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ТРИБУТИЛФОСФАТ

ТРИБУТИЛФОСФАТ структура
126-73-8
CAS №
126-73-8
Химическое название:
ТРИБУТИЛФОСФАТ
английское имя:
Tributyl phosphate
Синонимы:
TBP;TRI-N-BUTYL PHOSPHATE;tributyl;ANTIFOAM T;AURORA KA-1641;BUTYL PHOSPHATE;Tributylphosphat;mcs2495;Tributyle;celluphos4
CBNumber:
CB4187323
Формула:
C12H27O4P
молекулярный вес:
266.31
MOL File:
126-73-8.mol

ТРИБУТИЛФОСФАТ атрибут

Температура плавления: -79 °C (lit.)
Температура кипения: 180-183 °C/22 mmHg (lit.)
плотность: 0.979 g/mL at 25 °C (lit.)
плотность пара: 9.2 (vs air)
давление пара: 27 mm Hg ( 178 °C)
показатель преломления: n20/D 1.424(lit.)
Fp: 380 °F
температура хранения: Store below +30°C.
растворимость: вода: растворим 1 мл в 165 мл воды
форма: жидкость
цвет: Прозрачный
Запах: Без запаха
Вязкость: 3.8cs (20C)
Растворимость в воде: 0,6 г/100 мл
Мерк: 14,9618
БРН: 1710584
Пределы воздействия: TLV-TWA 2.18 mg/m3 (0.2 ppm) (ACGIH), 5 mg/m3 (OSHA and NIOSH); IDLH 1300 mg/m3 (120 ppm) (NIOSH).
Диэлектрическая постоянная: 6.5(20℃)
Стабильность:: Стабильный. Горючий. Несовместим с сильными окислителями. Может быть чувствительным к воде.
LogP: 4 at 20℃
Непрямые добавки, используемые в веществах, контактирующих с пищевыми продуктами: TRIBUTYL PHOSPHATE
FDA 21 CFR: 175.105
Справочник по базе данных CAS: 126-73-8(CAS DataBase Reference)
FDA UNII: 95UAS8YAF5
Справочник по химии NIST: Tri-n-butylphosphate(126-73-8)
Система регистрации веществ EPA: Tributyl phosphate (126-73-8)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xn,F
Заявления о рисках 22-38-40-62-48/20-36/37/38-11-20/22
Заявления о безопасности 36/37-46-45-36/37/39-16-53
РИДАДР UN 1208 3/PG 2
OEB B
OEL TWA: 0.2 ppm (2.5 mg/m3)
WGK Германия 2
RTECS TC7700000
Температура самовоспламенения 770 °F
TSCA Yes
кода HS 29190010
Банк данных об опасных веществах 126-73-8(Hazardous Substances Data)
Токсичность LD50 orally in rats: 3.0 g/kg (Smyth, Carpenter)
ИДЛА 30 ppm
символ(GHS) GHS hazard pictogramsGHS hazard pictograms
сигнальное слово Warning
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H302 Вредно при проглатывании. Острая токсичность, пероральная Категория 4 Предупреждение GHS hazard pictograms P264, P270, P301+P312, P330, P501
H315 При попадании на кожу вызывает раздражение. Разъедание/раздражение кожи Категория 2 Предупреждение GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H351 Предполагается, что данное вещество вызывает раковые заболевания. Канцерогенность Категория 2 Предупреждение P201, P202, P281, P308+P313, P405,P501
H412 Вредно для водных организмов с долгосрочными последствиями. Опасность для водной среды, долгосрочная опасность Категория 3 P273, P501
Внимание
P201 Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.
P202 Перед использованием ознакомиться с инструкциями по технике безопасности.
P273 Избегать попадания в окружающую среду.
P301+P312 ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P302+P352 ПРИ ПОПАДАНИИ НА КОЖУ: Промыть большим количеством воды.
P308+P313 ПРИ подозрении на возможность воздействия обратиться за медицинской помощью.

ТРИБУТИЛФОСФАТ MSDS


TBP

ТРИБУТИЛФОСФАТ химические свойства, назначение, производство

Описание

On decomposition, TBP releases COx, toxic fumes of phosphoric acid, phosphorus oxides, and/or phosphine. TBP is incompatible with strong oxidising agents and alkalis. The major uses of TBP in industry are as a component of aircraft hydraulic fluid and as a solvent for rare earth extraction and purification. Minor uses of TBP include use as a defoamer additive in cement casings for oil wells, an anti-air entrainment additive for coatings and floor finishes, as well as a carrier for fluorescent dyes. The major uses of TBP comprise over 80% of the volume produced.

Химические свойства

Stable, colorless liquid; odorless. Miscible with most solvents and diluents; soluble in water. Combustible.

Физические свойства

Clear, colorless to pale yellow, odorless, slightly flammable, oily liquid

Использование

Tributyl phosphate is used as an antifoaming agent; plasticizer for cellulose esters, lacquers, plastic, and vinyl resins; component in hydraulic fluids for aircraft control systems.

Методы производства

Prepared by the reaction of phosphorus oxychloride with butyl alcohol.

Определение

ChEBI: A trialkyl phosphate that is the tributyl ester of phosphoric acid.

Общее описание

Tributyl phosphate is an organophosphorus compound, which is widely used as a flame retardant and plasticizer in a variety of industrial products.

Реакции воздуха и воды

Water insoluble. Reacts slowly with water under basic conditions.

Профиль реактивности

Tributyl phosphate is incompatible with strong oxidizing agents and strong bases. Attacks some forms of plastics and rubber .

Угроза здоровью

Tributyl phosphate is a neurotoxic compound and an irritant. The toxic effects are characteristic of organic phosphates. It inhibits cholinesterase activity and causes paralysis. Inaddition,itcancausedepressionofthecentralnervoussystem,aswellasirritationofthe skin,eyes,andrespiratorypassage.Inhalation toxicity data in the literature are inconsistent.
The oral toxicity in rats was low; the LD50 value was reported as 1189 mg/kg (NIOSH 1986).
The pure liquid instilled into rabbits’ eyes caused severe irritation but no permanent damage. The irritation effect on the skin is mild.
Tributyl phosphate exhibited teratogenic effects in rats. There is no report on its carcinogenicity..

Пожароопасность

Special Hazards of Combustion Products: Toxic fumes of PO x

Промышленное использование

1. As an antifoaming agent.
2. As a plasticizer for cellulose esters, lacquers, plastics, and vinyl resins.
3. As a complexing agent in the extraction of heavy metals, especially for the extraction of metal ions from solutions of reactor products in nuclear fuel reprocessing.
4. As an aircraft hydraulic fluid.
5. As a heat exchange medium and dielectric.
6. As a pigment-grinding agent.

Профиль безопасности

Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion, inhalation, and subcutaneous routes. Experimental reproductive effects. A skin, eye, and mucous membrane irritant. Combustible when exposed to heat or flame. To fight fire, use CO2, dry chemical, fog, mist. When heated to decomposition it emits toxic fumes of POx.

Канцерогенность

TBP was not genotoxic in a variety of in vivo and in vitro assays.7 It has been suggested that the carcinogenic effects of TBP are species- and organ specific. The necrotic actions of TBP (or a metabolite) on rat urinary bladder epithelium may induce chronic repair processes that cause the normal epithelium to be transformed into its metaplastic and neoplastic forms.
TBP was not teratogenic when administered to rats and rabbits during gestation; fetotoxic effects (delayed ossification and reduced fetal body weights) occurred in rats at doses that caused severe maternal toxicity. There was no evidence of reproductive toxicity or reproductive organ pathology in twogeneration studies in rats fed TBP in the diet.

Экологическая судьба

Biological. Indigenous microbes in Mississippi River water degraded tributyl phosphate to carbon dioxide. After 4 wk, 90.8% of the theoretical carbon dioxide had evolved (Saeger et al., 1979).
Chemical/Physical. Complete hydrolysis yields 1-butanol and phosphoric acid via the intermediates dibutyl phosphate and monobutyl phosphate (Thomas and Macaskie, 1996).

Методы очистки

The main contaminants in commercial samples are organic pyrophosphates, monoand dibutyl phosphates and butanol. It is purified by washing successively with 0.2M HNO3 (three times), 0.2M NaOH (three times) and water (three times), then fractionally distilled under vacuum. [Yoshida J Inorg Nucl Chem 24 1257 1962.] It has also been purified via its uranyl nitrate addition compound, obtained by saturating the crude phosphate with uranyl nitrate. This compound is crystallised three times from n-hexane by cooling to -40o, and then decomposed by washing with Na2CO3 and water. Hexane is removed by steam distillation; the water is then evaporated under reduced pressure, and the residue is distilled under reduced pressure. [Siddall & Dukes J Am Chem Soc 81 790 1959.] Alternatively, wash it with water, then with 1% NaOH or 5% Na2CO3 for several hours, then finally with water. Dry it under reduced pressure and fractionate it carefully under vacuum. It is a stable colourless oil, sparingly soluble in H2O (1mL dissolves in 165mL of H2O), but freely miscible in organic solvents. [Kuivila & Masterton J Am Chem Soc 74 4953 1952, Cox & Westheimer J Am Chem Soc 80 5441 1958, 31P NMR: Van Wazer J Am Chem Soc 78 5715 1956, Fertig et al. J Chem Soc 1488 1957, Beilstein 1 IV 1531.]

Утилизация отходов

Tributyl phosphate is dissolved in a combustible solvent and is burned in a chemical incinerator equipped with an afterburner and scrubber.

ТРИБУТИЛФОСФАТ препаратная продукция и сырье

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