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Propargyl-3-sulfopropyl ether sodium salt
- русский язык имя
- английское имяPropargyl-3-sulfopropyl ether sodium salt
- CAS №30290-53-0
- CBNumberCB9228896
- ФормулаC6H11NaO4S
- мольный вес202.2
- EINECS608-454-7
- номер MDLMFCD00798857
- файл Mol30290-53-0.mol
химическое свойство
плотность | 1.21 at 20℃ |
давление пара | 0-2992.94Pa at 25℃ |
форма | Liquid |
InChI | InChI=1S/C6H10O4S.Na.H/c1-2-4-10-5-3-6-11(7,8)9;;/h1H,3-6H2,(H,7,8,9);; |
ИнЧИКей | QZGFGSLFVLDKEY-UHFFFAOYSA-N |
SMILES | C(S(O)(=O)=O)CCOCC#C.[NaH] |
LogP | -4.1 |
Surface tension | 72.53-72.79mN/m at 1g/L and 19.9℃ |
рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H315:При попадании на кожу вызывает раздражение.
H319:При попадании в глаза вызывает выраженное раздражение.
H335:Может вызывать раздражение верхних дыхательных путей.
H302:Вредно при проглатывании.
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оператор предупредительных мер
P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.
P305+P351+P338:ПРИ ПОПАДАНИИ В ГЛАЗА: Осторожно промыть глаза водой в течение нескольких минут. Снять контактные линзы, если Вы ими пользуетесь и если это легко сделать. Продолжить промывание глаз.
Propargyl-3-sulfopropyl ether sodium salt химические свойства, назначение, производство
Описание
Propargyl-3-sulfopropyl ether sodium salt is a sulfonate used as a co-brightener with glycerol in the electroplating industry. It is also used as an alkaline industrial chemical that can be used to remove tellurium from glass and ceramics. Propargyl-3-sulfopropyl ether sodium salt is prepared by reacting propargyl alcohol with sodium sulfite and ethylene diamine. This reaction produces propargyl sulfonic acid, which reacts with ethylene oxide to form the desired product.Использование
Propargyl-3-sulfopropyl ether sodium salt is a sulfonate used as a co-brightener with glycerol in the electroplating industry. It is also used as an alkaline industrial chemical for removing tellurium from glass and ceramics.Синтез
Propargyl-3-sulfopropyl ether sodium salt is prepared by the reaction of 1,3-propanesultone and propargyl alcohol. The specific synthesis steps are as follows:To a chilled (5 °C) slurry of NaH (60% in mineral oil, 1.60 g, 40.9 mmol, 1.0 equiv.) in dry DMF (30 mL) was added dropwise a solution of propargyl alcohol (2.4 mL, 40.9 mmol, 1.0 equiv.) in dry DMF (30 mL) over a ten minute period. I ,3-Propanesultone (5.0 g, 40.9 minol, 1.0 equiv.) was dissolved in dry DMF (30mL), and the resulting solution added dropwise over a five minute period to the chilled sodium propargylate solution. After stirring for ten minutes in the ice bath, the flask was transferred to an oil bath and heated at 60°C for three hours. Most of the DMF was then removed by rotavap, and the remaining oil was triturated with 200 mL diethyl ether to yield a white solid, which was collected by vacuum filtration. The product was driedunder vacuum to provide Propargyl-3-sulfopropyl ether sodium salt as a white powder (7.4 g, 90%).
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