175641
Acetic anhydride-d6
99 atom % D
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About This Item
Linear Formula:
(CD3CO)2O
CAS Number:
Molecular Weight:
108.13
UNSPSC Code:
12352103
NACRES:
NA.13
PubChem Substance ID:
EC Number:
240-697-0
Beilstein/REAXYS Number:
1910689
MDL number:
Isotopic purity:
99 atom % D
Assay:
99% (CP)
Mass shift:
M+6
Form:
liquid
SMILES string
[2H]C([2H])([2H])C(=O)OC(=O)C([2H])([2H])[2H]
InChI key
WFDIJRYMOXRFFG-WFGJKAKNSA-N
InChI
1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3/i1D3,2D3
isotopic purity
99 atom % D
assay
99% (CP)
form
liquid
technique(s)
protein expression: suitable
refractive index
n20/D 1.3875 (lit.)
bp
138-140 °C (lit.)
mp
-73 °C (lit.)
density
1.143 g/mL at 25 °C
mass shift
M+6
Quality Level
Related Categories
General description
Acetic anhydride-d6 99 atom % D is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.
Application
- NMR spectroscopy solvent for biomolecular structure analysis
- Neutron scattering experiments in materials science
- metabolic labeling studies in biological research
- Analytical method development
- Neutron scattering experiments in materials science
- metabolic labeling studies in biological research
- Analytical method development
Features and Benefits
Features
- Ideal for Advanced mass spectrometry applications
- Enhances sensitivity in analytical techniques
- Supports high-throughput analysis in research
- Safe and effective for laboratory use
Benefits
- Increases sensitivity in mass spectrometry techniques
- Provides valuable insights for pharmacokinetic research
- Enhances understanding of protein interactions
- Supports innovative research in structural biology
- Ideal for Advanced mass spectrometry applications
- Enhances sensitivity in analytical techniques
- Supports high-throughput analysis in research
- Safe and effective for laboratory use
Benefits
- Increases sensitivity in mass spectrometry techniques
- Provides valuable insights for pharmacokinetic research
- Enhances understanding of protein interactions
- Supports innovative research in structural biology
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
120.2 °F - closed cup
flash_point_c
49 °C - closed cup
Regulatory Information
危险化学品
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Mario Thevis et al.
Rapid communications in mass spectrometry : RCM, 31(14), 1175-1183 (2017-04-26)
Selective androgen receptor modulators (SARMs) represent an emerging class of therapeutics targeting inter alia conditions referred to as cachexia and sarcopenia. Due to their anabolic properties, the use of SARMs is prohibited in sports as regulated by the World Anti-Doping
Chuqiao Zhang et al.
Nucleic acids research, 48(13), 7532-7544 (2020-06-06)
Escherichia coli ItaT toxin reportedly acetylates the α-amino group of the aminoacyl-moiety of Ile-tRNAIle specifically, using acetyl-CoA as an acetyl donor, thereby inhibiting protein synthesis. The mechanism of the substrate specificity of ItaT had remained elusive. Here, we present functional
Brendan M O'Leary et al.
The Biochemical journal, 477(19), 3885-3896 (2020-09-23)
Multiple studies have shown ribulose-1,5-bisphosphate carboxylase/oxygenase (E.C. 4.1.1.39; Rubisco) to be subject to Lys-acetylation at various residues; however, opposing reports exist about the biological significance of these post-translational modifications. One aspect of the Lys-acetylation that has not been addressed in
Yuta Kawasaki et al.
International journal of biological macromolecules, 82, 772-779 (2015-10-16)
Thiothrix fructosivorans forms a microtube (sheath) that encloses a line of cells. This sheath is an assemblage of [→4)-GlcN-(1→4)-Glc-(1→]n with side chains of Rha4N-(1→3)-Fuc(1→ at position 3 of Glc. The sheath-forming polysaccharide (SFP) may have some substitutions but this is
Yuka Yashiro et al.
Nature communications, 11(1), 5438-5438 (2020-10-30)
Toxin-antitoxin systems in bacteria contribute to stress adaptation, dormancy, and persistence. AtaT, a type-II toxin in enterohemorrhagic E. coli, reportedly acetylates the α-amino group of the aminoacyl-moiety of initiator Met-tRNAfMet, thus inhibiting translation initiation. Here, we show that AtaT has
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