (E-TC), clarithromycin (CLR), ciprofloxacin (CIP), ofloxacin (OFX), Epioxytetracycline (E-OTC), tetracyclines (TC), oxytetracycline (OTC), and norfloxacin (NOR) were observed. In summary, it is important to ensure the stable operation of small town WWTPs to reduce the ecological risk of antibiotics.
Determination of oxytetracycline in premixes and veterinary products by liquid chromatography
J Assoc Off Anal Chem 1986 Jan-Feb;69(1):28-30.PMID:3949693doi
A liquid chromatographic method for the assay of oxytetracycline in premixes and veterinary products is described. Premix samples are extracted with acidified methanol, diluted with mobile phase, and filtered before chromatography on a C-8, reverse phase column. The assay method separates oxytetracycline from Epioxytetracycline, tetracycline, and chlortetracycline. Total elution time for oxytetracycline is less than 5 min at 1.5 mL/min. Five spiked premix samples each of 2 and 50 g/lb had a coefficient of variation of 3.5 and 4.5% and a mean recovery of 99 and 104%, respectively. The results of premixes and veterinary products assayed by this method compared closely with those of the same assayed by the official AOAC microbiological method.