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CAS

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6927-73-7

P-butyloxyaniline hydrochloride, also known as 4-butoxyaniline hydrochloride, is a chemical compound with the molecular formula C10H16ClNO. It is a derivative of aniline, where a butoxy group (C4H9O) is attached to the para position of the benzene ring. P-BUTYLOXYANILINE HYDROCHLORIDE is a white to off-white crystalline solid and is soluble in water. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. P-butyloxyaniline hydrochloride is also known for its potential applications in the production of rubber chemicals and as a corrosion inhibitor. Due to its reactivity and potential health hazards, it is essential to handle P-BUTYLOXYANILINE HYDROCHLORIDE with proper safety measures and in accordance with relevant regulations.

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  • 6927-73-7 Structure

  • Basic information

    1. Product Name: P-BUTYLOXYANILINE HYDROCHLORIDE
    2. Synonyms: P-BUTYLOXYANILINE HYDROCHLORIDE
    3. CAS NO:6927-73-7
    4. Molecular Formula: C10H15NO*ClH
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6927-73-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 312.8°C at 760 mmHg
    3. Flash Point: 143°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 0.000382mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: P-BUTYLOXYANILINE HYDROCHLORIDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: P-BUTYLOXYANILINE HYDROCHLORIDE(6927-73-7)
    12. EPA Substance Registry System: P-BUTYLOXYANILINE HYDROCHLORIDE(6927-73-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 6927-73-7(Hazardous Substances Data)

6927-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6927-73-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6927-73:
(6*6)+(5*9)+(4*2)+(3*7)+(2*7)+(1*3)=127
127 % 10 = 7
So 6927-73-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO.ClH/c1-2-3-8-12-10-6-4-9(11)5-7-10;/h4-7H,2-3,8,11H2,1H3;1H

6927-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-butoxyaniline,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Butoxy-anilin,Hydrochlorid

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:6927-73-7 SDS

6927-73-7Relevant articles and documents

Comparative Structure-Activity Relationships of Antifolate Triazines Inhibiting Murine Tumor Cells Sensitive and Resistant to Methotrexate

Selassie, Cynthia Dias,Hansch, Corwin,Khwaja, Tasneem A.,Dias, Cecilia B.,Pentecost, Stephanie

, p. 347 - 357 (2007/10/02)

The inhibitory effect of 108 4,6-diamino-1,2-dihydro-2,2-dimethyl-1-(substituted-phenyl)-s-triazines on murine L5178Y tumor cells, resistant and sensitive to methotrexate (MTX), has been studied.From the pI50 values, quantitative structure-activity relationships have been formulated which show that the lipophilic triazines are much more inhibitory against resistant cells than methotrexate or hydrophilic triazines.The results are compared with the behavior of other antifolate drugs that have been used in chemotherapy, as well as with eight antitumor drugs that are notantifolates.The acquired resistance of these cells toward hydrophilic antifolates may be attributed to the combined effect of an impaired active-transport system, a change in the conformation of dihydrofolate reductase in the resistant cells, and an amplified production of dihydrofolate reductase in the resistant cells.

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