All Photos(1)

Documents

B1385

Butoxamine hydrochloride

Name: Butoxamine hydrochloride
Brand: SIAL

analytical standard, for drug analysis, mixture of diastereomers

Synonym(s):

α-(1-[t-Butylamino]ethyl)-2,5-dimethoxybenzyl alcohol

Sign Into View Organizational & Contract Pricing

All Photos(1)

About This Item

Empirical Formula (Hill Notation):

C₁₅H₂₅NO₃ · HCl

CAS Number:

5696-15-1

Molecular Weight:

303.82

EC Number:

227-169-5

MDL number:

MFCD00135781

UNSPSC Code:

41116107

PubChem Substance ID:

329773182

NACRES:

NA.24

grade

analytical standard, for drug analysis

Quality Level

200

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

Cl.COc1ccc(OC)c(c1)C(O)C(C)NC(C)(C)C

InChI

1S/C15H25NO3.ClH/c1-10(16-15(2,3)4)14(17)12-9-11(18-5)7-8-13(12)19-6;/h7-10,14,16-17H,1-6H3;1H

InChI key

URPAECSKKQLCII-UHFFFAOYSA-N

Related Categories

Chromatography Standards

Controlled Substances & Illicit Drug Standards

General description

Butoxamine hydrochloride is a β-andrenoceptor antagonist, which shows β₂-selectivity.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H302,H319

Precautionary Statements

P264 - P270 - P280 - P301 + P312 - P305 + P351 + P338 - P337 + P313

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Cardiovascular teratogenicity of terbutaline and ritodrine in the chick embryo

Lenselink R.D, et al.

American Journal of Obstetrics and Gynecology, 171(2), 501-506 (1994)

The Role of the FOXO1/β2-AR/p-NF-κB p65 Pathway in the Development of Endometrial Stromal Cells in Pregnant Mice under Restraint Stress.

Jiayin Lu et al.

International journal of molecular sciences, 22(3) (2021-02-06)

Restraint stress causes various maternal diseases during pregnancy. β2-Adrenergic receptor (β2-AR) and Forkhead transcription factor class O 1 (FOXO1) are critical factors not only in stress, but also in reproduction. However, the role of FOXO1 in restraint stress, causing changes

Restraint stress induces uterine microenvironment disorder in mice during early pregnancy through the β2-AR/cAMP/PKA pathway.

Jiayin Lu et al.

Stress (Amsterdam, Netherlands), 24(5), 514-528 (2020-12-08)

During pregnancy, uterus undergoes the environment adaptation as part of a program of development. In the world, one in four people worldwide suffer from mental illness, especially pregnant women. β-Adrenergic receptor (β-AR) is an important regulator that converts environmental stimuli

Olodaterol exerts anti-inflammatory effects on COPD airway epithelial cells.

Nan Yang et al.

Respiratory research, 22(1), 65-65 (2021-02-25)

Airway inflammation is a key feature of chronic obstructive pulmonary disease (COPD) and inhaled corticosteroids (ICS) remain the main treatment for airway inflammation. Studies have noted the increased efficacy of ICS and long-acting beta 2 agonist (LABA) combination therapy in

Concise Dictionary of Pharmacological Agents: Properties and Synonyms null

View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service