Skip to Content
MilliporeSigma
All Photos(1)

Documents

175641

Sigma-Aldrich

Acetic anhydride-d6

99 atom % D

Sign Into View Organizational & Contract Pricing

Linear Formula:
(CD3CO)2O
CAS Number:
Molecular Weight:
108.13
Beilstein/REAXYS Number:
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

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

wgk_germany

WGK 1

flash_point_f

120.2 °F

flash_point_c

49 °C


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 6

1 of 6

Acetyl chloride-1-13C 99 atom % 13C

Sigma-Aldrich

293156

Acetyl chloride-1-13C

Acetic acid-d4 ≥99.5 atom % D, contains 0.03 % (v/v) TMS

Sigma-Aldrich

416886

Acetic acid-d4

Acetic acid-d4 ≥99.9 atom % D

Sigma-Aldrich

233315

Acetic acid-d4

Propionic acid-d6 98 atom % D

Sigma-Aldrich

490644

Propionic acid-d6

Acetic acid-d 99 atom % D

Sigma-Aldrich

151777

Acetic acid-d

Acetic acid-2-13C 99 atom % 13C

Sigma-Aldrich

279307

Acetic acid-2-13C

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
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
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
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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service