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Fluorescent Brightener 135 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1041-00-5 Structure
  • Basic information

    1. Product Name: Fluorescent Brightener 135
    2. Synonyms: 1,2-bis(5-methyl-2-benzoxazole)ethylene;2,2'-(1,2-ethenediyl)bis[5-methylbenzoxazole];C.I. 481520;fluorescent brightener 135;2,2'-vinylenebis[5-methylbenzoxazole];Fluorescent Whitener DT;1.2 DI(5-MYTHYL-BENZIAZOLYL)ETHYLENE;Fluorescent brightener 135,2,2'-(1,2-Ethenediyl)bis[5-methylbenzoxazole]
    3. CAS NO:1041-00-5
    4. Molecular Formula: C18H14N2O2
    5. Molecular Weight: 290.32
    6. EINECS: 213-866-1
    7. Product Categories: N/A
    8. Mol File: 1041-00-5.mol
  • Chemical Properties

    1. Melting Point: 180-181°C
    2. Boiling Point: 471.197 °C at 760 mmHg
    3. Flash Point: 237.309 °C
    4. Appearance: /
    5. Density: 1.287
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.87±0.10(Predicted)
    10. Water Solubility: 290μg/L at 20℃
    11. CAS DataBase Reference: Fluorescent Brightener 135(CAS DataBase Reference)
    12. NIST Chemistry Reference: Fluorescent Brightener 135(1041-00-5)
    13. EPA Substance Registry System: Fluorescent Brightener 135(1041-00-5)
  • 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: 1041-00-5(Hazardous Substances Data)

1041-00-5 Usage

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 1041-00-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1041-00:
(6*1)+(5*0)+(4*4)+(3*1)+(2*0)+(1*0)=25
25 % 10 = 5
So 1041-00-5 is a valid CAS Registry Number.

1041-00-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Fluorescent Brightener 135

1.2 Other means of identification

Product number -
Other names 1.2 DI(5-MYTHYL-BENZIAZOLYL)ETHYLENE

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:1041-00-5 SDS

1041-00-5Downstream Products

1041-00-5Relevant articles and documents

Photoactivatable turn-on fluorescence based on the photo-cleavage of the C-Br bond in 1,2-bis(5-(bromoethyl)benzoxazol-2-yl)ethane

Hao, Yongchao,Dong, Xian-Zi,Chen, Yi

, p. 3468 - 3472 (2014)

This paper describes photoactivatable turn-on fluorescence based on the photo-cleavage of the C-Br bond in 1,2-bis(5-(bromoethyl)benzoxazol-2-yl)ethane (1) in both solution and in a polymeric thin film. It was found that 1 exhibited very weak fluorescence in both solution and in a PMMA thin film, upon irradiation with 365 nm light, a strong fluorescence was detected. The strong fluorescence attributed to the photo-product resulted from the photo-induced cleavage of the C-Br bond in 1. Moreover, it was also found that the photo-cleavage of the C-Br bond in 1 can be performed using a two-photon induced process, and upon irradiation on a 1-PMMA thin film with a 780 nm femtosecond laser, finely resolved fluorescence images are obtained.

Method For Producing Bisbenzoxazoles

-

Page/Page column 6, (2010/04/23)

The invention relates to a method for producing bisbenzoxazoles that are interconnected by means of a system of conjugated double bonds, according to which o-aminophenols are reacted with dicarboxylic acids, the carboxyl groups of which are interconnected via a double bond or a system of conjugated double bonds, to form an ammonium salt, said ammonium salt being converted in the presence of dehydrogenating catalysts and solvents with a low dielectric loss into benzoxazol by means of microwave radiation.

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