트립타민
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트립타민 속성
- 녹는점
- 113-116 °C (lit.)
- 끓는 점
- 137 °C/0.15 mmHg (lit.)
- 밀도
- 0.9787 (rough estimate)
- 굴절률
- 1.6210 (estimate)
- 인화점
- 185 °C
- 저장 조건
- 2-8°C
- 용해도
- 물: 20°C에서 용해성 1g/L
- 산도 계수 (pKa)
- 10.2(at 25℃)
- 물리적 상태
- 수정 같은
- 색상
- 하얀색
- 수소이온지수(pH)
- 11.07 (10g/l, H2O, 24.7℃)
- 수용성
- 무시할 만한
- 감도
- Air Sensitive
- Merck
- 14,9796
- BRN
- 125513
- CAS 데이터베이스
- 61-54-1(CAS DataBase Reference)
안전
- 위험 및 안전 성명
- 위험 및 사전주의 사항 (GHS)
| 위험품 표기 | Xi | ||
|---|---|---|---|
| 위험 카페고리 넘버 | 20/21/22-36/37/38-41-37/38-22 | ||
| 안전지침서 | 24/25-36/37/39-36-26 | ||
| WGK 독일 | 3 | ||
| RTECS 번호 | NL4020000 | ||
| F 고인화성물질 | 8-23 | ||
| 위험 등급 | IRRITANT | ||
| HS 번호 | 28259080 | ||
| HS 번호 | 29339990 | ||
| 기존화학 물질 | KE-01371 |
트립타민 C화학적 특성, 용도, 생산
개요
Tryptamine is an indole alkaloid and intermediate in the biosynthesis of serotonin and the phytohormone melatonin in plants. It increases the levels of the terpenoid indole alkaloids ajmalicine, strictosidine, and catharanthine in cultures of C. roseus. Tryptamine is also a product of tryptophan metabolism in mammals. Tryptamine derivatives have been synthetically produced as hallucinogenic drugs of abuse that act on the serotonergic system.화학적 성질
Tryptamine is a biogenic imine derived from the decarboxylation of tryptophan. It is a white to orange crystalline Powder, melting point 118°C (decomposition at 145-146°C). Soluble in ethanol and acetone, almost insoluble in ether, benzene, chloroform and water.용도
Tryptamine is a monoamine alkaloid found in plants. Tryptamine is commonly used in the preparation of biologically active compounds such as neurotransmitters and psychedelics.정의
ChEBI: Tryptamine is an aminoalkylindole consisting of indole having a 2-aminoethyl group at the 3-position. It has a role as a human metabolite, a plant metabolite and a mouse metabolite. It is an aminoalkylindole, an indole alkaloid, an aralkylamino compound and a member of tryptamines. It is a conjugate base of a tryptaminium.제조 방법
Tryptamine, a monoamine alkaloid containing an indole ring structure is derived by the decarboxylation of amino acid tryptophan.
The synthesis of tryptamines is typically conducted following a classic route starting with a Mannich reaction of an indole heterocycle, followed by quaternization of the amine, nucleophilic substitution with highly toxic cyanide and final reduction.
일반 설명
Tryptamines which are usually found in plants, fungi, animals, etc. are categorized under the monoamine alkaloids class of compounds.Purification Methods
Crystallise tryptamine from *benzene, Et2O (m 114o) or pet ether (m 118o). It has UV: 222n 276, 282 and 291nm (EtOH) and max 226, 275, 281 and 290nm (HCl). [Beilstein 22 II 346, 22 III/IV 4319, 22/10 V 45.]트립타민 준비 용품 및 원자재
원자재
준비 용품
Vinpocetine
1,2,3,4-TETRAHYDRO-9H-PYRIDO[3,4-B]INDOLE
N,N-Dimethyltryptamine
빈카민
N-(p-Coumaroyl) Serotonin
1-TRIFLUOROMETHYL-2,3,4,9-TETRAHYDRO-1H-B-CARBOLINE
N-METHYL-N-ISOPROPYLTRYPTAMINE(MIPT)
TETRAHYDROALSTONINE
3-Ethylindole
2-cyano-N-[2-(1H-indol-3-yl)ethyl]acetamide
N-(2-INDOL-3-YLETHYL)(4-METHYLPHENYL)FORMAMIDE
N-(2-INDOL-3-YLETHYL)-3-PHENYLPROP-2-ENAMIDE
트립타민 공급 업체
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