Acute toxicity
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BETA-AMANITIN

Acute toxicity
Product Name
BETA-AMANITIN
CAS No.
21150-22-1
Chemical Name
BETA-AMANITIN
Synonyms
b-Amanitin;β-Amanitin;B-Amanitine;β-Amanitine;BETA-AMANITIN;beta-amatoxin;beta-Amanitine;β-Amanitin DISCONTINUED;1-l-asparticacid-alpha-amaniti;α-Amanitin, 1-L-aspartic acid-
CBNumber
CB0383204
Molecular Formula
C39H53N9O15S
Formula Weight
919.95
MOL File
21150-22-1.mol
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BETA-AMANITIN Property

Melting point:
300°
Boiling point:
1599.6±65.0 °C(Predicted)
Density 
1.1725 (rough estimate)
refractive index 
1.7400 (estimate)
storage temp. 
−20°C
solubility 
Water: 1 mg/ml
pka
4.02±0.10(Predicted)
form 
White to off-white powder.
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Safety

Hazard Codes 
T+
Risk Statements 
26/27/28
Safety Statements 
7-28-36/37/39-45
RIDADR 
UN 3462 6.1/PG 1
WGK Germany 
3
RTECS 
NJ8324000
HazardClass 
6.1(a)
PackingGroup 
I
HS Code 
2934999090
Toxicity
LD50 i.p. in albino mice: 0.4 mg/kg (Wieland, Wieland)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Precautionary statements

P260Do not breathe dust/fume/gas/mist/vapours/spray.

P262Do not get in eyes, on skin, or on clothing.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
A1304
Product name
β-Amanitin from Amanita phalloides
Purity
~90% (HPLC)
Packaging
1mg
Price
$865
Updated
2024/03/01
Cayman Chemical
Product number
18142
Product name
β-Amanitin
Purity
≥95%
Packaging
1mg
Price
$241
Updated
2024/03/01
Biosynth Carbosynth
Product number
FA57612
Product name
b-Amanitin
Packaging
1mg
Price
$300
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA57612
Product name
b-Amanitin
Packaging
2mg
Price
$400
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA57612
Product name
b-Amanitin
Packaging
5mg
Price
$600
Updated
2021/12/16
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BETA-AMANITIN Chemical Properties,Usage,Production

Acute toxicity

peritoneal-mouse LD50: 0.4 mg/kg; unnamed-mouse LD50: 0.4 mg/kg

Mechanism of action

β-Amanitin is a cyclic peptide found in several species of the Amanita genus, as well as other poisonous fungi. It inhibits RNA polymerase II and III but not RNA polymerase I or bacterial RNA polymerase, thus preventing mammalian protein synthesis. The biological activity of this toxin is similar to that of α-amanitin but differs structurally by the presence of a carboxyl group, which is useful for coupling reactions.

Uses

β-Amanitin from Amanita phalloides has been used:

  • as a calibration standard for the quantification of β-Amanitin using liquid chromatography-high resolution-mass spectrometry/mass spectrometry (LC-HR-MS/MS) method.
  • to determine its concentration in urine samples by capillary zone electrophoresis (CZE).
  • in the analysis of β-amanitin in toxic mushrooms by liquid chromatography coupled to time-of-flight mass spectrometry.

Uses

As a tool in molecular biology.

General Description

β-Amanitin belongs to the family of amatoxins. Amanitins are made of bicyclic octapeptides. β-Amanitin is composed of a carboxyl group and is acidic in nature.

Biochem/physiol Actions

Toxic constituent of the mushroom, Amanita phalloides, inhibits eukaryotic RNA polymerase II and III, but not RNA polymerase I or bacterial RNA polymerase. Inhibits mammalian protein synthesis.

BETA-AMANITIN Preparation Products And Raw materials

Raw materials

Preparation Products

21150-22-1, BETA-AMANITINRelated Search:


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  • Cyclo[L-Asp-L-t4Hyp-[(3R,4R)-4,5-dihydroxy-3-methyl-L-Nva-]-6-hydroxy-L-Trp2(1)-Gly-3-methyl-L-Nva-Gly-3-oxomercapto(1)-L-Ala-]
  • b-Amanitin
  • beta-Amanitin from Amanita Phalloides
  • α-Amanitin, 1-L-aspartic acid-
  • β-Amanitin
  • β-Amanitin DISCONTINUED
  • β-Amanitine
  • β-Amanitin from Amanita phalloides
  • 21150-22-1
  • C39H53N9O15S
  • DNA-RNA Transcription Regulators
  • Gene Regulation and Expression
  • BioChemical
  • Cell Signaling and Neuroscience
  • Cell Biology
  • Cell Signaling and Neuroscience
  • DNA-RNA Transcription RegulatorsCell Signaling and Neuroscience
  • Gene Regulation and Expression
  • Mushroom
  • Toxins and Venoms