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Acetyl coenzyme A sodium salt - 90%, high purity , CAS No.102029-73-2

1 Citations

≥90%

CAS#: 102029-73-2
Formula: C₂₃H₃₈N₇O₁₇P₃S·xNa
Molecular Weight: 809.57（free）
MDL number: MFCD00078858
PubChem CID: 16218868

Item Number

A463299

Grouped product items
SKU	Size	Availability	Price	Qty
A463299-1mg	1mg	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$198.90
A463299-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$733.90

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Coenzymes

Basic Description

Synonyms	Acetyl CoA \| Acetyl-S- CoA
Specifications & Purity	≥90%
Biochemical and Physiological Mechanisms	Acetyl-CoA is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. It is formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degra
Storage Temp	Store at -20°C
Shipped In	Ice chest + Ice pads
Product Description	Description Acetyl-CoA is an essential cofactor and carrier of acyl groups in enzymatic acetyl transfer reactions. Acetyl CoA is formed either by the oxidative decarboxylation of pyruvate in mitochondria, by the oxidation of long-chain fatty acids, or by the oxidative degradation of certain amino acids. Acetyl-CoA is the starting compound for the citric acid cycle (Krebs cycle). Acetyl CoA is also a key precursor in lipid biosynthesis, and the source of all fatty acid carbons. Acetyl-CoA positively regulates the activity pyruvate carboxylase. Acetyl CoA is a precursor of the neurotransmitter acetylcholine. Histone acetylases (HAT) use Acetyl-CoA as the donor for the acetyl group use in the post-translational acetylation reactions of histone and non-histone proteins.An essential cofactor in enzymatic acetyl transfer reactions.

Names and Identifiers

INCHI	InChI=1S/C23H38N7O17P3S.Na/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30;/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38);
InChi Key	XGCDESRMLMCTPI-UHFFFAOYSA-N
Canonical SMILES	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.[Na]
Isomeric SMILES	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.[Na]
WGK Germany	WGK 3
Alternate CAS	72-89-9；918149-33-4
PubChem CID	16218868
Molecular Weight	809.57（free）

Certificates

Certificate of Analysis(COA)

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4 results found

Lot Number	Certificate Type	Date	Item
D2415220	Certificate of Analysis	Mar 21, 2024	A463299
D2415361	Certificate of Analysis	Mar 21, 2024	A463299
D2415362	Certificate of Analysis	Mar 21, 2024	A463299
D2415363	Certificate of Analysis	Mar 21, 2024	A463299

Chemical and Physical Properties

Solubility	H2O: 100mg/mL
Sensitivity	Moisture sensitive

Safety and Hazards(GHS)

Signal	Warning
Hazard Statements	H315:Causes skin irritation H319:Causes serious eye irritation H335:May cause respiratory irritation H302:Harmful if swallowed
Precautionary Statements	P261:Avoid breathing dust/fume/gas/mist/vapors/spray. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P302+P352:IF ON SKIN: wash with plenty of water. P301+P312:IF SWALLOWED: call a POISON CENTER/doctor/... IF you feel unwell.
WGK Germany	WGK 3
RIDADR	NONH for all modes of transport

FAQs and Articles

FAQ

The Key Molecule in Neurotransmission—Acetylcholine

Categories: Technical articles

Tags:

Metabolites Acetylcholine Nucleosides and nucleotides Coenzymes In vitro diagnostics Metabolism Neuroscience Nerve signaling

Citations of This Product

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