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Albizziin

Albizziin Structure
CAS No.
1483-07-4
Chemical Name:
Albizziin
Synonyms
ALBIZZIN;ALBIZZIIN;Albizzine;NSC 132089;L-ALBIZZINE;Albizziine.;L-ALBIZZIIN;L-ALBIZZIINE;Albizziin,98%;H-ALA(UREIDO)-OH
CBNumber:
CB2212791
Molecular Formula:
C4H9N3O3
Molecular Weight:
147.13
MOL File:
1483-07-4.mol
MSDS File:
SDS
Modify Date:
2024/7/26 17:49:17

Albizziin Properties

Melting point 217°C (dec.)
Boiling point 267.22°C (rough estimate)
alpha -23.4 º (c=1, 1M HCl)
Density 1.4397 (rough estimate)
refractive index 1.5700 (estimate)
storage temp. 2-8°C
solubility Methanol (Slightly), Water (Slightly)
form Solid
pka 2.15±0.10(Predicted)
color White to Off-White
Merck 13,210
CAS DataBase Reference 1483-07-4(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
Hazard Note  Irritant
HS Code  2937190000
NFPA 704
0
1 0

Albizziin Chemical Properties,Uses,Production

Chemical Properties

White powder

Uses

Albizziin is a glutamase inhibitor, a glutaminyl-tRNA synthetase inhibitor as well as an intermediate in the synthesis of heterocycles. It is also a potential effector group in affinity chromatography

Albizziin Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 103)Suppliers
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A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
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Nextpeptide Inc +86-0571-81612335 +8613336028439 China 19915 58 Inquiry
ALBIZZIIN ALBIZZIN 3-[(AMINOCARBONY)AMINO]-L-ALANINE 3-((AMINOCARBONYL)AMINO)-L-ALANINE L-(-)-2-AMINO-3-UREIDOPROPIONIC ACID L-2-AMINO-3-UREIDOPROPIONIC ACID L-ALBIZZIINE L-ALBIZZINE H-ALA(UREIDO)-OH H-BETA-(UREIDO)-ALANINE H-BETA-(UREIDO)-ALA-OH H-BETA ((AMINOCARBONYL)AMINO)-ALANINE H-BETA-((AMINOCARBONYL)AMINO)-ALA-OH Albizziine. H-beta-Ureido-Ala-OH, 2-Amino-3-ureido-L-propionic acid, 98% (2S)-2-Amino-3-(carbamoylamino)propanoic acid L-Alanine, 3-[(aminocarbonyl)amino]- L-b-Ureidoalanine Propionic acid, 2-amino-3-ureido- [R,(+)]-2-Amino-3-ureidopropionic acid 3-(Aminocarbonylamino)-D-alanine [S,(-)]-2-Amino-3-ureidopropionic acid Albizziin,98% L-Albizziin, L-(-)-2-Amino-3-ureidopropionic acid L-β-Ureidoalanine NSC 132089 H-b-((AMinocarbonyl)aMino)-Ala-OH, H-Dap(carbaMoyl)-OH H-b-(Ureido)-Ala-OH 3-[(Aminocarbony)amino]-L-alanine≥ 99% (Titration) L-(-)-2-Amino-3-uraeidopropionic acid L-Ala(ureido)-OH L-(-)-2-Amino-3-ureidopropionic acid, L-2-Amino-3-ureidopropionic acid L-ALBIZZIIN (S)-2-Amino-3-ureidopropanoic acid Albizziin USP/EP/BP (2S)-2-ammonio-3-(carbamoylamino)propanoate Albizzine L-beta-Ureidoalanine LAlbizziin,L-Albizziin,Inhibitor,L Albizziin,inhibit,reagent,Glutaminase,glutamase,group,sulfhydryl (2S)-2-amino-3-[(aminocarbony l)amino]propanoic acid 1483-07-4 C4H9N3O3 H2NCONHCH2CHNH2CO2H Peptide Synthesis Others Unnatural Amino Acid Derivatives Specialty Synthesis Amino Acids 13C, 2H, 15N Amino Acids & Derivatives Inhibitors Herpes Viruses