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Sodium acetate - anhydrous 99.99% SuperPure grade, high purity , CAS No.127-09-3

  • anhydrous
  • PrimorTrace™
  • SuperPure grade
  • ≥99.99% metals basis
Item Number
S431683
Grouped product items
SKUSizeAvailabilityPrice Qty
S431683-50g
50g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$998.90
S431683-500g
500g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$3,475.90
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Salt

Basic Description

SynonymsSodium acetate|127-09-3|Acetic acid, sodium salt|Sodium acetate anhydrous|Acetic acid sodium salt|Sodium acetate, anhydrous|Anhydrous sodium acetate|Sodii acetas|Sodium ethanoate|Natrium aceticum|FEMA No. 3024|Natriumacetat|Octan sodny|Caswell No. 741A|FE
Specifications & PurityPrimorTrace™, anhydrous, SuperPure grade, ≥99.99% metals basis
Storage TempRoom temperature
Shipped InNormal
Gradeanhydrous, PrimorTrace™, SuperPure grade

Associated Targets

CA5A Tclin Carbonic anhydrase 5A, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

FFAR3 Tchem Free fatty acid receptor 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA1 Tclin Carbonic anhydrase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA2 Tclin Carbonic anhydrase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA4 Tclin Carbonic anhydrase 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CA9 Tclin Carbonic anhydrase 9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name sodium;acetate
INCHI InChI=1S/C2H4O2.Na/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
InChi Key VMHLLURERBWHNL-UHFFFAOYSA-M
Canonical SMILES CC(=O)[O-].[Na+]
Isomeric SMILES CC(=O)[O-].[Na+]
PubChem CID 517045
Molecular Weight 82.03

Certificates

Certificate of Analysis(COA)

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Chemical and Physical Properties

Solubility365g/L
Flash Point(°C)>250°C
Melt Point(°C)324°C

Related Documents

 SDS

 Specification Sheet

FAQs and Articles

FAQ
Aladdin@Guidelines for the formulation of commonly used buffers for biological experiments
Categories: Technical articles
Tags:
Biochemical reagents Antibiotics Western blot Stains and dyes Electrophoresis Biological buffers

References

1. zeyu shou.  (2024)  Immobilizing c(RGDfc) on the surface of metal-phenolic networks by thiol-click reaction for accelerating osteointegration of implant.  Materials Today Bio,  25  (1): (101017).  [PMID:]
2. zeyu shou.  (2024)  Immobilizing c(RGDfc) on the surface of metal-phenolic networks by thiol-click reaction for accelerating osteointegration of implant.  Materials Today Bio,  25  (1): (101017).  [PMID:]

Solution Calculators

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