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Merck
모든 사진(1)

주요 문서

175641

Sigma-Aldrich

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 코드:
12352103
PubChem Substance ID:
NACRES:
NA.13

동위원소 순도

99 atom % D

Quality Level

분석

99% (CP)

양식

liquid

기술

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

질량 이동

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

포장

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.

픽토그램

FlameSkull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

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


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시험 성적서(COA)

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문서 라이브러리 방문

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
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

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