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.
color 
White to off-white
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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

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BETA-AMANITIN Suppliers

Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9806
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12306
Advantage
58
Shenzhen Regent Biochemical Technology Co., Ltd.
Tel
0755-0755-85201366 18938635012
Fax
0755-85201366
Email
sales@regentsciences.com
Country
China
ProdList
9355
Advantage
58
BOC Sciences
Tel
16314854226; +16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19741
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
32165
Advantage
58
Hubei xin bonus chemical co. LTD
Tel
86-13657291602
Fax
027-59338440
Email
linda@hubeijusheng.com
Country
CHINA
ProdList
22963
Advantage
58
ChemeGen(Shanghai) Biotechnology Co.,Ltd.
Tel
18818260767
Fax
QQ 3610331285
Email
sales@chemegen.com
Country
China
ProdList
11217
Advantage
58
ShangHai Anpel Co, Ltd.
Tel
18501792038; 18501792038
Email
shanpel@anpel.com.cn
Country
China
ProdList
9611
Advantage
58

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  • DNA-RNA Transcription Regulators
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  • BioChemical
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