(2H2)Formaldehyde

Suppliers

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

Click to get detail 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

Click to get detail 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
  • 2,4-Dimethyl-N-[(1-methylbenzimidazol-2-yl)methyl]-6-methylsulfanylpyrimidine-5-carboxamide
  • 6-Fluoro-N-({2-[(4-methylpiperazin-1-YL)methyl]phenyl}methyl)pyridine-3-carboxamide
  • (2-Pyridin-2-ylspiro[3.3]heptan-2-yl)methanamine
  • N-[cyano(3,5-dichlorophenyl)methyl]-6-methyl-4-oxo-1,4-dihydropyridine-3-carboxamide
  • N-(8-Cyano-1,4-dioxaspiro[4.5]decan-8-yl)indolizine-2-carboxamide
  • N,2,4-Trimethyl-6-methylsulfanyl-N-[(4-methyl-1,3-thiazol-2-yl)methyl]pyrimidine-5-carboxamide
  • 4-[4-(dimethylamino)but-2-enoyl]-N-(4-methylphenyl)piperazine-1-carboxamide
  • (E)-2-(2-Chlorophenyl)-N-(2-cyanoethyl)-N-(2,2,2-trifluoroethyl)ethenesulfonamide
  • (3S)-3-(6-chloropyridin-3-yl)-3-hydroxypropanoic acid
  • Cyclohexanemethanamine, 2-[[(5-methyl-4-nitro-2-pyridinyl)oxy]methyl]-
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.