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Merck
CN

151777

Acetic acid-d

99 atom % D

Synonym(s):

mono-Deuteroacetic acid, Acetic (acid-d), Monodeuteroacetic acid

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About This Item

Linear Formula:
CH3COOD
CAS Number:
758-12-3
Molecular Weight:
61.06
UNSPSC Code:
12142201
NACRES:
NA.21
PubChem Substance ID:
24849163
EC Number:
212-059-1
Beilstein/REAXYS Number:
1739249
MDL number:
MFCD00051050
Assay:
99% (CP)
Form:
liquid

Key Documents

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InChI key

QTBSBXVTEAMEQO-DYCDLGHISA-N

InChI

1S/C2H4O2/c1-2(3)4/h1H3,(H,3,4)/i/hD

SMILES string

[2H]OC(C)=O

vapor density

2.07 (vs air)

vapor pressure

11.4 mmHg

isotopic purity

99 atom % D

assay

99% (CP)

form

liquid

expl. lim.

4-19.9 % (lit.)

technique(s)

NMR: suitable

impurities

≤0.50% water
water

bp

116-117 °C (lit.)

mp

15-16 °C (lit.)

density

1.059 g/cm3 at 25 °C

mass shift

M+1

Quality Level

100

Related Categories

General description

Acetic acid-d (Monodeuteroacetic acid) is the monodeuterated form of acetic acid, in which the hydrogen atom of hydroxyl group has been replaced by deuterium (D). Infrared spectral studies of its vapors at 150°C in the range of 2-25μ have been reported.

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H226,H314

Hazard Classifications

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

104.0 °F - closed cup

flash_point_c

40 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
美国出口管控产品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9017
MKCW7946
MKCT4236
MKCS5927
MKCP6350

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Vennela Mullangi et al.
Biochemistry, 51(36), 7202-7208 (2012-08-21)
We report a method for expressing the solvent accessibility of histidine imidazole groups in proteins. The method is based on measuring the rate of the hydrogen exchange (HX) reaction of the imidazole C(ε1)-hydrogen. The rate profile of the HX reaction
Infrared Investigation of Acetic Acid and Acetic Acid-d Vapors and a Vibrational Assignment for the Monomeric Acids.
Wilmshurst JK.
J. Chem. Phys. , 25(6), 1171-1173 (1956)
Li-Min Peng et al.
PeerJ, 4, e1519-e1519 (2016-01-21)
According to myosatellite cell lines (MSCs) established in vitro from diploid and triploid flounder, we compared the characters of growth and differentiation of their MSCs. The results would be useful for learning the muscle development mechanism in teleosts. The skeletal
B R Miller et al.
Neuroscience, 153(1), 329-337 (2008-03-21)
The striatum, which processes cortical information for behavioral output, is a key target of Huntington's disease (HD), an autosomal dominant condition characterized by cognitive decline and progressive loss of motor control. Increasing evidence implicates deficient glutamate uptake caused by a

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