Butoxamine hydrochloride

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Names

[ CAS No. ]:
5696-15-1

[ Name ]:
Butoxamine hydrochloride

[Synonym ]:
N-tert.-Butyl-pseudomethoxaminhydrochlorid
BUTOXAMINE HYDROCHLORIDE
Butoxamine hydrochloride (USAN)
BW 64-9
Butoxamine HCl
N-tert-Butylmethoxamine hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
391ºC at 760 mmHg

[ Molecular Formula ]:
C15H26ClNO3

[ Molecular Weight ]:
303.82500

[ Flash Point ]:
190.3ºC

[ Exact Mass ]:
303.16000

[ PSA ]:
50.72000

[ LogP ]:
3.70670

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H319

[ Precautionary Statements ]:
P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn

[ Risk Phrases ]:
22-36

[ Safety Phrases ]:
26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

Restoration of neutrophil immunocompetence after cardiopulmonary bypass by beta-adrenergic blockers.

Surgery 147(4) , 562-74, (2010)

To evaluate the possible protective effect of sympatholytic medications with respect to neutrophil function, we evaluated the influence of a nonselective beta-blocker medication on the interaction of ...

Does selective beta-1 blockade provide bone marrow protection after trauma/hemorrhagic shock?

Surgery 152(3) , 322-30, (2012)

Previously, nonselective beta-blockade (BB) with propranolol demonstrated protection of the bone marrow (BM) after trauma and hemorrhagic shock (HS). Because selective beta-1 blockers are used commonl...

Blocking of beta-2 adrenergic receptors hastens recovery from hypoglycemia-associated social withdrawal.

Psychoneuroendocrinology 33(10) , 1411-8, (2008)

Hypoglycemia is associated with a variety of adverse behaviors including fatigue, confusion and social withdrawal. While these clinical symptoms are well characterized, the mechanism of their cause is...


More Articles


Related Compounds

  • butoxamine hydrochloride
  • Tyrocidine, hydrochloride
  • Triprolidine hydrochloride
  • Minoxidil hydrochloride
  • Elacridar hydrochloride
  • dodecylamine hydrochloride
  • N-(4-(2-((4-bromophenyl)amino)-2-oxoethyl)thiazol-2-yl)cyclopropanecarboxamide
  • N-(4-(2-((3-methoxybenzyl)amino)-2-oxoethyl)thiazol-2-yl)cyclopropanecarboxamide
  • N-(4-(2-oxo-2-((pyridin-4-ylmethyl)amino)ethyl)thiazol-2-yl)cyclopropanecarboxamide
  • 5-methyl-N-(4-methylbenzyl)-2,4-dioxo-3-phenyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide
  • 5-methyl-2,4-dioxo-3-phenyl-N-(3-phenylpropyl)-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide
  • N-(4-isopropylphenyl)-5-methyl-2,4-dioxo-3-phenyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide
  • (16alpha,19alpha)-19-Hydroxy-19-methyl-18-oxayohimban-16-carboxylic acid
  • 5-methyl-2,4-dioxo-3-phenyl-N-(4-(trifluoromethyl)phenyl)-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide
  • N-(3-methoxyphenyl)-5-methyl-2,4-dioxo-3-phenyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide
  • 5-methyl-2,4-dioxo-3-phenyl-N-(4-(trifluoromethoxy)phenyl)-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidine-7-carboxamide