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Acetoacetyl coenzyme A sodium salt hydrate - ≥90%, high purity , CAS No.1420-36-6

  • ≥90%
Item Number
A341482
Grouped product items
SKUSizeAvailabilityPrice Qty
A341482-1mg
1mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$401.90
A341482-5mg
5mg
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$489.90

Discover Acetoacetyl coenzyme A sodium salt hydrate by Aladdin Scientific in ≥90% for only $401.90. Available - in Ligands at Aladdin Scientific. a substrate used by a number of enzymes including ACAT (acetoacetyl-CoA thiolase) Tags: .

Basic Description

Synonymsacetoacetyl-CoA|Acetoacetyl coenzyme A|Acetoacetyl coa|1420-36-6|3-acetoacetyl-CoA|S-Acetoacetylcoenzyme A|acetoacetyl-coenzyme a|S-Acetoacetyl-CoA|Coenzyme A, S-(3-oxobutanoate)|S-acetoacetyl-coenzyme A|acetoacetyl-S-CoA|S-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)
Specifications & Purity≥90%
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Product Description

Product Application:
Substrate for acetoacetyl-CoA thiolase EC 2.3.1.9; Role in the biosynthesis of nonactin.
Acetoacetyl coenzyme A sodium salt may be used as a substrate for a number of enzymes including; ACAT(acetoacetyl-CoA thiolase (EC 2.3.1)) which produces acetyl-CoA in reverse condensation reaction; mHMGCS and cHMGCS (3-Hydroxy-3-methylglutaryl coenzyme A (CoA) synthase (HMGCS)) which produces 3-hydroxy-3-methylglutaryl (HMG)-CoA in the mevalonate pathway leading to terpenoid biosynthesis. Acetoacetyl-CoA is also a precursor of poly-beta-hydroxybutyrate polymers in microorganisms.

Names and Identifiers

IUPAC Name S-[2-[3-[[(2R)-4-[[[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-phosphonooxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-hydroxyphosphoryl]oxy-2-hydroxy-3,3-dimethylbutanoyl]amino]propanoylamino]ethyl] 3-oxobutanethioate
INCHI InChI=1S/C25H40N7O18P3S/c1-13(33)8-16(35)54-7-6-27-15(34)4-5-28-23(38)20(37)25(2,3)10-47-53(44,45)50-52(42,43)46-9-14-19(49-51(39,40)41)18(36)24(48-14)32-12-31-17-21(26)29-11-30-22(17)32/h11-12,14,18-20,24,36-37H,4-10H2,1-3H3,(H,27,34)(H,28,38)(H,42,43)(H,44,45)(H2,26,29,30)(H2,39,40,41)/t14-,18-,19-,20+,24-/m1/s1
InChi Key OJFDKHTZOUZBOS-CITAKDKDSA-N
Canonical SMILES CC(=O)CC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O
Isomeric SMILES CC(=O)CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)O
PubChem CID 92153
Molecular Weight 851.61(anhydrous free acid basis)

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
A2426432Certificate of AnalysisJan 12, 2024 A341482
A2426433Certificate of AnalysisJan 12, 2024 A341482
A2426434Certificate of AnalysisJan 12, 2024 A341482
C2321113Certificate of AnalysisFeb 14, 2023 A341482

Chemical and Physical Properties

SolubilitySoluble in water (50 mg/ml).

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