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CAS RN: 563-41-7 | 產(chǎn)品編碼: S0032
Semicarbazide Hydrochloride
純度/分析方法: >99.0%(T)
別名:
- 鹽酸氨基脲
- 肼甲酰胺鹽酸鹽
- 氨基脲鹽酸鹽
- 鹽酸氨基甲酰肼
產(chǎn)品文檔:
規(guī)格 | 單價(jià) | 上海 | 天津 | 日本* | 數(shù)量 | 庫(kù)存詳情 |
---|---|---|---|---|---|---|
25G |
¥170.00
|
4 | 1 | 25 |
|
|
100G |
¥350.00
|
一個(gè)工作日后發(fā)貨 | 一個(gè)工作日后從上海發(fā)貨 | 請(qǐng)聯(lián)系我們 |
|
|
500G |
¥640.00
|
3 | 2 | ≥100 |
|
* 點(diǎn)擊“查詢”可查看預(yù)計(jì)發(fā)貨日期,僅供參考。
* 無(wú)具體發(fā)貨日期的情況,如:顯示“8個(gè)工作日后發(fā)貨”,將在您訂購(gòu)日起的8個(gè)工作日后發(fā)貨。
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* 對(duì)于可分裝產(chǎn)品,11:30前的訂單,當(dāng)天發(fā)貨;11:30后的訂單,隔天發(fā)貨。
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* 更多信息,請(qǐng)聯(lián)系營(yíng)業(yè)部:021-67121386 / Sales-CN@TCIchemicals.com 。任何貨期、規(guī)格或包裝方面的需求,請(qǐng)聯(lián)系我們 。
* 無(wú)具體發(fā)貨日期的情況,如:顯示“8個(gè)工作日后發(fā)貨”,將在您訂購(gòu)日起的8個(gè)工作日后發(fā)貨。
* 我們將以最優(yōu)方式從上海/天津兩大倉(cāng)庫(kù)發(fā)貨。國(guó)內(nèi)庫(kù)存不足,需兩周左右向日本總部調(diào)貨。
* 對(duì)于可分裝產(chǎn)品,11:30前的訂單,當(dāng)天發(fā)貨;11:30后的訂單,隔天發(fā)貨。
* 如需大包裝,請(qǐng)點(diǎn)擊“大包裝詢價(jià)”按鈕(對(duì)于某些產(chǎn)品我們無(wú)法提供大包裝)。
* TCI會(huì)經(jīng)常復(fù)審儲(chǔ)藏條件以對(duì)其進(jìn)行優(yōu)化,請(qǐng)以在線目錄為準(zhǔn),敬請(qǐng)留意。
* 更多信息,請(qǐng)聯(lián)系營(yíng)業(yè)部:021-67121386 / Sales-CN@TCIchemicals.com 。任何貨期、規(guī)格或包裝方面的需求,請(qǐng)聯(lián)系我們 。
技術(shù)規(guī)格
Appearance | White to Almost white powder to crystal |
Purity(Bromination Method) | min. 99.0 % |
物性(參考值)
溶解性(微溶于) | 醇 |
溶解性(不溶于) | 乙醚 |
GHS
象形圖 | |
信號(hào)詞 | 危險(xiǎn) |
危險(xiǎn)性說(shuō)明 | H301 : 吞咽會(huì)中毒。 H315 : 造成皮膚刺激。 H319 : 造成嚴(yán)重眼刺激。 H361 : 懷疑對(duì)生育能力或胎兒造成傷害。 H373 : 長(zhǎng)期或反復(fù)接觸可能損害器官。 |
防范說(shuō)明 | P501 : 將內(nèi)裝物/容器送到批準(zhǔn)的廢物處理廠處理。 P260 : 不要吸入粉塵/ 煙/ 氣體/ 煙霧/ 蒸氣/ 噴霧。 P270 : 使用本產(chǎn)品時(shí)不要進(jìn)食、飲水或吸煙。 P202 : 在閱讀并明了所有安全措施前切勿搬動(dòng)。 P201 : 使用前取得專(zhuān)用說(shuō)明。 P264 : 作業(yè)后徹底清洗皮膚。 P280 : 戴防護(hù)手套/穿防護(hù)服/戴防護(hù)眼罩/戴防護(hù)面具。 P302 + P352 : 如皮膚沾染:用水充分清洗。 P308 + P313 : 如接觸到或有疑慮:求醫(yī)/就診。 P337 + P313 : 如仍覺(jué)眼刺激:求醫(yī)/就診。 P305 + P351 + P338 : 如進(jìn)入眼睛:用水小心沖洗幾分鐘。如戴隱形眼鏡并可方便地取出,取出隱形眼鏡。繼續(xù)沖洗。 P362+P364 : 脫掉沾污的衣服,清洗后方可重新使用。 P332 + P313 : 如發(fā)生皮膚刺激:求醫(yī)/就診。 P301 + P310 + P330 : 如誤吞咽:立即呼叫急救中心/醫(yī)生。漱口。 P405 : 存放處須加鎖。 |
相關(guān)法規(guī)
RTECS# | VT3500000 |
運(yùn)輸信息
UN編號(hào) | UN2811 |
類(lèi)別 | 6.1 |
包裝類(lèi)別 | III |
監(jiān)管條件代碼(*) |
應(yīng)用
Synthesis of Alkynyl Ketones using Eschenmoser-Tanabe Fragmentation(alternative method)
Typical Procedure:
To a stirred solution of semicarbazide hydrochloride (12.94 g, 116.0 mmol) and sodium acetate trihydrate (0.95 g, 12 mmol) in water (116 mL) is added 1 (2.63 g, 11.6 mmol) at room temperature. Sufficient 95% ethanol is added to bring about a homogenous solution. After stirring at room temperature for 7 h, the reaction mixture is extracted with ethyl acetate. The combined organic phases are washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product is purified by silica gel chromatography (ethyl acetate → ethyl acetate : methanol = 9 : 1) to give 2 (2.92 g, 89%) as a white solid.
Next, to a stirred solution of 2 (1.86 g, 6.57 mmol) in dichloromethane (65.7 mL) is added portionwise 95% lead tetraacetate (6.42 g, 13.8 mmol), maintaining the bath temperature at –10 °C After stirring for 1 h at –10 °C, ethyl acetate is added to the reaction mixture, which is allowed to warm to room temperature. Then the mixture is filtered through a Celite pad and concentrated under reduced pressure. The crude product is purified by silica gel column chromatography (hexane : ethyl acetate = 4 : 1) to give 3 (0.83 g, 60%) as a colorless oil.
To a stirred solution of semicarbazide hydrochloride (12.94 g, 116.0 mmol) and sodium acetate trihydrate (0.95 g, 12 mmol) in water (116 mL) is added 1 (2.63 g, 11.6 mmol) at room temperature. Sufficient 95% ethanol is added to bring about a homogenous solution. After stirring at room temperature for 7 h, the reaction mixture is extracted with ethyl acetate. The combined organic phases are washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product is purified by silica gel chromatography (ethyl acetate → ethyl acetate : methanol = 9 : 1) to give 2 (2.92 g, 89%) as a white solid.
Next, to a stirred solution of 2 (1.86 g, 6.57 mmol) in dichloromethane (65.7 mL) is added portionwise 95% lead tetraacetate (6.42 g, 13.8 mmol), maintaining the bath temperature at –10 °C After stirring for 1 h at –10 °C, ethyl acetate is added to the reaction mixture, which is allowed to warm to room temperature. Then the mixture is filtered through a Celite pad and concentrated under reduced pressure. The crude product is purified by silica gel column chromatography (hexane : ethyl acetate = 4 : 1) to give 3 (0.83 g, 60%) as a colorless oil.
References
- 1)Thermolysis of Δ3-1 ,3,4-oxadiazolin-2-ones and 2-phenylimino-Δ3-l,3,4-oxadiazolinesderived from α,β-epoxyketones. An alternative method for the conversion of α,β-epoxyketones to alkynones and alkynals
- 2)Total Synthesis of (–)-Mersicarpine
參考文獻(xiàn)
產(chǎn)品文檔 (部分產(chǎn)品的分析圖譜無(wú)法提供,敬請(qǐng)諒解。)
化學(xué)品安全說(shuō)明書(shū)(SDS)
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技術(shù)規(guī)格
CoA及其他文檔
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示例 CoA
可下載CoA示例。注:該示例不一定是最新批次的CoA。
目前沒(méi)有該產(chǎn)品的 CoA?示例。
分析圖譜
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