triethylammonium phosphate

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Names

[ CAS No. ]:
10138-93-9

[ Name ]:
triethylammonium phosphate

Chemical & Physical Properties

[ Density]:
0.75g/cm3

[ Boiling Point ]:
90.5ºC at 760mmHg

[ Melting Point ]:
-114.7ºC

[ Molecular Formula ]:
C6H16NO4P

[ Molecular Weight ]:
197.16900

[ Exact Mass ]:
197.08200

[ PSA ]:
96.47000

[ LogP ]:
1.29590

[ Vapour Pressure ]:
1.97E-15mmHg at 25°C

[ Index of Refraction ]:
n20/D 1.360

[ Storage condition ]:
2-8°C

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H290-H315-H318

[ Precautionary Statements ]:
P280-P305 + P351 + P338 + P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/38

[ Safety Phrases ]:
26

[ RIDADR ]:
UN 1805 8/PG 3

[ WGK Germany ]:
1

Articles

Determination of free and total valproic acid in human plasma by capillary electrophoresis with contactless conductivity detection.

J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 907 , 74-8, (2012)

A new approach for the determination of free and total valproic acid in small samples of 140 μL human plasma based on capillary electrophoresis with contactless conductivity detection is proposed. A d...

Multifunctional thiols from the highly selective reaction of mercaptoalcohols with chlorosilanes.

Chem. Commun. (Camb.) 49(33) , 3467-9, (2013)

Multifunctional thiols were synthesized by the selective reaction of chlorosilanes with mercaptoalcohols. Reaction of the mercaptoalcohols through the thiol group was not observed. Utilizing this meth...

Synthesis of 2-nitroglycals from glycals using the tetrabutylammonium nitrate-trifluoroacetic anhydride-triethylamine reagent system and base-catalyzed Ferrier rearrangement of acetylated 2-nitroglycals.

J. Org. Chem. 78(17) , 8442-50, (2013)

A reagent system comprising tetrabutylammonium nitrate-trifluoroacetic anhydride-triethylamine has been developed for the synthesis of 2-nitroglycals from various protected glycals. The base-catalyzed...


More Articles


Related Compounds

  • Triethylammonium Phosphate
  • triethylammonium α-D-glucopyranosyl phosphate
  • triethylammonium o-iodophenyl dithiocarbamate salt
  • triethylammonium-2-N-morpholino-dithiocarbamate
  • Triethylammonium-N-pyrid-3-yl-dithiocarbamate
  • Triethylammonium-[dichloro-(2-chloro-1,3-dioxo-2-indanyl)-methanesulfonate]
  • 1-(2-Amino-3-(bromomethyl)phenyl)-3-chloropropan-2-one
  • 2-[(2r)-2-Aminopropyl]-4-fluorophenol
  • 2-[2-Amino-5-(3,4-dimethoxyphenyl)-6-(trifluoromethyl)pyrimidin-4-yl]-5-[(2-chlorobenzyl)oxy]phenol
  • 1-(3-Bromopyridin-2-yl)-2,2-difluoroethan-1-one
  • 2-(1H-1,3-benzodiazol-1-yl)ethane-1-sulfonyl chloride
  • Tert-butyl 3-carbamoyl-3-hydroxyazetidine-1-carboxylate
  • 2,2-Dimethyl-1-(2-methylphenyl)cyclopropane-1-carboxylic acid
  • 3-(Butoxymethyl)-1-methylpyrazole-4-carboxylic acid
  • 1-methyl-3-(piperidin-1-ylmethyl)-1H-pyrazole-4-carboxylic acid
  • 5-bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine-7-carboxylicacid
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