基本情報
- 標準SMILES
C[C@@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)NC1C(C)(C)SC1(C)C- InChIKey
IVBOUFAWPCPFTQ-SFYZADRCSA-N- 分子式
- C14H25N3O4S
- 平均分子量
- 331.43 g/mol
- 単同位体質量
- 331.15657746
名称と識別子
- 優先名称
- Alitame (Parent)
- IUPAC
- (3S)-3-amino-4-oxo-4-[[(2R)-1-oxo-1-[(2,2,4,4-tetramethylthietan-3-yl)amino]propan-2-yl]amino]butanoic acid
- 現地名
- アリターム
- 英語名
- Alitame
- 分子式
- C14H25N3O4S
- 分子量
- 331.43
名称と別名
名称をさらに表示
データベース識別子
- CAS
80863-62-3- PubChem CID
- 64763
- DTXSID
DTXSID3043780- ChEBI
CHEBI:184021- UNII
- PCE8DAE750
- Nikkaji
- J997.311G
物性
構造計算による物性
- XLogP
- -2.6
- 極性表面積
- 147 Ų
- 水素結合供与体数
- 4
- 水素結合受容体数
- 6
- 回転可能結合数
- 6
- 重原子数
- 22
- 形式電荷
- 0
- 複雑度
- 465
物理化学的性質
- 融点
- 136 · 136-147°
- 比旋光度
- 25 · D25 +40 to +50° (c = 1 in water)
- 沸点
- 608.5 · 608.5±55.0 °C(Predicted)
- 比重(密度)
- 1.25 · 1.25±0.1 g/cm3(Predicted)
- 溶解性
- Methanol (Slightly)
- 外見
- Solid
- 酸解離定数(Pka)
- 3.71 · 3.71±0.10(Predicted)
- 色
- White to Off-White
- 臭い (Odor)
- 無臭
- においのタイプ
- 無臭
- InChI
- InChI=1/C14H25N3O4S/c1-7(16-11(21)8(15)6-9(18)19)10(20)17-12-13(2,3)22-14(12,4)5/h7-8,12H,6,15H2,1-5H3,(H,16,21)(H,17,20)(H,18,19)/t7-,8+/s3
- InChIKey
- IVBOUFAWPCPFTQ-WWXSATIUNA-N
- SMILES
- N(C1C(C)(C)SC1(C)C)C(=O)[C@@H](C)NC(=O)[C@@H](N)CC(=O)O |&1:11,16,r|
- LogP
- 1.508 · 1.508 (est)
- CAS データベース
- 80863 · 80863-62-3
化学的性質
化学的特性Alitame is a white nonhygroscopic crystalline powder; odorless or having a slight characteristic odor.
安全と法規制
安全データ
- hs_code
- 29400090
化学と産業
応用分野
来歴Alitame, L-α-aspartyl-D-alanine N-(2,2,4,4-tetra methylthietan-3-yl)amide (5), was developed by Pfizer, but is owned by Danisco now. In 1986, Pfizer filed a food additive petition with the FDA. As of 2006, it was still pending. Alitame was approved for use as a sweetener by Australia in 1993, by China, Mexico, and New Zealand in 1994, by Indonesia in 1995, and by Colombia in 1996.
使用Alitame is a dipeptide amide derivative of aspartic acid used as an artificial sweetener. Alitame is about ten times sweeter than Aspartame (A790015) with a half life about twice as long.
調製方法
Alitame may be synthesized by a number of routes.For example, 3-(D-alaninamido)-2,2,4,4-tetramethylthietane is dissolved in water and L-aspartic acid N-thiocarboxyanhydride is then added in portions with vigorous stirring, maintaining the pH of 8.5–9.5. The pH is then adjusted to 5.5 and p-toluenesulfonic acid monohydrate is added over a period of one hour. The precipitated crystalline p-toluenesulfonate salt is collected by filtration. To obtain alitame from its salt, a mixture of Amberlite LA-1 (liquid anion exchange resin), dichloromethane, deionized water, and the salt is stirred for one hour, resulting in two clear layers. The aqueous layer is treated with carbon, clarified by filtration, and cooled to crystallize alitame. Alternatively, tetramethylthietane amine is condensed with anNprotected form of D-alanine to give alanyl amide. This is then coupled to a protected analogue of L-aspartic acid to give a crude form of alitame. The crude product is then purified.
上流・下流製品情報
上流原料
サプライヤー50 社
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