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1,1-bis(4-methylphenyl)-3-(piperidin-1-yl)propan-1-ol hydrochloride (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39928-63-7

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39928-63-7 Usage

Chemical structure

A complex organic compound with a hydrochloride salt formed by the reaction of 1,1-bis(4-methylphenyl)-3-(piperidin-1-yl)propan-1-ol with hydrochloric acid.

Appearance

A solid substance, likely in the form of crystals or powder.

Solubility

Soluble in water and some organic solvents, such as ethanol and methanol.

Stability

Stable under normal temperature and pressure conditions, but sensitive to heat, light, and moisture.

Reactivity

Reacts with strong bases to form the free base form of the compound.

Primary use

As an intermediate in the synthesis of pharmaceutical drugs.

Potential applications

Development of antidepressant and antipsychotic medications due to its interaction with neurotransmitter receptors in the brain.

Additional uses

Treatment of various psychiatric and neurological disorders.

Research status

Further research and testing are necessary to fully understand its potential benefits and risks.

Safety precautions

Handle with care, as it may have potential side effects and should be used under the guidance of a healthcare professional.

Storage

Store in a cool, dry, and well-ventilated area, away from heat, light, and moisture.

Regulatory status

The compound may be subject to regulatory controls depending on the jurisdiction and its intended use in the pharmaceutical industry.

Environmental impact

The environmental impact of the compound is not well-established, but proper disposal and handling procedures should be followed to minimize potential harm.

Synthesis

The compound is synthesized through the reaction of 1,1-bis(4-methylphenyl)-3-(piperidin-1-yl)propan-1-ol with hydrochloric acid.

Check Digit Verification of cas no

The CAS Registry Mumber 39928-63-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,2 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39928-63:
(7*3)+(6*9)+(5*9)+(4*2)+(3*8)+(2*6)+(1*3)=167
167 % 10 = 7
So 39928-63-7 is a valid CAS Registry Number.

39928-63-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-bis(4-methylphenyl)-3-piperidin-1-ylpropan-1-ol,hydrochloride

1.2 Other means of identification

Product number -
Other names 1,1-bis(4-methylphenyl)-3-(piperidin-1-yl)propan-1-ol hydrochloride(1:1)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:39928-63-7 SDS

39928-63-7Upstream product

39928-63-7Downstream Products

39928-63-7Relevant academic research and scientific papers

Synthesis and pharmacology of basic sec, tert alcohols and derivatives (Japanese)

Igarashi,Kurihara

, p. 554 - 565 (2007/10/05)

In order to investigate the relation between chemical structure and pharmacological properties, 68 new compounds belonging to amino alcohol derivatives were synthesized. One of them showed twice as potent an analgesic activity as barbipyrine, and five of them were found to be as effective as barbipyrine. Antispasmodic activity was recognized in the solution of these compounds at the concentration from 10-4 to 10-7 g/ml. Almost all the compounds were shown to have local anesthetic activity and the duration of the activity of several substances was more than 120 min. In general, the pharmacological activity decreased in the order of aminoolefins, urethans, amino alcohols, and alkamine esters.

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