(2H2)Formaldehyde

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Names

[ CAS No. ]:
1664-98-8

[ Name ]:
(2H2)Formaldehyde

[Synonym ]:
d2-formaldehyde
Dideuteroparaformaldehyde
Formaldehyde-d2 polymer
formaldehyde-d2
Formaldehyde-d
Paraformaaldehyde-d6
EINECS 216-775-5
(H)Formaldehyde
Formalin-d2
MFCD00144373
perdeuteroformaldehyde
Formaldehyde-d2 solution
Formaldehyde (13C, 99%; D2, 98%)

Chemical & Physical Properties

[ Density]:
0.7±0.1 g/cm3

[ Boiling Point ]:
-19.5±9.0 °C at 760 mmHg

[ Molecular Formula ]:
CD2O

[ Molecular Weight ]:
32.038

[ Flash Point ]:
-75.1±13.7 °C

[ Exact Mass ]:
32.023117

[ PSA ]:
17.07000

[ LogP ]:
0.35

[ Vapour Pressure ]:
3463.8±0.0 mmHg at 25°C

[ Index of Refraction ]:
1.235

MSDS

Safety Information

[ Symbol ]:

GHS05, GHS07, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H302 + H312 + H332-H315-H317-H318-H334-H351

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338-P342 + P311

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
20/21/22-36/37/38-40-43

[ Safety Phrases ]:
26-36/37-51

[ RIDADR ]:
UN 3334

[ WGK Germany ]:
-

Synthetic Route

Precursor & DownStream

Precursor

  • (2H3)Methanol
  • Methanol-d4
  • 2,4,6-trichloro-N,N-bis(dideuteriomethyl)aniline
  • dideuterio-hydroxy-methyl
  • 2-Butenedioic acid,2,3-dihydroxy-, (2E)-
  • Formaldehyde
  • 1,2-(2H4)Ethanediol
  • ethylene-d4 oxide

DownStream

  • Sodium (2H)formate
  • (2H12)-1,3,5,7-Tetraazatricyclo[3.3.1.13,7]decane
  • N,N-Dimethyl(2H)formamide
  • (2H2)Methanol
  • (2H3)Methanol
  • 1,1,3,3-tetradeuterio-2,2-bis[dideuterio(hydroxy)methyl]propane-1,3-diol
  • methyl formate
  • Methyl (2H)formate
  • Thymidine-d3
  • trimethyl-d8-amine

Articles

Phosphorylation of ubiquitin at Ser65 affects its polymerization, targets, and proteome-wide turnover.

EMBO Rep. 16 , 1131-44, (2015)

Ubiquitylation is an essential post-translational modification that regulates numerous cellular processes, most notably protein degradation. Ubiquitin can itself be phosphorylated at nearly every seri...

A bead-based cleavage method for large-scale identification of protease substrates.

Sci. Rep. 6 , 22645, (2016)

Proteolysis is a major form of post translational modification which occurs when a protease cleaves peptide bonds in a target protein to modify its activity. Tracking protease substrates is indispensa...


More Articles


Related Compounds

  • (2H2)Formaldehyde
  • (2H2)Amino
  • (2H2)Aniline
  • (2H2)Sulfuric acid-(2H4)hydrazine (1:1)
  • (2H2)Formic acid
  • (2H2)Sulfuric acid
  • 1-(5-chloro-2-methoxyphenyl)-3-(2,8-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-3-yl)urea
  • 2-(benzo[d][1,3]dioxol-5-yloxy)-N-(2,7-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-3-yl)propanamide
  • 1-(3-chlorophenyl)-3-(2,7-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-3-yl)urea
  • 1-(2,7-dimethyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-3-yl)-3-(thiophen-2-yl)urea
  • N-((6-(p-tolyl)-2,3-dihydroimidazo[2,1-b]thiazol-5-yl)methyl)benzamide
  • N-(3,3-dimethyl-4-oxo-5-propyl-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-8-yl)tetrahydrofuran-2-carboxamide
  • N-(3,3-dimethyl-4-oxo-5-propyl-2,3,4,5-tetrahydrobenzo[b][1,4]oxazepin-8-yl)benzamide
  • 4-((5-oxo-5H-[1,3,4]thiadiazolo[2,3-b]quinazolin-2-yl)amino)-N-(4-(trifluoromethyl)benzyl)benzamide
  • 3-cyclopentyl-2-(((5-methyl-2-(m-tolyl)oxazol-4-yl)methyl)thio)benzofuro[3,2-d]pyrimidin-4(3H)-one
  • 2-(((2-(4-chlorophenyl)-5-methyloxazol-4-yl)methyl)thio)-3-cyclopentylbenzofuro[3,2-d]pyrimidin-4(3H)-one
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