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2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1035373-85-3 Structure
  • Basic information

    1. Product Name: 2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride
    2. Synonyms: 2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride
    3. CAS NO:1035373-85-3
    4. Molecular Formula:
    5. Molecular Weight: 260.204
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1035373-85-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride(1035373-85-3)
    11. EPA Substance Registry System: 2-[2-(6-chloro-hexyloxy)ethoxy]ethylammonium hydrochloride(1035373-85-3)
  • 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: 1035373-85-3(Hazardous Substances Data)

1035373-85-3 Usage

Type of compound

Ammonium salt

Anion present

Hydrochloride (Cl-)

Type of cation

Quaternary ammonium (R4N+)

Alkyl chain length

Long (12 carbon atoms)

Functional groups

Hydroxy-ether (-OCH3) and ethoxy (-OCH2CH2)

Industrial and research applications

Surfactant, detergent, catalyst

Antimicrobial and antiseptic properties

Cationic nature

Potential use

Pharmaceuticals and disinfectants

Check Digit Verification of cas no

The CAS Registry Mumber 1035373-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,3,7 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1035373-85:
(9*1)+(8*0)+(7*3)+(6*5)+(5*3)+(4*7)+(3*3)+(2*8)+(1*5)=133
133 % 10 = 3
So 1035373-85-3 is a valid CAS Registry Number.

1035373-85-3Relevant articles and documents

BODIPY protein misfolding probe Hal-BODIPY, preparation method and application thereof

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, (2021/01/29)

The invention discloses a BODIPY protein misfolding probe Halo-BODIPY, a preparation method and application thereof, wherein the structural formula of the fluorescent probe is shown as a formula I inthe specification. According to the invention, the micro

FLUORESCENCE DYE

-

, (2020/07/07)

The present invention relates to compound according to formulas (1), (15), (16) or (17), the use of the compounds as a fluorescent dye, and a fluorescent dye comprising the compounds. The invention also relates to a method for fluorescence-based identific

DYES FOR ANALYSIS OF SOLUBLE PROTEIN AGGREGATES OR MISFOLDED PROTEIN OLIGOMERS

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Paragraph 0099; 00103, (2019/10/01)

Dye and compositions to monitor the multistep protein aggregation process in both test tubes and live cells are provided. These dyes can detect misfolded protein oligomers and distinguish insoluble protein aggregates from misfolded oligomers. Applications of these dyes include measuring kinetics of protein aggregation, monitoring aggregation of specific proteins in intact live cells, monitoring aggregation of cellular proteome in intact live cells, and tracking the time course of protein aggregation in cells under stress conditions.

Orientation-controlled conjugation of haloalkane dehalogenase fused homing peptides to multifunctional nanoparticles for the specific recognition of cancer cells

Mazzucchelli, Serena,Colombo, Miriam,Verderio, Paolo,Rozek, Ewa,Andreata, Francesco,Galbiati, Elisabetta,Tortora, Paolo,Corsi, Fabio,Prosperi, Davide

supporting information, p. 3121 - 3125 (2013/04/10)

In control: The ligand positioning and orientation on multifunctional nanoparticles (MNP) are controlled by using a versatile bimodular approach that exploits an 11 amino acid (U11) homing peptide genetically fused with a haloalkane dehalogenase (HALO) enzyme. The resultant nanoparticles have good targeting efficiency and selectivity toward broadly occurring urokinase plasminogen activator receptor positive human cancer cells.

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