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P-фенилендиамин структурированное изображение

P-фенилендиамин

  • английское имяp-Phenylenediamine
  • CAS №106-50-3
  • CBNumberCB9852680
  • ФормулаC6H8N2
  • мольный вес108.14
  • EINECS203-404-7
  • номер MDLMFCD00007901
  • файл Mol106-50-3.mol
химическое свойство
Температура плавления 138-143 °C (lit.)
Температура кипения 267 °C (lit.)
Плотность накопления 600kg/m3
плотность 1.135 g/cm3 (20℃)
плотность пара 3.7 (vs air)
давление пара 1.08 mm Hg ( 100 °C)
показатель преломления 1.6339 (estimate)
Fp 156 °C
температура хранения Store below +30°C.
растворимость Soluble in alcohol, chloroform, ether and hot benzene.
Цветовой индекс 76060
форма Powder or Flakes
пка 4.17(at 25℃)
цвет White, gray, or purple to brown
Водородный показатель NonQ uorescence (3.1) to orange/yellow Q uorescence (4.4)
РН 9 (50g/l, H2O, 20℃)
Растворимость в воде 47 g/L (25 ºC)
Мерк 14,7285
БРН 742029
Пределы воздействия TLV-TWA 0.1 mg/m3 (ACGIH 1989); TWA skin 0.1 mg/m3 (MSHA and OSHA); IDLH 25 mg/m3 (NIOSH); carcinogenicity: Animal Inadequate Evidence (IARC). .
Стабильность Stable, but oxidizes when exposed to air. Incompatible with oxidizing agents. Store under inert atmosphere.
Основное приложение Nanoparticles, liquid crystal displays, chemical mechanical polishing, bottom antireflective coatings, electrochromic materials, inks, rubber, hair dyes, cosmetics, treatment of virus skin infection
ИнЧИКей CBCKQZAAMUWICA-UHFFFAOYSA-N
LogP -0.84 at 20℃
Непрямые добавки, используемые в веществах, контактирующих с пищевыми продуктами P-PHENYLENEDIAMINE
Справочник по базе данных CAS 106-50-3(CAS DataBase Reference)
Рейтинг продуктов питания EWG 5-7
FDA UNII U770QIT64J
Справочник по химии NIST 1,4-Benzenediamine(106-50-3)
МАИР 3 (Vol. 16, Sup 7) 1987
Система регистрации веществ EPA p-Phenylenediamine (106-50-3)
UNSPSC Code 12352204
NACRES NA.83
больше
Заявления об опасности и безопасности
Коды опасности T,N,T+,Xn
Заявления о рисках 23/24/25-36-43-50/53-63-36/37/38-45-40-48/22-67-52/53
Заявления о безопасности 28-36/37-45-60-61-28A-24/25-23-53-26
РИДАДР UN 1673 6.1/PG 3
OEB D
OEL TWA: 0.1 mg/m3 [skin]
WGK Германия 3
RTECS SS8050000
F 8-10-23
Температура самовоспламенения 567 °C
TSCA Yes
Класс опасности 6.1
Группа упаковки III
кода HS 29215119
Банк данных об опасных веществах 106-50-3(Hazardous Substances Data)
Токсичность LD50 in rats (mg/kg): 80 orally, 37 i.p. (Burnett)
ИДЛА 25 mg/m3
NFPA 704:
0
3 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms

  • сигнальный язык

    опасность

  • вредная бумага

    H319:При попадании в глаза вызывает выраженное раздражение.

    H301+H311+H331:Токсично при проглатывании, при контакте с кожей или при вдыхании.

    H317:При контакте с кожей может вызывать аллергическую реакцию.

    H410:Чрезвычайно токсично для водных организмов с долгосрочными последствиями.

    H370:Поражает органы (Глаза) в результате однократного воздействия.

  • оператор предупредительных мер

    P273:Избегать попадания в окружающую среду.

    P280:Использовать перчатки/ средства защиты глаз/ лица.

    P301+P310: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.

    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.

P-фенилендиамин MSDS

P-фенилендиамин химические свойства, назначение, производство

Описание

Paraphenylenediamine (PPD) is a colorless compound oxidized by hydrogen peroxide in the presence of ammonia. It is then polymerized by a coupling agent to produce a color.

Химические свойства

p-Phenylenediamines are white to slightly red crystalline solids. They have been described as gray “light brown” which may result from exposure to air.

Физические свойства

White, red, or brown crystals. May darken on exposure to air.

Использование

p-Phenylenediamine is used for dyeing hairand fur, in the manufacture of azo dyes, inaccelerating vulcanization of rubber, and inantioxidants.

Определение

ChEBI: A phenylenediamine in which the amino functions are at positions 1 and 4 of the benzene nucleus.

Общее описание

A white to purple crystalline solid (melting point 234 F) that turns purple to black in air. Flash point 309 F. Toxic by skin absorption, inhalation or ingestion. Used for production of aramid fiber, antioxidants, as a laboratory reagent, in photographic developing, and as a dye for hair and furs.

Реакции воздуха и воды

Oxidizes on exposure to air. The finely powdered base if suspended in air poses a significant dust explosion hazard. Soluble in water. Even as a solid will spot downwind areas purple/black (Roger Patrick, DuPont Engineer).

Профиль реактивности

p-Phenylenediamine is the stongest of the weak aromatic bases. p-Phenylenediamine neutralizes acids in weak exothermic reactions to form salts. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Reacts readily with oxidizing agents .

Пожароопасность

Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Контактные аллергены

PPD is a colorless compound oxidized by hydrogen peroxide in the presence of ammonia. It is then polymerized to a color by a coupling agent. Although a wellknown allergen in hair dyes, PPD can be found as a cause of contact dermatitis in chin rest stains or in milk testers. It is also a marker of group sensitivity to para amino compounds such as benzocaine, some azo dyes, and some previous antibacterial sulphonamides.

Профиль безопасности

Suspected carcinogen with experimental tumorigenic data. Poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Mildly toxic by skin contact. A human skin irritant. Mutation data reported. Implicated in aplastic anemia, Can cause fatal liver damage. The p-form is more toxic and a stronger irritant than the 0and misomers. Wen used as a hair dye it caused vertigo, anemia, gastritis, exfoliative dermatitis, and death. Has caused asthma and other respiratory symptoms in the fur-dyeing industry. Combustible when exposed to heat or flame; can react vigorously with oxidizing materials. To fight fire, use water, Con, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also other phenylenediamine entries and AMINES

Возможный контакт

p-Phenylenediamine has been used in dyestuff manufacture, in hair dyes; in photographic developers; in synthetic fibers; polyurethanes, and as a monomer and in the manufacture of improved tire cords. Also used as a gasoline additive and in making antioxidants.

Канцерогенность

A number of dermal carcinogenesis bioassays have been reported using p-PDA alone in an organic solvent or in combination with hydrogen peroxide. An 85-week study in which female Swiss mice were treated with 5% or 10% p-PDAin acetone, 0.02 mL/animal applied topically, showed no evidence of carcinogenicity.
p-PDA was not found to be carcinogenic when administered by diet to male and female F344 rats and B6C3F1 mice at the dietary doses of 625 or 1250 ppm; the high dose approximated the maximum tolerated dose. An IARC Working Group concluded that on the basis of lack of human data, and inadequate animal data, p-PDA was not classifiable as to its carcinogenicity to humans. A recent meta-analysis of 11 case-control studies and one cohort study of the relationship between p-PDA exposure through use of personal hair dye and bladder cancer did not indicate any causal association.

Экологическая судьба

Biological. In activated sludge, 3.8% mineralized to carbon dioxide after 5 d (Freitag et al., 1985). In activated sludge inoculum, following a 20-d adaptation period, 80.0% COD removal was achieved (Pitter, 1976).
Photolytic. A carbon dioxide yield of 53.7% was achieved when phenylenediamine (presumably an isomeric mixture) adsorbed on silica gel was irradiated with light (λ >290 nm) for 17 h (Freitag et al., 1985).
Chemical/Physical. p-Phenylenediamine will not hydrolyze because it does not contain a hydrolyzable functional group (Kollig, 1993).

Перевозки

UN1673 Phenylenediamines (o-, m-, p-), Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Методы очистки

Crystallise the diamine from EtOH or *benzene, and sublime it in vacuo; protect it from light. The acetate has m 304o. [Beilstein 13 IV 104.]

Несовместимости

Dust may form explosive mixture with air. A strong reducing agent. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, acid chlorides; acid anhydrides; chloroformates, and strong bases. Incompatible with organic anhydrides; isocyanates, aldehydes. Heat and light contribute to instability. Keep away from metals.

Утилизация отходов

Controlled incineration whereby oxides of nitrogen are removed from the effluent gas by scrubber, catalytic or thermal device.

P-фенилендиамин поставщик

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