기본 정보
- 표준 SMILES
C[C@@H](NC(=O)[C@@H](N)CC(=O)O)C(=O)NC1C(C)(C)SC1(C)C- InChIKey
IVBOUFAWPCPFTQ-SFYZADRCSA-N- 분자식
- C14H25N3O4S
- 평균 분자량
- 331.43 g/mol
- 단동위원소 질량
- 331.15657746
이름 및 식별자
- 우선 이름
- 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
- 영어명
- Alitame
- 분자식
- C14H25N3O4S
- 분자량
- 331.43
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
80863-62-3- PubChem CID
- 64763
- DTXSID
DTXSID3043780- ChEBI
CHEBI:184021- UNII
- PCE8DAE750
- Nikkaji
- J997.311G
물성
구조 계산 물성
- XLogP
- -2.6
- 극성 표면적
- 147 Ų
- 수소 결합 공여자 수
- 4
- 수소 결합 수용자 수
- 6
- 회전 가능 결합 수
- 6
- 무거운 원자 수
- 22
- 형식 전하
- 0
- 복잡도
- 465
물리화학적 성질
- 녹는점
- 136 · 136-147°
- 끓는 점
- 608.5 · 608.5±55.0 °C(Predicted)
- 밀도
- 1.25 · 1.25±0.1 g/cm3(Predicted)
- 용해도
- 메탄올(약간)에 용해됨
- 물리적 상태
- 고체
- 산도 계수 (pKa)
- 3.71 · 3.71±0.10(Predicted)
- 색상
- 흰색에서 황백색까지
- 냄새
- 냄새 없는
- 냄새 유형
- 냄새 없는
- 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)
화학적 성질
Alitame is a white nonhygroscopic crystalline powder; odorless or having a slight characteristic odor.
안전 및 규제
안전 데이터
- HS 번호
- 29400090
화학 및 산업
응용 분야
역사Alitame, 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.
용도Alitame 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.
제조 방법
생산 방법Alitame 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.
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공급사50 곳
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