CAS:551-16-6 C8H12N...

CAS:551-16-6 C8H12N2O3S 6-Aminopenicillanic acid

CAS:551-16-6 C8H12N2O3S 6-Aminopenicillanic acid

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500 Gram

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  • Min.Order :500 Gram
  • Purity: 99%
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Keywords

CAS:551-16-6 C8H12N2O3S 6-Aminopenicillanic acid CAS:551-16-6 C8H12N2O3S CAS:551-16-6

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  • Appearance:white poweder
  • Application:CAS:551-16-6 C8H12N2O3S
  • PackAge:Plastic vacuum packaging bag or bucket
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:under the cool and dry area
  • Transportation:by express or by sea

Superiority:

6-Aminopenicillanic acid Basic information
Product Name: 6-Aminopenicillanic acid
Synonyms: (25,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;(2S,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO-[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-AMINO-2,2-DIMETHYL-5-OXOPERHYDROAZETO[2,1-B][1,3]THIAZOLE-3-CARBOXYLIC ACID;6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-APA;(+)-6-AMINOPENICILLANIC ACID;6-AMINOPENICILLANIC ACID;6-AMINO PENICILLINIC ACID
CAS: 551-16-6
MF: C8H12N2O3S
MW: 216.26
EINECS: 208-993-4
Product Categories: Organic acids;Antibiotics for Research and Experimental Use;beta-Lactams (Antibiotics for Research and Experimental Use);Biochemistry;Chemical Intermediate;Used as pharmaceutical intermediates;API
Mol File: 551-16-6.mol
6-Aminopenicillanic acid Structure
 
6-Aminopenicillanic acid Chemical Properties
mp  198-200 °C (dec.)(lit.)
alpha  276.3 º (c=1.2, 0.1N HCl 22 ºC)
storage temp.  2-8°C
Merck  14,458
BRN  15080
CAS DataBase Reference 551-16-6(CAS DataBase Reference)
EPA Substance Registry System 4-Thia-1-azabicyclo[ 3.2.0]heptane-2-carboxylic acid, 6-amino-3,3-dimethyl-7-oxo-, (2S,5R,6R)-(551-16-6)
 
Safety Information
Hazard Codes  Xn
Risk Statements  42/43
Safety Statements  22-36/37-45-37-24-36
WGK Germany  2
RTECS  XH8225000
F  10
HS Code  29349990
MSDS Information
Provider Language
6-Aminopenicillanic acid English
ACROS English
SigmaAldrich English
ALFA English
 
6-Aminopenicillanic acid Usage And Synthesis
Chemical Properties WHITE TO CREAM FINE POWDER
Usage (+)-6-Aminopenicillanic Acid is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins.

 

Details:

6-Aminopenicillanic acid Basic information
Product Name: 6-Aminopenicillanic acid
Synonyms: (25,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;(2S,5R,6R)-6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO-[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-AMINO-2,2-DIMETHYL-5-OXOPERHYDROAZETO[2,1-B][1,3]THIAZOLE-3-CARBOXYLIC ACID;6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZABICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID;6-APA;(+)-6-AMINOPENICILLANIC ACID;6-AMINOPENICILLANIC ACID;6-AMINO PENICILLINIC ACID
CAS: 551-16-6
MF: C8H12N2O3S
MW: 216.26
EINECS: 208-993-4
Product Categories: Organic acids;Antibiotics for Research and Experimental Use;beta-Lactams (Antibiotics for Research and Experimental Use);Biochemistry;Chemical Intermediate;Used as pharmaceutical intermediates;API
Mol File: 551-16-6.mol
6-Aminopenicillanic acid Structure
 
6-Aminopenicillanic acid Chemical Properties
mp  198-200 °C (dec.)(lit.)
alpha  276.3 º (c=1.2, 0.1N HCl 22 ºC)
storage temp.  2-8°C
Merck  14,458
BRN  15080
CAS DataBase Reference 551-16-6(CAS DataBase Reference)
EPA Substance Registry System 4-Thia-1-azabicyclo[ 3.2.0]heptane-2-carboxylic acid, 6-amino-3,3-dimethyl-7-oxo-, (2S,5R,6R)-(551-16-6)
 
Safety Information
Hazard Codes  Xn
Risk Statements  42/43
Safety Statements  22-36/37-45-37-24-36
WGK Germany  2
RTECS  XH8225000
F  10
HS Code  29349990
MSDS Information
Provider Language
6-Aminopenicillanic acid English
ACROS English
SigmaAldrich English
ALFA English
 
6-Aminopenicillanic acid Usage And Synthesis
Chemical Properties WHITE TO CREAM FINE POWDER
Usage (+)-6-Aminopenicillanic Acid is the core structure in penicillins, obtained from the fermentation brew of the Penicillium mold. (+)-6-Aminopenicillanic Acid is used as the main starting block for the preparation of numerous semisynthetic penicillins.

 

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