Cas no 2392-61-2 (L-Alanyl-L-alanine)

L-Alanyl-L-alanine structure

Product Name:L-Alanyl-L-alanine

CAS No:2392-61-2

MF:C₆H₁₂N₂O₃

MW:160.171081542969

CID:42879

PubChem ID:5484352

Update Time:2025-04-18

L-Alanyl-L-alanine Chemical and Physical Properties

Names and Identifiers

- L-Alanyl-L-alanine
- H-ALA-ALA-OH
- ALA-ALA
- Alanine, N-L-alanyl-, L-
- alpha-Alanylalanine
- Dialanine
- L-Alanine, N-L-alanyl-
- L-ALANYL-L-ALANINE extrapure
- N-L-alanyl-L-alanine
- Alanine,N-L-alanyl-, L- (8CI)
- Di-L-alanine
- a-Alanylalanine
- NSC 89598
- .alpha.-Alanylalanine
- NSC-89598
- DTXSID00173127
- MY4X7L3WAM
- EN300-865782
- SCHEMBL159553
- CHEMBL17697
- L-Alanyl-L-alanine, United States Pharmacopeia (USP) Reference Standard
- (2S)-2-[[(2S)-2-aminopropanoyl]amino]propanoic acid
- Ala-Ala-OH
- A-A Dipeptide
- UNII-37AOH3N58S
- 2392-61-2
- Alanyl-alanine
- L-Ala-L-Ala
- D86848
- (2S)-2-{[(2S)-2-aminopropanoyl]amino}propanoic acid
- Alanine Alanine dipeptide
- N-(2-Aminopropanoyl)alanine. (L)-
- UNII-MY4X7L3WAM
- D-Alanyl-D-alanine, (+/-)-
- 37AOH3N58S
- AKOS010420276
- Alanine-Alanine dipeptide
- (S)-2-((S)-2-Aminopropanamido)propanoic acid
- BDBM50016695
- NS00014576
- D-Alanine, D-alanyl-, rel-
- AS-56749
- AA dipeptide
- bmse000403
- Alanine, alanyl-
- l-Alanine N-l-alanyl
- 1948-31-8
- 1644661-10-8
- (S)-2-((S)-2-Amino-propionylamino)-propionic acid
- (2S)-2-[(2S)-2-aminopropanamido]propanoic acid
- DF49DD8A-D390-4F75-8C8A-3A07EF07DD48
- L-ALANYL-L-ALANINE [USP-RS]
- CHEBI:72816
- CS-W010878
- L-Alanine, L-alanyl-
- Q27140163
- AKOS015840020
- MFCD00008075
- EINECS 217-751-7
- 124: PN: WO2006024694 SEQID: 124claimed protein
- H-Ala-Ala-OH (L-Alanyl-L-alanine; Ala-Ala)
- HY-W010162
- Ala-Ala hydrochlorde
- FA47663
- Inchi： 1S/C6H12N2O3/c1-3(7)5(9)8-4(2)6(10)11/h3-4H,7H2,1-2H3,(H,8,9)(H,10,11)/t3-,4-/m0/s1
- InChI Key： DEFJQIDDEAULHB-IMJSIDKUSA-N
- SMILES： O=C([C@H](C)N)N[C@H](C(=O)O)C

Computed Properties

Exact Mass: 160.08479225g/mol
Monoisotopic Mass: 160.08479225g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 4
Heavy Atom Count: 11
Rotatable Bond Count: 3
Complexity: 169
Covalently-Bonded Unit Count: 1
Defined Atom Stereocenter Count: 2
Undefined Atom Stereocenter Count : 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
XLogP3: -3.3
Topological Polar Surface Area: 92.4?2

Experimental Properties

Melting Point: 286-288 oC
LogP: -3.38

L-Alanyl-L-alanine Security Information

Safety Instruction： S24/25:Prevent skin and eye contact.

L-Alanyl-L-alanine Suppliers

Suzhou Senfeida Chemical Co., Ltd

Gold Member

Audited Supplier

(CAS:2392-61-2)L-Alanyl-L-alanine

Order Number:sfd20423

Stock Status:in Stock

Quantity:200kg

Purity:99.9%

Pricing Information Last Updated:Friday, 19 July 2024 14:38

Price ($):discuss personally

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Product Official Link

L-Alanyl-L-alanine Related Literature

1. Selective complexation of α-amino acids and simple peptides via their carboxylate groups

Roland Schnitter,Daniel Gallego,Berthold Kersting Dalton Trans. 2014 43 13637
2. Melting properties of peptides and their solubility in water. Part 1: dipeptides based on glycine or alanine

Hoang Tam Do,Yeong Zen Chua,Jonas Habicht,Marcel Klinksiek,Moritz Hallermann,Dzmitry Zaitsau,Christoph Schick,Christoph Held RSC Adv. 2019 9 32722
3. Synthesis of peptides analogous to the N-terminal eicosapeptide sequence of ribonuclease A. Part II. Synthesis of the Orn10-dodecapeptide analogue of the sequence 1–12

Raniero Rocchi,Fernando Marchiori,Angelo Scatturin,Ernesto Scoffone J. Chem. Soc. C 1967 86
4. Synthesis of peptides analogous to the N-terminal eicosapeptide sequence of ribonuclease A. Part III. A new synthesis of the C-terminal octapeptide 13–20

Fernando Marchiori,Raniero Rocchi,Luigi Moroder,Giorgio Vidali,Ernesto Scoffone J. Chem. Soc. C 1967 89
5. Synthesis of peptides analogous to the N-terminal eicosapeptide of ribonuclease A. Part IV. Synthesis of the enzymatically active Orn10 and Orn10, Glu11-eicosapeptides

Ernesto Scoffone,Raniero Rocchi,Fernando Marchiori,Armando Marzotto,Angelo Scatturin,Antonmario Tamburro,Giorgio Vidali J. Chem. Soc. C 1967 606

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