82810-44-4 Gonyautoxin VI Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))- Gonyautoxin-VI Carbamoyl-N-sulfoneo-STX Carbamoyl-N-sulfoneosaxitoxin Gonyautoxin 6 GTX VI GTX6 N-Sulfocarbamoylneosaxitoxin Protogonyaulax Toxin B2 Toxin B 2 from Protogonyaulax Toxin B2 CAS 82810-44-4

Purity 97%+In StockPharmaceutical Standards
CAS No.82810-44-4
Molecular FormulaC10H17N7O8S
Molecular Weight395.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

82810-44-4
Gonyautoxin VI
Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))-
Gonyautoxin-VI
Carbamoyl-N-sulfoneo-STX
Carbamoyl-N-sulfoneosaxitoxin
Gonyautoxin 6
GTX VI
GTX6
N-Sulfocarbamoylneosaxitoxin
Protogonyaulax Toxin B2
Toxin B 2 from Protogonyaulax
Toxin B2 CAS 82810-44-4 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 395.35 g/mol gives 82810-44-4 Gonyautoxin VI Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))- Gonyautoxin-VI Carbamoyl-N-sulfoneo-STX Carbamoyl-N-sulfoneosaxitoxin Gonyautoxin 6 GTX VI GTX6 N-Sulfocarbamoylneosaxitoxin Protogonyaulax Toxin B2 Toxin B 2 from Protogonyaulax Toxin B2 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

82810-44-4 Gonyautoxin VI Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))- Gonyautoxin-VI Carbamoyl-N-sulfoneo-STX Carbamoyl-N-sulfoneosaxitoxin Gonyautoxin 6 GTX VI GTX6 N-Sulfocarbamoylneosaxitoxin Protogonyaulax Toxin B2 Toxin B 2 from Protogonyaulax Toxin B2 (CAS 82810-44-4), molecular formula C10H17N7O8S and molecular weight 395.35 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 82810-44-4 Gonyautoxin VI Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))- Gonyautoxin-VI Carbamoyl-N-sulfoneo-STX Carbamoyl-N-sulfoneosaxitoxin Gonyautoxin 6 GTX VI GTX6 N-Sulfocarbamoylneosaxitoxin Protogonyaulax Toxin B2 Toxin B 2 from Protogonyaulax Toxin B2 (C10H17N7O8S) contains a carbohydrate-derived structure, an amide group, a sulfone group. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 395.35 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 82810-44-4 Gonyautoxin VI Carbamic acid, sulfo-, C-((2-amino-3a,4,5,6,9,10-hexahydro-5,10,10-trihydroxy-6-imino-1H,8H-pyrrolo(1,2-c)purin-4-yl)methyl) ester, (3aS-(3aalpha,4alpha,10aR*))- Gonyautoxin-VI Carbamoyl-N-sulfoneo-STX Carbamoyl-N-sulfoneosaxitoxin Gonyautoxin 6 GTX VI GTX6 N-Sulfocarbamoylneosaxitoxin Protogonyaulax Toxin B2 Toxin B 2 from Protogonyaulax Toxin B2 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC10H17N7O8S
Molecular Weight395.35 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1980
Nitrogen Atoms7
Sulfur Atoms1

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