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D(-)-винная кислота структурированное изображение

D(-)-винная кислота

  • английское имяD-(-)-Tartaric Acid
  • CAS №147-71-7
  • CBNumberCB3693922
  • ФормулаC4H6O6
  • мольный вес150.09
  • EINECS205-695-6
  • номер MDLMFCD00004238
  • файл Mol147-71-7.mol
химическое свойство
Температура плавления 172-174 °C(lit.)
альфа -12.1 º (c=20, H2O)
Температура кипения 191.59°C (rough estimate)
плотность 1,8 g/cm3
показатель преломления -12.5 ° (C=5, H2O)
Fp 210 °C
температура хранения Store below +30°C.
растворимость water: soluble100mg/mL, clear, colorless
форма Crystals or Crystalline Powder
пка 3.0, 4.4(at 25℃)
цвет White
Запах odorless
оптическая активность [α]20/D 13.5±0.5°, c = 10% in H2O
Растворимость в воде 1394 g/L (20 ºC)
Чувствительный Light Sensitive
Мерк 14,9068
БРН 1725145
Диэлектрическая постоянная 35.9(-10℃)
Стабильность Stable. Incompatible with oxidizing agents, bases, reducing agents. Combustible.
ИнЧИКей FEWJPZIEWOKRBE-LWMBPPNESA-N
LogP -1.081 (est)
FDA 21 CFR 310.545
Справочник по базе данных CAS 147-71-7(CAS DataBase Reference)
Рейтинг продуктов питания EWG 1
FDA UNII RRX6A4PL3C
Справочник по химии NIST D-Tartaric acid(147-71-7)
Система регистрации веществ EPA Butanedioic acid, 2,3-dihydroxy-, (2S,3S)- (147-71-7)
больше
Заявления об опасности и безопасности
Коды опасности Xi
Заявления о рисках 36/37/38
Заявления о безопасности 26-36/37-37/39-36
WGK Германия 3
RTECS WW7875000
Температура самовоспламенения 425 °C
Примечание об опасности Light Sensitive
TSCA Yes
кода HS 29181200
NFPA 704:
1
2 0

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    опасность

  • вредная бумага

    H318:При попадании в глаза вызывает необратимые последствия.

  • оператор предупредительных мер

    P280:Использовать перчатки/ средства защиты глаз/ лица.

    P305+P351+P338+P310: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. Немедленно обратиться за медицинской помощью.

D(-)-винная кислота MSDS

D(-)-винная кислота химические свойства, назначение, производство

Описание

D-Tartaric acid, also known as (S, S)-tartrate or D-threaric acid, belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group. D-Tartaric acid has been detected but not quantified in loquats (Eriobotrya japonica). This could make D-tartaric acid a potential biomarker for consuming these foods. D-Tartaric acid is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve as defense or signalling molecules. In some cases, they are molecules that arise from the incomplete metabolism of other secondary metabolites.

Химические свойства

D-Tartaric acid is a white crystalline dicarboxylic acid found in many plants, particularly tamarinds and grapes. It is an acidulant that occurs naturally in grapes. It is hygroscopic and rapidly soluble, with a solubility of 150 g in 100 ml of distilled water at 25°c. It has a slightly tarter taste than citric acid, with a tartness equivalent of 0.8–0.9. It augments the flavor of fruits in which it is a natural constituent. It is used in grapeand limeflavored beverages and grape-flavored jellies. It is used as an acidulant in baking powder and as a synergist with antioxidants to prevent rancidity.

Использование

D-(-)-Tartaric acid is commonly used as a resolving agent in organic synthesis. It is the synthetic enantiomer of L-(+)-Tartaric acid and is utilized in the production of synthetic analgesics. Tartaric acid is the second largest alpha hydroxy acid (AHA) in terms of size, with glycolic acid being the smallest and citric acid being the largest. It serves as a precursor for the synthesis of ester derivatives such as D-tartaric acid diethyl ester, D-tartaric acid dimethyl ester, and D-tartaric acid diiso-propyl ester. Moreover, it is employed in the creation of chiral aziridine derivative, which is a common intermediate for manufacturing hydroxyethylamine class HIV protease inhibitors like saquinavir, amprenavir, and nelfinavir. In the food industry, it is extensively used as a beer foaming agent, for regulating food acidity, and as a flavoring agent. However, due to its challenging workability and potential skin irritation, it is not frequently utilized in cosmetic or anti-aging preparations.

Определение

ChEBI: D-tartaric acid is the D-enantiomer of tartaric acid. It has a role as an Escherichia coli metabolite. It is a conjugate acid of a D-tartrate(1-). It is an enantiomer of a L-tartaric acid.

Общее описание

D-(-)-Tartaric acid is a polycrystalline solid, widely used as food additive. It has been reported to exhibit piezoelectric effect.

Методы очистки

Crystallise the acid from distilled H2O or *benzene/diethyl ether containing 5% of pet ether (b 60-80o) (1:1). Soxhlet extraction with diethyl ether has been used to remove an impurity absorbing at 265nm. It has also been crystallised from absolute EtOH/hexane and dried in a vacuum for 18hours [Kornblum & Wade J Org Chem 52 5301 1987]. [Beilstein 3 IV 1229.]

D(-)-винная кислота поставщик

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