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16-CARBOXYHEXADECYL DISULFIDE, 99% is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112122-99-3 Structure
  • Basic information

    1. Product Name: 16-CARBOXYHEXADECYL DISULFIDE, 99%
    2. Synonyms: 16-CARBOXYHEXADECYL DISULFIDE, 99%;16,16′-Dithiobis-hexadecanoic acid
    3. CAS NO:112122-99-3
    4. Molecular Formula: C32H62O4S2
    5. Molecular Weight: 603.01544
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112122-99-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 16-CARBOXYHEXADECYL DISULFIDE, 99%(CAS DataBase Reference)
    10. NIST Chemistry Reference: 16-CARBOXYHEXADECYL DISULFIDE, 99%(112122-99-3)
    11. EPA Substance Registry System: 16-CARBOXYHEXADECYL DISULFIDE, 99%(112122-99-3)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112122-99-3(Hazardous Substances Data)

112122-99-3 Usage

Purity level

99%

Type of compound

Disulfide compound

Functional groups

Carboxyl group and hexadecyl chain

Industrial applications

Building block in the synthesis of other organic compounds

Research applications

Reagent in chemical reactions

Material science

Crosslinking agent

Nanotechnology

Surface modifier

Suitability

Sensitive research and manufacturing processes

Advantage

Precise control over chemical composition due to high purity level

Check Digit Verification of cas no

The CAS Registry Mumber 112122-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,2 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112122-99:
(8*1)+(7*1)+(6*2)+(5*1)+(4*2)+(3*2)+(2*9)+(1*9)=73
73 % 10 = 3
So 112122-99-3 is a valid CAS Registry Number.

112122-99-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Aldrich

  • (674443)  16-Carboxyhexadecyldisulfide  97%

  • 112122-99-3

  • 674443-250MG

  • 3,601.26CNY

  • Detail

112122-99-3SDS

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 17-(16-carboxyhexadecyldisulfanyl)heptadecanoic acid

1.2 Other means of identification

Product number -
Other names Hexadecanoic acid,16,16'-dithiobis

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:112122-99-3 SDS

112122-99-3Downstream Products

112122-99-3Relevant articles and documents

Functionalized surface arrays for spatial targeting of immune cell signaling

Senaratne, Wageesha,Sengupta, Prabuddha,Jakubek, Vladimir,Holowka, David,Ober, Christopher K.,Baird, Barbara

, p. 5594 - 5595 (2006)

The effect of surface topography and chemistry on cellular response is of fundamental importance, especially where living systems encounter device surfaces as in medical implants, tissue engineering, and cell-based sensors. To understand these biological

Photoinduced polymerization from dimethylamino-terminated self-assembled monolayers on gold

Dyer, Daniel J.,Feng, Jianxin,Schmidt, Rolf,Wong, Ven Ney,Zhao, Tongfeng,Yagci, Yusuf

, p. 7072 - 7074 (2007/10/03)

Dimethylamino-terminated self-assembled monolayers (SAM) were used to perform photoinduced polymerization on gold. The photochemical initiation was more rapid than thermal and allowed the lithographic patterning of planar substrates. It was found that dia

Model systems for molecular recognition at interfaces: Synthesis and characterisation of functionalised disulfides with hydrogen-bonding properties

Steinbeck, Martin,Ringsdorf, Helmut

, p. 1193 - 1194 (2007/10/03)

A series of symmetrical alkane disulfides bearing derivatives of barbituric acid and 2,4,5,6-tetraaminopyrimidine, respectively, as headgroups are synthesised, which can be used for the preparation of functionalised monolayers on gold.

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