基本情報
- 標準SMILES
OCCc1c[nH]c2ccccc12- InChIKey
MBBOMCVGYCRMEA-UHFFFAOYSA-N- 分子式
- C10H11NO
- 平均分子量
- 161.2 g/mol
- 単同位体質量
- 161.08406397
概要
Tryptophol is an indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. It has a role as an auxin, a Saccharomyces cerevisiae metabolite and a plant metabolite.
名称と識別子
- 優先名称
- Tryptophol
- IUPAC
- 2-(1H-indol-3-yl)ethanol
- 現地名
- 3-インドールエタノール
- 英語名
- Tryptophol
- 分子式
- C10H11NO
- 分子量
- 161.2
名称と別名
名称をさらに表示
データベース識別子
- CAS
526-55-6- PubChem CID
- 10685
- DTXSID
DTXSID2060173- ChEMBL
CHEMBL226545- ChEBI
CHEBI:17890- UNII
- 5809LZ7G1U
- EC Number
- 208-393-2
- Nikkaji
- J6.661C
物性
構造計算による物性
- XLogP
- 1.8
- 極性表面積
- 36 Ų
- 水素結合供与体数
- 2
- 水素結合受容体数
- 1
- 回転可能結合数
- 2
- 重原子数
- 12
- 形式電荷
- 0
- 複雑度
- 149
実験および物理化学的性質
Physical Description
Solid; [Merck Index] Brown or yellow solid; [Alfa Aesar MSDS]
Solid
Collision Cross Section
133.6 Ų [M+H]+ [CCS Type: DT; Method: single field calibrated with ESI Low Concentration Tuning Mix (Agilent)]
133.8 Ų [M+H]+
物理化学的性質
- 融点
- 56 · 56-59 °C(lit.)
- 沸点
- 174 °C · 174 °C (2.02527 mmHg)
- 比重(密度)
- 1.084 · 1.0840 (rough estimate)
- 屈折率
- 1.52 · 1.5200 (estimate)
- 闪点
- 255 °C · 255 °C
- 貯蔵温度
- Keep in dark place,Sealed in dry,Room Temperature
- 溶解性
- 0.1 g/mL、透明 · メタノール: 0.1 g/mL、透明
- 酸解離定数(Pka)
- 15.16 · 15.16±0.10(Predicted)
- 外見
- 結晶塊、結晶、フレークまたは粉末
- 色
- オフホワイトからブラウン
- 水溶解度
- 10 G/L · 10 G/L (20℃)
- Merck
- 14 · 14,9798
- BRN
- 125553 · 125553
- InChI
- 1S/C10H11NO/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12H,5-6H2
- InChIKey
- MBBOMCVGYCRMEA-UHFFFAOYSA-N
- SMILES
- OCCc1c[nH]c2ccccc12
- LogP
- 1.28 · 1.280 (est)
- CAS データベース
- 526 · 526-55-6(CAS DataBase Reference)
- NISTの化学物質情報
- 1 H-indole-3-ethanol · 1H-indole-3-ethanol(526-55-6)
- EPAの化学物質情報
- 1 H-Indole-3-ethanol · 1H-Indole-3-ethanol (526-55-6)
化学的性質
化学的特性3-(2-Hydroxyethyl)indole [526-55-6], tryptophol, C10H11NO, Mr 161.20, mp 59 ℃, bp 174 ℃, (2 kPa) forms colorless prisms or flakes that are readily soluble in methanol, ethanol, diethyl ether, chloroform, and acetone, soluble in benzene, and slightly soluble in water. It is produced by reacting methyl-1H-indole-3-acetate with lithium aluminum hydride, or through reduction of methyl-1H-indole-3-glyoxylate with sodium borohydride. The antihypertensive Indoramin is produced from tryptophol.
安全と法規制
GHS分類
GHS Classification
This chemical does not meet GHS hazard criteria for 50% (2 of 4) of reports.
Warning
H302 (25%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 4 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
安全データ
- F
- 8
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- KL3685000
- 毒性
- LD50 intraperitoneal in mouse: 351mg/kg
- hs_code
- 29339990
- 化審法
- (5)-5571
- hazard_code
- Xi
- hazard_note
- Irritant
- safety_code
- 24/25
- ストレージクラス
- 11 - Combustible Solids
化学と産業
用途と製造
応用分野
使用Tryptophol is a metabolite formed in the liver after disulfiram treatment that induces sleep in humans. It is also a secondary product of alcoholic fermentation.
調製方法
純化方法Crystallise it from diethyl ether/pet ether, *C6H6, *C6H6/pet ether. The picrate has m 100-101o (from *C6H6). [Beilstein 21 I 218, 21 II 49, 21 III/IV 788, 21/3 V 61.]
上流・下流製品情報
上流原料
サプライヤー50 社
補足説明
定義ChEBI: An indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2.
関連反応
関連ノート
読み込み中…