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2-(2,5-diaminophenoxy)ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 126335-43-1 Structure
  • Basic information

    1. Product Name: 2-(2,5-diaminophenoxy)ethanol
    2. Synonyms:
    3. CAS NO:126335-43-1
    4. Molecular Formula: C8H12N2O2
    5. Molecular Weight: 168.1931
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 126335-43-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 393.3°C at 760 mmHg
    3. Flash Point: 191.7°C
    4. Appearance: N/A
    5. Density: 1.274g/cm3
    6. Vapor Pressure: 6.83E-07mmHg at 25°C
    7. Refractive Index: 1.64
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(2,5-diaminophenoxy)ethanol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(2,5-diaminophenoxy)ethanol(126335-43-1)
    12. EPA Substance Registry System: 2-(2,5-diaminophenoxy)ethanol(126335-43-1)
  • 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: 126335-43-1(Hazardous Substances Data)

126335-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 126335-43-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,3 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 126335-43:
(8*1)+(7*2)+(6*6)+(5*3)+(4*3)+(3*5)+(2*4)+(1*3)=111
111 % 10 = 1
So 126335-43-1 is a valid CAS Registry Number.

126335-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-diaminophenoxy)ethanol

1.2 Other means of identification

Product number -
Other names -

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:126335-43-1 SDS

126335-43-1Upstream product

126335-43-1Downstream Products

126335-43-1Relevant articles and documents

1,3-Dihydroxybenzene derivatives and colorants containing said compounds

-

, (2008/06/13)

1,3-Dihydroxybenzene derivatives of general formula (I) or (Ia) or physiologically tolerated, water-soluble thereof wherein R′1 denotes substituted pyridyl group, a pyrimidyl group, a group of formula (IIa) or (IIIa) and the dyeing agents for keratin fibers containing these compounds.

Means and method for dying keratinic fibers

-

, (2008/06/13)

Composition for coloring keratin fibers based on a developer-coupler combination characterized in that it contains as the coupler 3-(2,4-diaminophenoxy)-1-propanol and as the developer a p-phenylenediamine derivative monosubstituted on the benzene ring and having general formula (I) ?and/or a 4,5-diamino-1H-pyrazole derivative of general formula (II) ?and/or a p-aminophenol derivative of general formula (III) ?as well as a method for the oxidative coloring of hair, and the use of said composition.

1,4-diazacycloheptane derivatives and their use in hair oxidation dyes

-

, (2008/06/13)

A 1,4-diazacycloheptane derivative and an oxidative hair colorant containing the derivative as a primary intermediate is presented. The 1,4-diazacycloheptane derivative is of the formula: STR1 where R1, R2, R3 and R4 independently of one another represent hydrogen, a C1-4 alkyl or hydroxyalkyl group or a C2-4, dihydroxyalkyl group, X and Y independently of one another represent hydrogen, chlorine, fluorine, a C1-4 alkyl, hydroxyalkyl, aminoakyl or alkoxy group, a C2-4 dihydroxyalkyl group or an allyl group and R5 and R6 independently of one another represent hydrogen or a C1-4 alkyl group. Natural color tones can be obtained in keratin fibers with oxidative hair colorants containing the 1,4-diazacycloheptane derivative, without the use of additional primary intermediates.

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