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Аденин

Аденин структура
73-24-5
CAS №
73-24-5
Химическое название:
Аденин
английское имя:
Adenine
Синонимы:
9H-Purin-6-amine;Adenin;6-AMINOPURINE;Vitamin B4;7H-PURIN-6-AMINE;Ade;ANE;Purin-6-amine;1H-PURIN-6-AMINE;6-Amino-9H-purine
CBNumber:
CB1323708
Формула:
C5H5N5
молекулярный вес:
135.13
MOL File:
73-24-5.mol

Аденин атрибут

Температура плавления: >360 °C (lit.)
Температура кипения: 238.81°C (rough estimate)
плотность: 1.3795 (rough estimate)
показатель преломления: 1.7000 (estimate)
Fp: 220°C
температура хранения: 2-8°C
растворимость: 0,5 М HCl: растворим 20 мг/мл, класс III, от бесцветного до бледно-желтого или желтовато-коричневого
форма: Жидкость или твердое тело
пка: 4.12(at 25℃)
цвет: Прозрачный от бесцветного до светло-желтого
Запах: Без запаха
Водородный показатель: 7
Растворимость в воде: 0,5 г/л (20°С)
Сублимация: 220 ºC
Мерк: 14,152
БРН: 5777
Стабильность:: Стабильный. Чувствителен к влаге. Несовместим с сильными окислителями.
ИнЧИКей: GFFGJBXGBJISGV-UHFFFAOYSA-N
LogP: -0.090
Справочник по базе данных CAS: 73-24-5(CAS DataBase Reference)
Рейтинг продуктов питания EWG: 1
Словарь онкологических терминов NCI: ADE; adenine
FDA UNII: JAC85A2161
Справочник по химии NIST: Adenine(73-24-5)
Система регистрации веществ EPA: Adenine (73-24-5)
безопасность
  • Заявления о рисках и безопасности
  • код информации об опасности(GHS)
Коды опасности Xn,Xi
Заявления о рисках 22-20/21/22
Заявления о безопасности 26-36
РИДАДР UN 2811 6.1/PG 3
WGK Германия 3
RTECS AU6125000
F 8-10-23
TSCA Yes
Класс опасности 6.1
Группа упаковки III
кода HS 29335990
Токсичность LD50 orally in rats: 745 mg/kg (Philips)
символ(GHS) GHS hazard pictograms
сигнальное слово Danger
Заявление об опасности
пароль Заявление об опасности Класс опасности категория сигнальное слово пиктограмма предупреждение
H301 Токсично при проглатывании. Острая токсичность, пероральная Категория 3 Опасность GHS hazard pictograms P264, P270, P301+P310, P321, P330,P405, P501
Внимание
P301+P310+P330 ПРИ ПРОГЛАТЫВАНИИ: Немедленно обратиться за медицинской помощью. Прополоскать рот.

Аденин MSDS


6-Aminopurine

Аденин химические свойства, назначение, производство

Описание

adenine is one of the purine nitrogenous bases that composes DNA and RNA; composed of two carbon–nitrogen rings. Adenine bonds with thymine in DNA and with uracil in RNA (see base pairing rule); it is also a major component of other molecules such as adenosine triphosphate.

Химические свойства

Adenine is a prominent member of the family of naturally occurring purines. Adenine occurs not only in ribonucleic acids (RNA), and deoxyribonucleic acids (DNA), but in nucleosides, such as adenosine, and nucleotides, such as adenylic acid, which may be linked with enzymatic functions quite apart from nucleic acids. Adenine, in the form of its ribonucleotide, is produced in mammals and fowls endogenously from smaller molecules and no nutritional essentiality is ascribed to it. In the nucleosides, nucleotides, and nucleic acids, the attachment or the sugar moiety is at position 9.
The purines and pyrimidines absorb ultraviolet light readily, with absorption peaks at characteristic frequencies. This has aided in their identification and quantitative determination.

Физические свойства

Adenine is a white to almost white crystalline powder that is an important biological compound found in deoxyribonucleic acid (DNA), ribonucleic acid (RNA), and adenosine triphosphate (ATP). It was once commonly referred to as vitamin B4 but is no longer considered a vitamin. Adenine is derived from purine. Purine is a heterocyclic compound.

История

Adenine is one of the two purines found in DNA and RNA. The other is guanine. Adenine and guanine are called bases in reference to DNA and RNA. A nucleic acid base attached to ribose forms a ribonucleoside. Adenine combined with ribose produces the nucleoside adenosine.

Использование

Adenine is used as an active component of boron-deficient media to grow yeast in order to assess whether yeast growth is stimulated by boron. It is useful as a local antiseptic and vitamin B4. Further, it is used in the microbial determination of niacin. It is also employed as a food supplement for adult rats to investigate the effects of dietary adenine overload. In addition to this, it is used in the production of nucleotides of the nucleic acids.

Определение

ChEBI: Adenine is the parent compound of the 6-aminopurines, composed of a purine having an amino group at C-6. It has a role as a human metabolite, a Daphnia magna metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a purine nucleobase and a member of 6-aminopurines. It derives from a hydride of a 9H-purine.

прикладной

Widespread throughout animal and plant tissues combined with niacinamide, d-ribose, and phosphoric acids; a constituent of nucleic acids and coenzymes, such as codehydrase I and II, adenylic acid, coa laninedehydrase. It is used in microbial determination of niacin; in research on heredity, virus diseases, and cancer.

Общее описание

Adenine is a purine nucleobase. It is part of DNA, and RNA. Adenine is also a component of cofactors (NAD, FAD) and signaling molecules (cAMP). It is a nitrogenous base found in DNA and RNA. It is also a constituent of certain coenzymes and when combined with the sugar ribose it forms the nucleoside adenosine found in AMP, ADP, and ATP. Adenine has a purine ring structure. It is one of the major component bases ofnucleotides and the nucleic acidsDNA and RNA.

Профиль безопасности

Poison by intraperitoneal route. Moderately toxic by ingestion. An experimental teratogen. Experimental reproductive effects. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx,.

Методы очистки

Crystallise adenine from distilled water. [Beilstein 26 III/IV 3561.]

Аденин препаратная продукция и сырье

сырьё

препарат


Аденин поставщик

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