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Albizziin

Product Name
Albizziin
CAS No.
1483-07-4
Chemical Name
Albizziin
Synonyms
ALBIZZIN;ALBIZZIIN;Albizzine;NSC 132089;L-ALBIZZIIN;L-ALBIZZINE;Albizziine.;L-ALBIZZIINE;Albizziin,98%;H-ALA(UREIDO)-OH
CBNumber
CB2212791
Molecular Formula
C4H9N3O3
Formula Weight
147.13
MOL File
1483-07-4.mol
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Albizziin Property

Melting point:
217°C (dec.)
alpha 
-23.4 º (c=1, 1M HCl)
Boiling point:
267.22°C (rough estimate)
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)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
Hazard Note 
Irritant
HS Code 
2937190000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
A512000
Product name
L-Albizziin
Packaging
1g
Price
$295
Updated
2021/12/16
Usbiological
Product number
A1263-01
Product name
L-Albizziin
Packaging
100mg
Price
$319
Updated
2021/12/16
SynQuest Laboratories
Product number
4157-1-W3
Product name
(2S)-(-)-2-Amino-3-(carbamoylamino)propanoic acid
Packaging
250mg
Price
$316
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA17261
Product name
L-Albizziin
Packaging
100mg
Price
$50
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA17261
Product name
L-Albizziin
Packaging
250mg
Price
$75
Updated
2021/12/16
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Albizziin Chemical Properties,Usage,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

Definition

ChEBI: L-Albizziine is a non-proteinogenic L-alpha-amino acid.

Albizziin Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Albizziin manufacturers

Career Henan Chemical Co
Product
Albizziin 1483-07-4
Price
US $3.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
100KG
Release date
2020-02-05

1483-07-4, AlbizziinRelated Search:


  • 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-ALBIZZIIN
  • 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
  • (2S)-2-ammonio-3-(carbamoylamino)propanoate
  • Albizziin USP/EP/BP
  • (S)-2-Amino-3-ureidopropanoic acid
  • 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