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6804-07-5

中文名稱 卡巴多
英文名稱 Carbadox
CAS 6804-07-5
分子式 C11H10N4O4
分子量 262.22
MOL 文件 6804-07-5.mol
更新日期 2025/01/06 14:51:16
6804-07-5 結(jié)構(gòu)式 6804-07-5 結(jié)構(gòu)式

基本信息

中文別名
痢立清
喹肼脂
卡巴得
卡巴氧
卡巴多
卡巴多司
2(2-喹啉基-1,1-亞甲基)肼基甲酸甲酯
N,N’-二氧化甲基(2-喹喔啉基亞甲基)肼羧酸酯
2-(喹喔啉-2-亞甲基)肼-羧酸甲酯-N,N'-二氧化物
英文別名
CBX
M31
MOD1
gs6244
Mecadox
CARBADO
p25beta
getroxel
fortigro
karbadox
所屬類別
分析化學(xué):生命科學(xué)標(biāo)準(zhǔn)品

物理化學(xué)性質(zhì)

熔點(diǎn)239-240°C
沸點(diǎn)405.47°C (rough estimate)
密度1.3602 (rough estimate)
折射率1.6000 (estimate)
閃點(diǎn)18°(64°F)
儲存條件2-8°C
溶解度DMSO(輕微超聲處理)
酸度系數(shù)(pKa)10.51±0.46(Predicted)
形態(tài)粉末
顏色黃色至深黃色
水溶解性Soluble in 1N NaOH (50 mg/ml), and water (partly).
穩(wěn)定性感光
CAS 數(shù)據(jù)庫6804-07-5

安全數(shù)據(jù)

危險性符號(GHS)GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07,GHS08
警示詞危險
危險性描述H228-H302-H350
危險品標(biāo)志F,T
危險類別碼45-11-22
安全說明53-45
危險品運(yùn)輸編號UN 1325 4.1/PG 2
WGK Germany3
RTECS號FE2779000
危險等級4.1
海關(guān)編碼29339900
毒害物質(zhì)數(shù)據(jù)6804-07-5(Hazardous Substances Data)

應(yīng)用領(lǐng)域

用途1
用作藥用輔料、飼料添加劑
卡巴多價格(試劑級)
報價日期產(chǎn)品編號產(chǎn)品名稱CAS號包裝價格
2024/11/08HY-B1340卡巴多
Carbadox
6804-07-5100mg400元
2024/11/08HY-B1340卡巴多
Carbadox
6804-07-510mM * 1mLin DMSO440元

常見問題列表

生物活性
Carbadox 是一種喹喔啉二氧化氮抗生素化合物,廣泛用于育齡期的豬,以控制腸道疾病,提高飼料利用率。
靶點(diǎn)

Bacterial

體外研究

The results of MTT assay demonstrate a dose-dependent decrease in mitochondrial activity in Vero cells at all concentrations of Carbadox. Treatment with Carbadox at the highest concentration of 160 μg/mL results in cell viability down to only 12%. Cells following Carbadox treatment show a dose-dependent increase of the DNA migration (p<0.01). The nuclear division index (NDI) reduces markedly with the increase doses of Carbadox.

體內(nèi)研究

Alpha diversities (Shannon diversity, Heips evenness, and inverse Simpson indices) of samples from medicated piglets compare to non-medicated piglets are significantly different at 2, 3, and 4 days after continuous Carbadox, but not different in either late Carbadox or at any time during the withdrawal period. Analysis of the community structure of bacteria in animals shows significant differences at days 3 and 4 of early Carbadox treatment ([R=0.32, p=0.015] and [R=0.54, p=0.003], respectively), but not before starting antibiotic treatment (p=0.82). No significant differences in E. coli colony forming units (CFUs) are observed during the Carbadox-treatment period of the study or late in the withdrawal period. E. coli CFUs are significantly different between the medicated and non-medicated groups on day 2 after the withdrawal of Carbadox.

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