175641
Acetic anhydride-d6
99 atom % D
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About This Item
Linear Formula:
(CD3CO)2O
CAS Number:
Molecular Weight:
108.13
Beilstein:
1910689
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.13
isotopic purity
99 atom % D
Quality Level
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
SMILES string
[2H]C([2H])([2H])C(=O)OC(=O)C([2H])([2H])[2H]
InChI
1S/C4H6O3/c1-3(5)7-4(2)6/h1-2H3/i1D3,2D3
InChI key
WFDIJRYMOXRFFG-WFGJKAKNSA-N
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
Storage Class Code
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
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
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
Peter S Backlund et al.
Journal of biological rhythms, 32(3), 195-211 (2017-05-04)
Normal physiology undergoes 24-h changes in function that include daily rhythms in circulating hormones, most notably melatonin and cortical steroids. This study focused on N-acetyltryptamine, a little-studied melatonin receptor mixed agonist-antagonist and the likely evolutionary precursor of melatonin. The central
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
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