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3-Isobutylamino-propan-1-ol, also known as ibutolol, is a chemical compound that functions as a beta-adrenergic blocking agent. It is known for its effects on the heart and circulation, playing a crucial role in the management of cardiovascular conditions.
Used in Pharmaceutical Industry:
3-Isobutylamino-propan-1-ol is used as a therapeutic agent for the treatment of high blood pressure and heart failure. It operates by relaxing blood vessels and slowing the heart rate, which enhances blood flow and reduces blood pressure. 3-ISOBUTYLAMINO-PROPAN-1-OL is typically incorporated into medication formulations and should be administered under the guidance of a healthcare professional to ensure safe and effective use, adhering to prescribed dosage and treatment protocols.

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  • 285124-45-0 Structure
  • Basic information

    1. Product Name: 3-ISOBUTYLAMINO-PROPAN-1-OL
    2. Synonyms: 3-ISOBUTYLAMINO-PROPAN-1-OL;3-[(2-methylpropyl)amino]-1-Propanol
    3. CAS NO:285124-45-0
    4. Molecular Formula: C7H17NO
    5. Molecular Weight: 131.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 285124-45-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 202.5°Cat760mmHg
    3. Flash Point: 64.4°C
    4. Appearance: /
    5. Density: g/cm3
    6. Vapor Pressure: 0.0712mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 15.04±0.10(Predicted)
    11. CAS DataBase Reference: 3-ISOBUTYLAMINO-PROPAN-1-OL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 3-ISOBUTYLAMINO-PROPAN-1-OL(285124-45-0)
    13. EPA Substance Registry System: 3-ISOBUTYLAMINO-PROPAN-1-OL(285124-45-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 285124-45-0(Hazardous Substances Data)

285124-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 285124-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,5,1,2 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 285124-45:
(8*2)+(7*8)+(6*5)+(5*1)+(4*2)+(3*4)+(2*4)+(1*5)=140
140 % 10 = 0
So 285124-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H17NO/c1-7(2)6-8-4-3-5-9/h7-9H,3-6H2,1-2H3/p+1

285124-45-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-methylpropylamino)propan-1-ol

1.2 Other means of identification

Product number -
Other names BB_SC-1146

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:285124-45-0 SDS

285124-45-0Downstream Products

285124-45-0Relevant articles and documents

A practical synthesis of N-alkyl- and N,N′-dialkyl-polyamines This work is dedicated to the memory of our dear colleague and friend Mr. Charles Edward Price

Haussener, Travis J.,Sebahar, Paul R.,Kanna Reddy, Hariprasada R.,Williams, Dustin L.,Looper, Ryan E.

supporting information, p. 2845 - 2848 (2016/06/14)

A variety of polyamines have been synthesized from their corresponding amino alcohols through a 3-step process. The synthesis predicates that the most likely impurities are of higher molecular weight and that distillation is effective at producing highly pure materials. This sequence is scalable, requires no protecting groups or chromatography, and provides the requisite polyamines in moderate to good yields.

METHOD OF PRODUCING N-ALKYL POLYAMINES

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Page/Page column 20, (2016/03/22)

In one embodiment, the invention presents a process for the preparation of N-alkyl polyamines that includes (i) the conversion of an amino alcohol to an aminoalkyl alkylating agent with a halo or aldehyde reactive group and (ii) the addition of amines to an aminecontaining alkylating agent to make an N-alkyl polyamine.

Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents

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Page column 44, (2010/02/05)

This invention relates to 2-arylimino heterocycles, including 2-arylimino-1,3-thiazolidines, 2-arylimino-2,3,4,5-tetrahydro-1,3-thiazines, 2-arylimino-1,3-thiazolidin-4-ones, 2-arylimino-1,3-thiazolidin-5-ones, and 2-arylimino-1,3-oxazolidines, and their use in modulating progesterone receptor mediated processes, and pharmaceutical compositions for use in such therapies.

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