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DL-5-Hydroxytryptophan
- английское имя5-Hydroxytryptophan
- CAS №56-69-9
- CBNumberCB0110022
- ФормулаC11H12N2O3
- мольный вес220.22
- EINECS200-284-8
- номер MDLMFCD00005651
- файл Mol56-69-9.mol
Температура плавления | 298-300°C |
Температура кипения | 361.16°C (rough estimate) |
плотность | 1.484 |
показатель преломления | 1.5200 (estimate) |
температура хранения | Keep in dark place,Sealed in dry,Room Temperature |
растворимость | DMSO (Slightly), Methanol (Slightly) |
форма | solid |
пка | 2.22±0.10(Predicted) |
цвет | Off-White to Pale Beige |
Растворимость в воде | Soluble in water (4 mg/ml at 25°C), methanol. |
Мерк | 14,4847 |
БРН | 88199 |
ИнЧИКей | LDCYZAJDBXYCGN-UHFFFAOYSA-N |
LogP | -0.292 (est) |
Справочник по базе данных CAS | 56-69-9(CAS DataBase Reference) |
Рейтинг продуктов питания EWG | 1 |
FDA UNII | 9181P3OI6N |
Система регистрации веществ EPA | Tryptophan, 5-hydroxy- (56-69-9) |
UNSPSC Code | 12352100 |
NACRES | NA.22 |
Заявления о безопасности | 26 | |||||||||
WGK Германия | 3 | |||||||||
RTECS | YN7100000 | |||||||||
Группа упаковки | III | |||||||||
Банк данных об опасных веществах | 56-69-9(Hazardous Substances Data) | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H302:Вредно при проглатывании.
H332:Вредно при вдыхании.
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оператор предупредительных мер
P261:Избегать вдыхания пыли/ дыма/ газа/ тумана/ паров/ аэрозолей.
P264:После работы тщательно вымыть кожу.
P270:При использовании продукции не курить, не пить, не принимать пищу.
P271:Использовать только на открытом воздухе или в хорошо вентилируемом помещении.
P301+P312:ПРИ ПРОГЛАТЫВАНИИ: Обратиться за медицинской помощью при плохом самочувствии.
P304+P340:ПРИ ВДЫХАНИИ: Свежий воздух, покой.
P312:Обратиться за медицинской помощью при плохом самочувствии.
P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.
DL-5-Hydroxytryptophan химические свойства, назначение, производство
Описание
5-Hydroxytryptophan (5-HTP) is an aromatic amino acid naturally produced by the body from the essential amino acid L-tryptophan (LT). Produced commercially by extraction from the seeds of the African plant, Griffonia simplicifolia, 5-HTP has been used clinically for over 30 years. The clinical efficacy of 5-HTP is due to its ability to increase production of serotonin in the brain.Химические свойства
Off-White to Pale Beige Solid, slightly salty in taste, soluble in methanol, ethanol, DMSO and other organic solvents, derived from African Ghana seeds.Использование
5-Hydroxytryptophan (5-HTP) is an intermediate in the natural synthesis of the essential amino acid, tryptophan, to serotonin. Clinical studies suggest that 5-HTP supports healthy serotonin levels. In the body, 5-HTP converts to serotonin with the enzymatic removal of a carboxyl group (COOH). Serotonin is an important neurotransmitter involved in the regulation of endocrine and brain activity responsible for emotion, appetite and sleep/wake cycles.Подготовка
The synthesis of 5-hydroxytryptophan (5-HTP) by the condensation of 5-benzyloxygramine with diethyl formaminomalonate, followed by saponification, decarboxylation, and hydrogenolysis was described in 1951 and 1954 and was an application of gramine synthesis, developed by Snyder and Smith ten years before. A few years later, another application of gramine synthesis was reported. In the same year, Frangatos and Chubb reported an application of the convenient tryptophan synthesis developed ten years before by eliminating the difficult and tedious preparation of 5-benzyloxyindole. The p-benzyloxyphenylhydrazone of γ,γ-dicarbethoxy-γ-acetamido-butyraldehyde (I) was prepared and cyclized, without isolation, to form ethyl β-(5-benzyloxyindol-3-)-αcarbethoxy-α-acetamidopropioilate (II). Saponification and partial decarboxylation of II, followed by hydrolysis of the acetamido group, gave 5-benzyloxytryptophan (III). 5-HTP was obtained by hydrogenolysis of III (Figure 1). However, this synthetic method suffers from the difficulty involved in the regioselective hydroxylation of tryptophan.
synthesis of 5-hydroxytryptophan (5-HTP)
Определение
ChEBI: 5-hydroxytryptophan is a tryptophan derivative that is tryptophan substituted by a hydroxy group at position 5. It has a role as a human metabolite and a neurotransmitter.прикладной
5-hydroxytryptophan is a dietary supplement made from the seeds of the African plant Griffonia simplicifolia.5-hydroxytryptophan has been used in alternative medicine as a possibly effective aid in treating depression or fibromyalgia.
Other uses not proven with research have included insomnia, alcohol withdrawal, headaches, premenstrual syndrome, binge-eating related to obesity, attention deficit disorder, and muscle spasms in the mouth.
5-hydroxytryptophan is often sold as an herbal supplement. There are no regulated manufacturing standards in place for many herbal compounds and some marketed supplements have been found to be contaminated with toxic metals or other drugs. Herbal/health supplements should be purchased from a reliable source to minimize the risk of contamination.
Биосинтез
5-Hydroxytryptophan, an intermediate molecule in the serotonin biosynthesis pathway, is formed by the addition of a hydroxyl (OH) group to the fifth carbon of the indole ring of tryptophan. It is used as an antiepileptic and antidepressant.DL-5-Hydroxytryptophan запасные части и сырье
DL-5-Hydroxytryptophan поставщик
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