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L-изолейцин структурированное изображение

L-изолейцин

  • английское имяL-Isoleucine
  • CAS №73-32-5
  • CBNumberCB2678131
  • ФормулаC6H13NO2
  • мольный вес131.17
  • EINECS200-798-2
  • номер MDLMFCD00064222
  • файл Mol73-32-5.mol
химическое свойство
Температура плавления 288 °C (dec.) (lit.)
альфа 41 º (c=4, 6N HCl)
Температура кипения 225.8±23.0 °C(Predicted)
плотность 1.2930 (estimate)
FEMA 4675 | L-ISOLEUCINE
показатель преломления 40.5 ° (C=4, 6mol/L HCl)
Fp 168-170°C
температура хранения Store below +30°C.
растворимость 1 M HCl: 50 mg/mL
форма powder
пка 2.32, 9.76(at 25℃)
цвет White to Off-white
РН 5.5-6.5 (40g/l, H2O, 20℃)
Запах odorless
оптическая активность [α]20/D +41.0±1°, c = 5% in 6 M HCl
Растворимость в воде 41.2 g/L (50 ºC)
λмакс λ: 260 nm Amax: 0.07
λ: 280 nm Amax: 0.05
Номер JECFA 2118
Мерк 14,5179
Сублимация 168-170 ºC
БРН 1721792
ИнЧИКей AGPKZVBTJJNPAG-WHFBIAKZSA-N
LogP 0.80
Вещества, добавляемые в пищу (ранее EAFUS) L-ISOLEUCINE
FDA 21 CFR 172.320
Справочник по базе данных CAS 73-32-5(CAS DataBase Reference)
FDA UNII 04Y7590D77
Справочник по химии NIST Isoleucine(73-32-5)
Система регистрации веществ EPA L-Isoleucine (73-32-5)
больше
Заявления об опасности и безопасности
Коды опасности Xn
Заявления о рисках 40
Заявления о безопасности 24/25-36-22
WGK Германия 3
RTECS NR4705000
TSCA Yes
кода HS 29224995
Банк данных об опасных веществах 73-32-5(Hazardous Substances Data)
Токсичность LD50 intraperitoneal in rat: 6822mg/kg
NFPA 704:
1
1 1

рисовальное письмо(GHS)

  • рисовальное письмо(GHS)

    GHS hazard pictograms

  • сигнальный язык

    предупреждение

  • вредная бумага

    H315:При попадании на кожу вызывает раздражение.

    H319:При попадании в глаза вызывает выраженное раздражение.

    H335:Может вызывать раздражение верхних дыхательных путей.

  • оператор предупредительных мер

    P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.

    P271:Использовать только на открытом воздухе или в хорошо вентилируемом помещении.

    P280:Использовать перчатки/ средства защиты глаз/ лица.

L-изолейцин MSDS

L-изолейцин химические свойства, назначение, производство

Описание

Crystalline leaflets or a white, crystalline powder having a bitter taste. It is soluble in 25 parts of water, slightly soluble in hot alcohol, and soluble in diluted mineral acids and in alkaline solutions. It sublimes at between 168°C and 170°C, and melts with decomposition at about 284°C. The pH of a 1 in 100 solution is between 5.5 and 7.0.
Absolute: The absolute is prepared by alcoholic extraction of the concrete in approximately 55 to 60% yields. The absolute consists of a semisolid, olive-green mass with a characteristic ambergris odor.
Resinoid and Resin Absolute: The resinoid consists of the hydro carbon extract of the crude resin. The resin absolute consists of the alcoholic extract of the crude labdanum resin. Since this prod uct is a semisolid, nonpourable mass, a high-boiling, odorless solvent may be added prior to evaporation of the alcohol to prepare a pourable liquid.

Химические свойства

White crystalline powder

Использование

L-Isoleucine, also known as Isoleucine, is an amino acid that is an isomer of leucine. It is important in hemoglobin synthesis and regulation of blood sugar and energy levels.
L-Isoleucine is one of the essential amino acids that cannot be made by the body and is known for its ability to help endurance and assist in the repair and rebuilding of muscle. This amino acid is important to body builders as it helps boost energy and helps the body recover from training.
L-Isoleucine is also classified as a branched-chain amino acid (BCAA). There are three branched-chain amino acids in the body, with the others being L-Valine, and L-Leucine, and all of them help promote muscle recovery after exercise. Isoleucine is actually broken down for energy within the muscle tissue.

Методы производства

An advantageous fermentation method for production of L-isoleucine is the use of chemically synthesized substrates that only require a few steps to be converted to L-isoleucine. Among these the natural precursors 2-ketobutyrate or D,L-2-hydroxybutyrate have been used for the production with Corynebacterium glutamicum. A leucine requiring mutant of Corynebacterium glutamicum, with increased D-lactate utilization and consuming D,L-2-hydroxybutyrate, accumulates 13.4 g/L L-isoleucine. However, exploitation of this process is hampered by formation of byproducts. Sugar based L-isoleucine processes have been developed with strains of Corynebacterium glutamicum Serratia marcescens, and Escherichia coli. The mutant Escherichia coli H- 8285, being resistant to thiaisoleucine, arginine hydroxamate, and D,L-ethionine accumulates 26 g/L L-isoleucine in 45 h in a fed-batch process. Introduction of resistance to 6-dimethylaminopurine in strain H-8285 resulted in a mutant Escherichia coli H-8461 that increased L-isoleucine accumulation to 30.2 g/L. The biosynthesis of L-isoleucine has been investigated in detail on the level of involved genes, thus recombinant strains are being constructed with high productivity and selectivity. An appropriate balance of homoserine dehydrogenase and threonine dehydratase activities in the construct Corynebacterium glutamicum DR17/pECM3::ilvA (V323A) with feedback-resistant aspartate kinase create a specific productivity of 0.052 g L-isoleucine per gram dry biomass per hour. The recombinant strain Escherichia coli AJ13100 produces L-isoleucine from glucose with high selectivity in 30% yield.

Определение

ChEBI: The L-enantiomer of isoleucine.

Побочные эффекты

L-Isoleucine is generally considered a safe ingredient. The side effects may: Intake of Isoleucine can lead to nausea. Large doses can result in a stomach upset and indigestion.

Методы очистки

Crystallise L-isoleucine from H2O by addition of 4 volumes of EtOH or from aqueous MeOH. It sublimes at 170-181o/0.3mm with 99.7% recovery, unracemised [Gross & Gradsky J Am Chem Soc 77 1678 1955]. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 1 p 183-191, Vol 3 pp 2043-2073 1961, Huffman & Ingersoll J Am Chem Soc 73 3366 1951, Beilstein 4 IV 2775.]

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