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Merck
CN

176079

Sodium acetate-d3

99 atom % D

Synonym(s):

Acetic-d3 acid sodium salt

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About This Item

Linear Formula:
CD3CO2Na
CAS Number:
Molecular Weight:
85.05
NACRES:
NA.12
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
254-366-3
MDL number:
Isotopic purity:
99 atom % D
Mass shift:
M+3
Form:
crystals
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InChI key

VMHLLURERBWHNL-NIIDSAIPSA-M

InChI

1S/C2H4O2.Na/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1/i1D3;

SMILES string

[Na+].[2H]C([2H])([2H])C([O-])=O

isotopic purity

99 atom % D

form

crystals

technique(s)

NMR: suitable, bio NMR: suitable, protein expression: suitable

mp

>300 °C (dec.) (lit.)

mass shift

M+3

Quality Level

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

美国出口管控产品
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Frederik Fleissner et al.
Advanced biosystems, 4(11), e2000111-e2000111 (2020-11-03)
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Biochimica et biophysica acta. Molecular and cell biology of lipids, 1865(6), 158666-158666 (2020-02-18)
Short-chain fatty acids (SCFAs), including acetate, butyrate, and propionate, are produced when colonic bacteria in the human gastrointestinal tract ferment undigested fibers. Free fatty acid receptor 2 (FFA2) and FFA3 are G-protein-coupled receptors recently identified as SCFA receptors that may
Will Kew et al.
Food chemistry, 298, 125052-125052 (2019-07-02)
Scotch Whisky has been analysed as a complex mixture in its raw form using high resolution Nuclear Magnetic Resonance (NMR) and previously developed water and ethanol suppression techniques. This has allowed for the positive identification of 25 compounds in Scotch
Thomas W Hoffmann et al.
The ISME journal, 10(2), 460-477 (2015-07-29)
Studying host-microbiota interactions are fundamental to understanding the mechanisms involved in intestinal homeostasis and inflammation. In this work, we analyzed these interactions in mice that were mono-associated with six microorganisms that are representative of inflammatory bowel disease (IBD)-associated dysbiosis: the
Michael A McMechen et al.
Molecules (Basel, Switzerland), 24(10) (2019-05-22)
Cα to N substitution in aza-amino acids imposes local conformational constraints, changes in hydrogen bonding properties, and leads to adaptive chirality at the nitrogen atom. These properties can be exploited in mimicry and stabilization of peptide secondary structures and self-assembly.

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