Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство запасные части и сырье поставщик Обзор
Фуран-2 ,5-дикарбоновой кислоты структурированное изображение

Фуран-2 ,5-дикарбоновой кислоты

  • английское имя2,5-Furandicarboxylic acid
  • CAS №3238-40-2
  • CBNumberCB6264091
  • ФормулаC6H4O5
  • мольный вес156.09
  • EINECS221-800-8
  • номер MDLMFCD00016582
  • файл Mol3238-40-2.mol
химическое свойство
Температура плавления >300 °C
Температура кипения 240.29°C (rough estimate)
плотность 1.7400
показатель преломления 1.6400 (estimate)
температура хранения Keep in dark place,Sealed in dry,Room Temperature
растворимость DMSO (Slightly), Methanol (Slightly Sonicated)
форма Solid
пка 2.28±0.10(Predicted)
цвет White to Dark Brown
Растворимость в воде 1g/L(18 ºC)
Стабильность Light Sensitive, Very Hygroscopic
ИнЧИКей CHTHALBTIRVDBM-UHFFFAOYSA-N
LogP -1.43 at 20℃
Справочник по базе данных CAS 3238-40-2(CAS DataBase Reference)
FDA UNII 73C4JJ695C
Справочник по химии NIST Furan-2,5-dicarboxylic acid(3238-40-2)
Система регистрации веществ EPA 2,5-Furandicarboxylic acid (3238-40-2)
Заявления об опасности и безопасности
Коды опасности Xi
Заявления о рисках 36/37/38-36
Заявления о безопасности 26-36/37/39-36/37
WGK Германия 1
TSCA Yes
Класс опасности IRRITANT
кода HS 29321900
NFPA 704:
0
2 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H319:При попадании в глаза вызывает выраженное раздражение.

  • оператор предупредительных мер

    P280:Использовать перчатки/ средства защиты глаз/ лица.

    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.

    P337+P313:Если раздражение глаз не проходит обратиться за медицинской помощью.

Фуран-2 ,5-дикарбоновой кислоты химические свойства, назначение, производство

Описание

2,5-Furandicarboxylic acid (FDCA) is an organic chemical compound consisting of two carboxylic acid groups attached to a central furan ring. It was first reported as dehydromucic acid by Rudolph Fittig and Heinzelmann in 1876, who produced it via the action of concentrated hydrobromic acid upon mucic acid. It can be produced from certain carbohydrates and as such is a renewable resource, it was identified by the US Department of Energy as one of 12 priority chemicals for establishing the “green” chemistry industry of the future.Furan-2,5-dicarboxylic acid (FDCA) has been suggested as an important renewable building block because it can substitute for terephthalic acid (PTA) in the production of polyesters and other current polymers containing an aromatic moiety.
wikipedia

Химические свойства

2,5-Furandicarboxylic acid is a chemical intermediate with high sensitivity and good stability. It is soluble in water under alkaline conditions and is a white powder solid under acidic conditions, and is an important monomer for the preparation of corrosion-resistant plastics. It is irritating to eyes, respiratory tract and skin.

История

2,5-Furandicarboxylic acid, also known as dehydromucic acid, is a furan derivative. This organic compound was first obtained by Fittig and Heinzelmann in 1876. More than 125 years later, FDCA was identified by the US Department of Energy as one of 12 priority chemicals for establishing the "green" chemistry industry of the future. On a laboratory scale, it is often synthesized from 5- hydroxymethylfurfural (HMF), which in turn can be obtained from carbohydrate-containing sources such as glucose, fructose, sucrose, and starch. From fructose and glucose, HMF is obtained by acidic eliminating three moles of water.

Использование

Interest in renewable based polymers has led to 2,5-furandicarboxylic acid being proposed as a green, sustainable alternative to the widely used petroleum-based terephthalic acid in the synthesis of polyesters. 2,5-Furandicarboxylic acid is produced from oxidation of 5-hydroxymethylfurfural (HMF) which is obtained from the dehydration of bio-based sugars such as fructose.

Подготовка

2,5-Furandicarboxylic acid (FDCA) can be produced from biomass or its derived sugars or platform chemicals, and has demonstrated to be a very promising substitute for petroleum-derived polymer products.
Chapter 5 - Advances in the synthesis and application of 2,5-furandicarboxylic acid

Определение

ChEBI: A member of the class of furans carrying two carboxy substituents at positions 2 and 5.

прикладной

2,5-Furandicarboxylic acid (FDCA) is a renewable, greener substitute for terephthalate in the production of polyesters. It is widely used as a precursor for the synthesis of bio-based polyesters and various other polymers.
Applications of FDCA in the synthesis of several metal-organic frameworks (MOFs) have also been reported.

Фуран-2 ,5-дикарбоновой кислоты поставщик

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