CAS 949092-65-3

Formula: C17H23NO4

InChI: InChI=1S/C17H23NO4/c1-18-12-7-13(9-15(18)16(20)8-12)22-17(21)14(10-19)11-5-3-2-4-6-11/h2-6,12-16,19-20H,7-10H2,1H3/t12-,13-,14-,15+,16?/m1/s1

InChI key: WTQYWNWRJNXDEG-YFVFXCHESA-N

SMILES: CN1[C@@H]2C[C@H](C[C@H]1C(C2)O)OC(=O)[C@H](CO)C3=CC=CC=C3

(1S,3R,5S)-6-Hydroxy-8-methyl-8-azabicyclo[3.2.1]oct-3-yl (αS)-α-(hydroxymethyl)benzeneacetate

CAS: 949092-65-3

(1S,3R,5S)-6-Hydroxy-8-methyl-8-azabicyclo[3.2.1]oct-3-yl (αS)-α-(hydroxymethyl)benzeneacetate

Formula: C₁₇H₂₃NO₄

Purity: 98%

Molecular weight: 305.37

Ref: 54-OR1140453

Atropine EP Impurity E (Mixture of Diastereomers) (7-Hydroxyhyoscyamine)

CAS: 949092-65-3

Formula: C₁₇H₂₃NO₄

Molecular weight: 305.38

Ref: 4Z-A-151003

Atropine EP Impurity E

CAS: 949092-65-3

Formula: C₁₇H₂₃NO₄

Molecular weight: 305.37

Ref: ST-EA-CP-A206005

7-Hydroxyhyoscyamine

CAS: 949092-65-3

7-Hydroxyhyoscyamine is an antibacterial agent that is used in the treatment of bacterial infections. It has been shown to inhibit the growth of a number of bacteria including Staphylococcus aureus, Streptococcus pyogenes, and Escherichia coli. 7-Hydroxyhyoscyamine has been shown to be more potent than 6-hydroxyhyoscyamine (6-OH Hya) for inhibiting protein synthesis in the bacteria. The compound does not have any psychoactive effects, unlike atropine sulfate, which is also an alkaloid found in plants from the Solanaceae family. 7-Hydroxyhyoscyamine can be synthesized by reacting atropine with nitrous acid or hydrochloric acid. This synthetic process leads to n-oxides as impurities, which can be removed by using a reversed phase high performance liquid chromatography (RP HPLC). Validation of this

Formula: C₁₇H₂₃NO₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 305.4 g/mol

Ref: 3D-IH171348