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9-гидроксиxантен
- английское имя9-Hydroxyxanthene
- CAS №90-46-0
- CBNumberCB6298513
- ФормулаC13H10O2
- мольный вес198.22
- EINECS201-996-1
- номер MDLMFCD00005057
- файл Mol90-46-0.mol
Температура плавления | 122-124 °C |
Температура кипения | 275.53°C (rough estimate) |
плотность | 0.83 g/mL at 20 °C |
показатель преломления | 1.6620 (estimate) |
Fp | 11 °C |
температура хранения | 2-8°C |
растворимость | methanol: 0.1 g/mL, clear |
форма | Crystalline Powder |
пка | 13.57±0.20(Predicted) |
цвет | White to off-white |
Чувствительный | Light Sensitive |
БРН | 10395 |
Стабильность | Stable. Combustible. Incompatible with strong oxidizing agents. |
LogP | 2.270 (est) |
Справочник по базе данных CAS | 90-46-0(CAS DataBase Reference) |
Рейтинг продуктов питания EWG | 1 |
FDA UNII | 7131M69IKF |
Система регистрации веществ EPA | 9H-Xanthen-9-ol (90-46-0) |
UNSPSC Code | 12352100 |
NACRES | NA.22 |
Коды опасности | F,T,Xi,Xn | |||||||||
Заявления о рисках | 11-23/24/25-39/23/24/25-40 | |||||||||
Заявления о безопасности | 7-16-24-45-24/25-36-22-36/37 | |||||||||
РИДАДР | UN 1230 3/PG 2 | |||||||||
WGK Германия | 3 | |||||||||
RTECS | ZD5710000 | |||||||||
F | 8-10-23 | |||||||||
Примечание об опасности | Irritant | |||||||||
TSCA | Yes | |||||||||
кода HS | 29329990 | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
опасность
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вредная бумага
H301+H311+H331:Токсично при проглатывании, при контакте с кожей или при вдыхании.
H225:Легковоспламеняющаяся жидкость. Пары образуют с воздухом взрывоопасные смеси.
H370:Поражает органы (Глаза) в результате однократного воздействия.
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оператор предупредительных мер
P210:Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.
P280:Использовать перчатки/ средства защиты глаз/ лица.
P301+P310+P330:ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.
P302+P352+P312:ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды. Обратиться за медицинской помощью при плохом самочувствии.
P304+P340+P311:ПРИ ВДЫХАНИИ: Свежий воздух, покой. Обратиться за медицинской помощью.
9-гидроксиxантен химические свойства, назначение, производство
Химические свойства
White needle crystals. Melting point 123℃, easily soluble in cold acetone, soluble in alcohol, chloroform, very slightly soluble in water. Dissolved in concentrated sulfuric acid, it is yellow and has green fluorescence.Использование
9-Hydroxyxanthene is an Intermediate in the preparation of Propantheline Bromide. It is useful in tests for urea also used in the protection of thiols as their S-xanthenyl (Xan) thioethers, by reaction in the presence of TFA.прикладной
Xanthydrol may be used as a derivatization agent for the following:Analysis of urea in urine and wine samples using high-performance liquid chromatography (HPLC) technique.
Analysis of trace levels of carbamate pesticides in surface water by gas chromatography–mass spectrometry (GC-MS).
Определение
9H-Xanthen-9-ol is a derivative of xanthene that is a natural product found in Xanthium spinosum and Xanthium strumarium.Подготовка
synthesis of xanthydrol: The amalgam sodium in dry toluene was warmed to 50°C, the xanthone-ethanol suspension was added, and the temperature was rapidly raised to 60-70°C with vigorous stirring. After the reaction is completed, the mercury is separated. The reaction solution was filtered, the filtrate was poured into the stirred blue distilled water, the 9-hydroxyxanthene was filtered out, washed with water, and dried to obtain the finished product with a yield of 91-95%.Реакции
9-Hydroxyxanthene (xanthydrol) reacts with a variety of proteins and inactivates certain enzymes. The research data indicate that in acetic acid solution xanthydrol reacts with the following amino acids: arginine, asparagine, cysteine, glutamine, histidine, lysine, and tryptophan. The a-amino group of cu-amino acids does not react with xanthydrol under these conditions, since alanine, serine, isoleucinc, and tyrosine failed to react[1]. This compound could help to increase extraction efficiency, because it could react with ethyl carbamate to form low-polar product, which facilitated transfer ethyl carbamate into organic phase[2].Общее описание
Xanthydrol is also known as 9H-xanthen-9-ol. Xanthydrol is a natural drug that has been used in traditional Chinese medicine for treating a variety of diseases. It is extracted from Rhizoma Gastrodiae and Angelicae Dahuricae. It has shown to be effective against various metabolic disorders, including insulin resistance, hyperlipidemia, and diabetes. The mechanism of action of Xanthydrol is not known but it is thought to be due to its ability to activate the immune system by transferring reactions and promoting the production of antibodies. It also shows anti-inflammatory effects by inhibiting the production of prostaglandins and leukotrienes. It can also inhibit angiotensin II, which may reduce high blood pressure and congestive heart failure.Методы очистки
Crystallise xanthydrol from EtOH and dry it at 40-50o. [Beilstein 17 H 129, 17 I 72, 17 II 146, 17 III/IV 1602, 17/4 V 502.]9-гидроксиxантен запасные части и сырье
9-гидроксиxантен поставщик
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