175641
乙酸酐-d6
99 atom % D
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关于此项目
线性分子式:
(CD3CO)2O
CAS Number:
分子量:
108.13
Beilstein:
1910689
EC 号:
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.13
同位素纯度
99 atom % D
质量水平
方案
99% (CP)
表单
liquid
技术
protein expression: suitable
折射率
n20/D 1.3875 (lit.)
沸点
138-140 °C (lit.)
mp
-73 °C (lit.)
密度
1.143 g/mL at 25 °C
质量偏移
M+6
SMILES字符串
[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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应用
- 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
特点和优势
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
包装
该产品可以大包装形式供货，也可按需进行包装。有关定价、供货和包装的信息，请联系稳定同位素客户服务。
警示用语：
Danger
危险分类
Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
120.2 °F - closed cup
闪点(°C)
49 °C - closed cup
法规信息
危险化学品
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
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
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