CAS 3040-44-6

1-Piperidineethanol

Description:

1-Piperidineethanol, with the CAS number 3040-44-6, is an organic compound characterized by the presence of a piperidine ring and an ethanol moiety. It features a six-membered saturated nitrogen-containing heterocycle (piperidine) attached to a two-carbon alcohol chain (ethanol). This compound is typically a colorless to pale yellow liquid with a distinctive amine-like odor. It is soluble in water and organic solvents, reflecting its polar nature due to the hydroxyl (-OH) group. The presence of the piperidine ring contributes to its basicity and potential reactivity, making it a useful intermediate in organic synthesis and pharmaceuticals. Additionally, 1-Piperidineethanol may exhibit biological activity, which can be explored for various applications in medicinal chemistry. Safety data indicates that it should be handled with care, as it may cause irritation upon contact with skin or eyes. Overall, 1-Piperidineethanol is a versatile compound with significant implications in chemical research and industry.

Formula: C₇H₁₅NO

InChI: InChI=1/C7H15NO/c9-7-6-8-4-2-1-3-5-8/h9H,1-7H2/p+1

InChI key: InChIKey=KZTWONRVIPPDKH-UHFFFAOYSA-N

SMILES: C(CO)N1CCCCC1

Synonyms:

• 1-(2-Hydroxyethyl)piperidine
• 1-Piperidine ethanol
• 1-Piperidineethanol
• 2-(1-Piperidino)ethanol
• 2-(1-Piperidinyl)ethanol
• 2-(N-Piperidino)ethanol
• 2-(Piperid-1-yl)ethanol
• 2-(Piperidin-1-yl)ethan-1-ol
• 2-(Piperidine-1-yl)ethanol
• 2-Piperidinoethanol
• N-(2-hydroxyethyl)piperidine
• N-(β-Hydroxyethyl)piperidine
• N-Piperidinoethanol
• NSC 3460
• β-Piperidinoethanol
• PIPERIDINOETHANOL
• beta-Piperidylethanol
• 2-PIPERIDINETHANOL
• Piperidine, 1-(2-hydroxyethyl)
• N-HYDROXYETHYL PIPERIDINE
• beta-Piperidinoethanol
• AKOS BBS-00004365
• BUTTPARK 154\16-41
• N-PIPERIDINEETHANOL
• 1-Piperidineethanol/1-(2-Hydroxyethyl)Piperidine/2-(1-Piperidino)Ethanol
• N-2-HydroxyEthylPiperidin
• 1-PIPERIDINOETHANOL

1-Piperidineethanol

CAS: 3040-44-6

Formula: C₇H₁₅NO

Purity: >98.0%(GC)

Color and Shape: Colorless to Light orange to Yellow clear liquid

Molecular weight: 129.20

Ref: 3B-P0348

1-(2-Hydroxyethyl)piperidine, 99%

CAS: 3040-44-6

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₇H₁₅NO

Purity: 99%

Color and Shape: Clear colorless to yellow to orange to brown, Viscous liquid

Molecular weight: 129.20

Ref: 02-B23816

2-(Piperidin-1-yl)ethanol

CAS: 3040-44-6

Formula: C₇H₁₅NO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 129.2001

Ref: IN-DA00300W

1-Piperidineethanol

CAS: 3040-44-6

Formula: C₇H₁₅NO

Purity: ≥ 99.0%

Color and Shape: Clear, colourless to light yellow liquid

Molecular weight: 129.20

Ref: 7W-GC6333

Raloxifene Impurity 13

CAS: 3040-44-6

Formula: C₇H₁₅NO

Color and Shape: Colorless Liquid

Molecular weight: 129.20

Ref: 4Z-R-0127

2-(Piperidin-1-yl)ethanol

CAS: 3040-44-6

2-(Piperidin-1-yl)ethanol

Purity: 99%

Molecular weight: 129.20g/mol

Ref: 54-OR95374

N-Piperidinoethanol

CAS: 3040-44-6

N-Piperidinoethanol is a biochemical.

Formula: C₇H₁₅NO

Color and Shape: Liquid

Molecular weight: 129.2

Ref: TM-T33732

1-Piperidineethanol

Controlled Product

CAS: 3040-44-6

Applications 1-Piperidineethanol (cas# 3040-44-6) is a compound useful in organic synthesis.

Formula: C₇H₁₅NO

Color and Shape: Neat

Molecular weight: 129.2

Ref: TR-P481950

2-(Piperidin-1-yl)ethanol

CAS: 3040-44-6

Formula: C₇H₁₅NO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 129.203

Ref: 10-F237773

Raloxifene Impurity 13

CAS: 3040-44-6

Formula: C₇H₁₅NO

Molecular weight: 129.20

Ref: ST-EA-CP-R2004

1-Piperidineethanol

CAS: 3040-44-6

1-Piperidineethanol is an active analogue of 1-piperidinepropanol. It has been shown to be a 5-HT4 receptor agonist that can inhibit the enzyme matrix polymerase, which is involved in the production of brain infarctions. The reaction mechanism for 1-piperidineethanol is not well understood, but it has been shown to react with hydrogen ions and amines to form a ternary complex. This complex reacts with hydrogen bond donors such as water or alcohols to form a reaction rate. The reaction rate depends on the concentration of hydrogen ions and amines in the solution.

Formula: C₇H₁₅NO

Purity: Min. 99%

Color and Shape: Colorless Clear Liquid

Molecular weight: 129.2 g/mol

Ref: 3D-FP16835