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Бензилбензоат

Бензилбензоат структура
120-51-4
CAS №
120-51-4
Химическое название:
Бензилбензоат
английское имя:
Benzyl benzoate
Синонимы:
benzyl benzonate;Benzyl ester;ASCABIOL;Benzylbenzoat;Benzyl Benoate;BENZOATO DE BENCILO;Nat.Benzyl benzoate;BENZOIC ACID BENZYL ESTER;BENZOIC ACID PHENYLMETHYL ESTER;Benzoic acid benzyl ester≥ 99% (GC)
CBNumber:
CB9152283
Формула:
C14H12O2
молекулярный вес:
212.24
MOL File:
120-51-4.mol

Бензилбензоат атрибут

Температура плавления: 17-20 °C (lit.)
Температура кипения: 323-324 °C (lit.)
плотность: 1.118 g/mL at 20 °C (lit.)
давление пара: 1 mm Hg ( 125 °C)
показатель преломления: n20/D 1.568(lit.)
FEMA: 2138 | BENZYL BENZOATE
Fp: 298 °F
температура хранения: 2-8°C
растворимость: Смешивается с этанолом, спиртом, хлороформом, эфиром, маслами.
форма: жидкость
цвет: Прозрачный бесцветный
Запах: at 100.00 %. faint sweet balsam oily herbal
Odor Type: balsamic
Растворимость в воде: практически нерастворимый
Мерк: 14,1127
Номер JECFA: 24
БРН: 2049280
Диэлектрическая постоянная: 4.8(20℃)
Стабильность:: Стабильный. Вещества, которых следует избегать, включают сильные окислители. Горючий.
ИнЧИКей: SESFRYSPDFLNCH-UHFFFAOYSA-N
LogP: 4 at 20℃
Справочник по базе данных CAS: 120-51-4(CAS DataBase Reference)
Вещества, добавляемые в пищу (ранее EAFUS): BENZYL BENZOATE
FDA 21 CFR: 172.515; 175.105; 310.545
Рейтинг продуктов питания EWG: 3-6
FDA UNII: N863NB338G
Справочник по химии NIST: Benzyl Benzoate(120-51-4)
Код УВД: P03AX01
Пестициды: Закон о свободе информации (FOIA): Benzyl benzoate
Система регистрации веществ EPA: Benzyl benzoate (120-51-4)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xn,N
Заявления о рисках 22-51/53
Заявления о безопасности 25-61-46
РИДАДР UN 3082 9 / PGIII
WGK Германия 2
RTECS DG4200000
Температура самовоспламенения 896 °F
TSCA Yes
Класс опасности 9
кода HS 29163100
Банк данных об опасных веществах 120-51-4(Hazardous Substances Data)
Токсичность LD50 in rats, mice, rabbits, guinea pigs (g/kg): 1.7, 1.4, 1.8, 1.0 orally (Draize)
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
H411 Токсично для водных организмов с долгосрочными последствиями. Опасность для водной среды, долгосрочная опасность Категория 2
Внимание
P264 После работы тщательно вымыть кожу.
P270 При использовании продукции не курить, не пить, не принимать пищу.
P273 Избегать попадания в окружающую среду.
P301+P312 ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P391 Ликвидировать просыпания/проливы/утечки.
P501 Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.

Бензилбензоат MSDS


Benzyl benzoate

Бензилбензоат химические свойства, назначение, производство

Описание

Benzyl benzoate is the ester of benzyl alcohol and benzoic acid, with the formula C6H5CH2O2CC6H5. This easily prepared compound with a mild balsamic odor has a variety of uses.Benzyl benzoate (BB) is one of the oldest drugs used for the treatment of scabies and is recommended as the “first-line intervention” for the cost-effective treatment of the disease.

Химические свойства

Benzyl Benzoate is the main component of Peru balsam oil. It occurs in fairly large amounts in a number of blossom concretes and absolutes (e.g., tuberose and hyacinth). It forms either a viscous liquid or solid flakes (mp 21–22°C) and has a weak, sweet, balsamic odor.
Benzyl Benzoate
Benzyl Benzoate is prepared either by transesterification of technical methyl benzoate with benzyl alcohol or from benzyl chloride and sodium benzoate. A third process starts with benzaldehyde, which is converted in high yield into benzyl benzoate in the presence of sodium or aluminum benzylate (Tishchenko reaction). Benzyl benzoate is used in perfumery as a fixative and as a modifier in heavy blossom fragrances.

Вхождение

Contained in Peru balsam and in the concrete and absolute of tuberose flowers, hyacinth, Narcissus jonquilla L., and Dianthus caryophillus L.; also in the oil of ylang-ylang and in Tolu balsam. Reported found in American cranberry, cinnamon bark, cassia leaf, corn oil and hog plum (Spondias mombins L.).

Использование

benzyl benzoate is an anti-microbial. It can also act as a solvent, helping dissolve other substances in the product, and as a perfuming ingredient. It is the ester of benzyl alcohol and benzoic acid.

Определение

ChEBI: Benzyl benzoate is a benzoate ester obtained by the formal condensation of benzoic acid with benzyl alcohol. It has been isolated from the plant species of the genus Polyalthia. It has a role as a scabicide, an acaricide and a plant metabolite. It is a benzyl ester and a benzoate ester. It is functionally related to a benzoic acid.

Определение

Benzyl benzoate is produced from benzyl alcohol and sodium benzoate in the presence of triethylamine or by transesterification of methyl benzoate with benzyl alcohol in the presence of an alkali benzyl oxide. In another manufacturing process benzaldehyde is condensed to form benzyl benzoate in the presence of sodium (Claisen-Tishchenko condensation). The presence of a small amount of an aliphatic ether improves this reaction. Benzyl benzoate is a byproduct in the manufacture of benzoic acid by the oxidation of toluene; it is present in the benzoic acid distillation residue.

Подготовка

By the dry esterification of sodium benzoate and benzoyl chloride in the presence of triethylamine or by reaction of sodium benzylate on benzaldehyde.

Показания

Benzyl benzoate: 20% to 25%. This agent is relatively nontoxic and is widely used in developing countries to treat scabies and pediculosis capitis and pubis. Only a veterinary preparation is available in the United States. Benzyl benzoate is synthetically derived from the esterification of benzoic acid with benzyl alcohol. Its mechanism of action is unknown. It is toxic to Sarcoptes scabei and may be toxic to Pediculosis capitis and Phthirus pubis. No resistance has been demonstrated to date.
Benzyl benzoate can be used in a 5% emulsion to repel many arthropods and can be used as a lotion to treat sarcoptic mange and canine pediculosis.

Методы производства

BENZYL BENZOATE is produced by the Cannizzaro reaction from benzaldehyde, by esterifying benzyl alcohol with benzoic acid, or by treating sodium benzoate with benzyl chloride. It is purified by distillation and crystallization. Benzyl benzoate is used as a fixative and solvent for musk in perfumes and flavors, as a plasticizer, miticide, and in some external medications. The compound has been found effective in the treatment of scabies and pediculosis capitis (head lice, Pediculus humanus var. capitis).

Общее описание

Benzyl benzoate is an aromatic ester that is used as a food flavoring agent. It has been identified as one of the main volatile aroma component of cranberry, mango and Egyptian Jasminum sambac flowers.

Опасность

Irritant to eyes, skin.

Фармацевтические приложения

Benzyl benzoate is used as a solubilizing agent and nonaqueous solvent in intramuscular injections at concentrations of 0.01–46.0% v/v, and as a solvent and plasticizer for cellulose and nitrocellulose. It is also used in the preparation of spray-dried powders using nanocapsules.
However, the most widespread pharmaceutical use of benzyl benzoate is as a topical therapeutic agent in the treatment of scabies. Benzyl benzoate is also used therapeutically as a parasiticide in veterinary medicine.
Other applications of benzyl benzoate include its use as a pediculicide, and as a solvent and fixative for flavors and perfumes in cosmetics and food products.

Контактные аллергены

Benzyl benzoate is the ester of benzyl alcohol and benzoic acid. It is contained in Myroxylon pereirae and Tolu balsam. It is used in acaricide preparations against Sarcoptes scabiei or as a pediculicide. Direct contact may cause skin irritation, but rarely allergic contact dermatitis. As a fragrance allergen, benzyl benzoate has to be mentioned by name in EU cosmetics.

Клиническое использование

Benzyl benzoate is a naturally occurring ester obtained fromPeru balsam and other resins. It is also prepared syntheticallyfrom benzyl alcohol and benzoyl chloride. The ester isa clear colorless liquid with a faint aromatic odor. It is insolublein water but soluble in organic solvents.
Benzyl benzoate is an effective scabicide when appliedtopically. Immediate relief from itching probably resultsfrom a local anesthetic effect; however, a complete cureis frequently achieved with a single application of a 25%emulsion of benzyl benzoate in oleic acid, stabilized withtriethanolamine. This preparation has the additionaladvantage of being essentially odorless, nonstaining, andnonirritating to the skin. It is applied topically as a lotionover the entire dampened body, except the face.

Безопасность

Benzyl benzoate is metabolized by rapid hydrolysis to benzoic acid and benzyl alcohol. Benzyl alcohol is then further metabolized to hippuric acid, which is excreted in the urine.
Benzyl benzoate is widely used as a 25% v/v topical application in the treatment of scabies and as an excipient in intramuscular injections and oral products. Adverse reactions to benzyl benzoate include skin irritation and hypersensitivity reactions. Oral ingestion may cause harmful stimulation of the CNS and convulsions. Benzyl benzoate should be avoided by perople with perfume allergy.
LD50 (cat, oral): 2.24 g/kg
LD50 (dog, oral): 22.44 g/kg
LD50 (guinea pig, oral): 1.0 g/kg
LD50 (mouse, oral): 1.4 g/kg
LD50 (rabbit, oral): 1.68 g/kg
LD50 (rabbit, skin): 4.0 g/kg
LD50 (rat, oral): 0.5 g/kg
LD50 (rat, skin): 4.0 g/kg

Экологическая судьба

Benzyl benzoate acts as a local irritant. At high levels of exposure, free benzoic acid may sequester significant amounts of acetyl coenzyme A (CoA), which could disrupt cholinergic signaling. Recent findings suggest that benzyl benzoate may have estrogenic properties.

Метаболизм

Benzyl benzoate, a relatively non-toxic liquid widely used for the treatment of scabies, is converted into benzoic acid in vivo (Williams, 1959).

хранилище

Benzyl benzoate is stable when stored in tight, well-filled, lightresistant containers. Exposure to excessive heat (above 408℃) should be avoided.

Несовместимости

Benzyl benzoate is incompatible with alkalis and oxidizing agents.

Регуляторный статус

Included in the FDA Inactive Ingredients Database (IM injections and oral capsules). Included, as an active ingredient, in nonparenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

Бензилбензоат препаратная продукция и сырье

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