CAS 910138-96-4

DULOXETINE IMPURITY A CRS

CAS: 910138-96-4

DULOXETINE IMPURITY A CRS

Ref: 41-Y0001455

Duloxetine Related Compound A ((R)-N-Methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine hydrochloride)

CAS: 910138-96-4

Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoi

Fórmula: C₁₈H₁₉NOS·HCl

Cor e Forma: Off-White Solid

Peso molecular: 297.11874

Ref: 45-1229828

Duloxetine EP Impurity A Maleate (Duloxetine USP Related Compound A Maleate)

CAS: 116539-60-7, 910138-96-4

Fórmula: C₁₈H₁₉NOS·C₄H₄O₄

Cor e Forma: White To Off-White Solid

Peso molecular: 297.42 116.07

Ref: 4Z-D-1127

(3R)-N-Methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine Hydrochloride ((R)-Duloxetine Hydrochloride)

CAS: 910138-96-4

Cor e Forma: Neat

Ref: 86-MM1122.11

Duloxetine EP Impurity A

CAS: 910138-96-4

Fórmula: C₁₈H₁₉NOSHCl

Peso molecular: 297.4 : 36.46

Ref: ST-EA-CP-D29001

(R)-Duloxetine Hydrochloride

Produto Controlado

CAS: 910138-96-4

Applications A napthalenyloxy-substituted amine used in binding studies of human serum albumin along with (S)-Duloxetine (D721000). Unlike its enantiomer, it is not a very effective dual serotonin and norepinephrine reuptake inhibitor (SNRI).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Bymaster, F.P. et al.: Bioorg. Med. Chem. Lett., 13, 4477 (2003); Liu, X. et al.: Eur. J. Med. Chem., 45, 4043 (2010);

Fórmula: C₁₈H₁₉NOS·ClH

Cor e Forma: Neat

Peso molecular: 333.88

Ref: TR-D720990

(R)-N-Methyl-3-(1-naphthoxy)-3-(2-thienyl)propylamine hydrochloride

Produto Controlado

CAS: 910138-96-4

(R)-N-Methyl-3-(1-naphthoxy)-3-(2-thienyl)propylamine hydrochloride is a nonsteroidal anti-inflammatory drug that has been shown to be effective for the treatment of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and chronic low back pain. This drug can also be used for other inflammatory conditions such as psoriasis and Crohn's disease. The mechanism of action of (R)-N-Methyl-3-(1-naphthoxy)-3-(2-thienyl)propylamine hydrochloride is not fully understood. It may work by blocking the synthesis of prostaglandins in the body. This drug is metabolized in the liver to its active form, which binds to cyclooxygenase 1 and 2 enzymes to inhibit the production of prostaglandins. It also inhibits human serum x-ray

Fórmula: C₁₈H₁₉NOS•HCl

Pureza: Min. 95%

Cor e Forma: White To Off-White Solid

Peso molecular: 333.88 g/mol

Ref: 3D-FD22626

Duloxetine-d3 Oxalate

Produto Controlado

CAS: 910138-96-4

Fórmula: C₂₀H₁₈D₃NO₅S

Cor e Forma: Neat

Peso molecular: 390.47

Ref: TR-D720993

(R)-Duloxetine Hydrochloride

CAS: 910138-96-4

(R)-Duloxetine Hydrochloride, naphthalenyloxy amine, binds human serum albumin, less effective than (S)-enantiomer as SNRI.

Fórmula: C₁₈H₂₀ClNOS

Cor e Forma: Solid

Peso molecular: 333.87

Ref: TM-T68386