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22663-61-2

2-METHYL-1-DODECANOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22663-61-2 Structure

  • Basic information

    1. Product Name: 2-METHYL-1-DODECANOL
    2. Synonyms: 2-METHYL-1-DODECANOL
    3. CAS NO:22663-61-2
    4. Molecular Formula: C13H28O
    5. Molecular Weight: 200.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22663-61-2.mol

  • Chemical Properties

    1. Melting Point: 26.15°C (estimate)
    2. Boiling Point: 268.11°C (estimate)
    3. Flash Point: 105.5°C
    4. Appearance: /
    5. Density: 0.7947 (estimate)
    6. Vapor Pressure: 0.00173mmHg at 25°C
    7. Refractive Index: 1.4192 (estimate)
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 15.04±0.10(Predicted)
    11. CAS DataBase Reference: 2-METHYL-1-DODECANOL(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-METHYL-1-DODECANOL(22663-61-2)
    13. EPA Substance Registry System: 2-METHYL-1-DODECANOL(22663-61-2)

  • 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: 22663-61-2(Hazardous Substances Data)

22663-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22663-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,6,6 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 22663-61:
(7*2)+(6*2)+(5*6)+(4*6)+(3*3)+(2*6)+(1*1)=102
102 % 10 = 2
So 22663-61-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H28O/c1-3-4-5-6-7-8-9-10-11-13(2)12-14/h13-14H,3-12H2,1-2H3

22663-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-METHYL-1-DODECANOL

1.2 Other means of identification

Product number -
Other names methyl-2 dodecanol-1

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:22663-61-2 SDS

22663-61-2Relevant articles and documents

From alkenes to alcohols by cobalt-catalyzed hydroformylation-reduction

Achonduh, George,Yang, Qian,Alper, Howard

supporting information, p. 1241 - 1246 (2015/03/05)

The cobalt-catalyzed hydroformylation of alkenes in the presence of a range of novel cyclic phosphine ligands was investigated. The effect of various parameters such as solvents, additives, cobalt/phosphine ratio, CO/H2 (1:2), and nature of the alkenes was examined. The results revealed that both terminal and internal alkenes are hydroformylated in high yields to give mainly linear products at moderate temperature and syn gas pressure. The linearity ranges from 43 to 85%, with Lim-10 giving the highest proportion of linear product.

From olefins to alcohols: Efficient and regioselective ruthenium-catalyzed domino hydroformylation/reduction sequence

Fleischer, Ivana,Dyballa, Katrin Marie,Jennerjahn, Reiko,Jackstell, Ralf,Franke, Robert,Spannenberg, Anke,Beller, Matthias

supporting information, p. 2949 - 2953 (2013/04/10)

Exploring the alternatives: Ruthenium imidazoyl phosphine complexes catalyze the domino hydroformylation/reduction of alkenes to alcohols in good yields and with good selectivities (see scheme). Linear aliphatic alcohols are synthesized under reaction conditions typically used in industrial hydroformylations. Copyright

Formic acid: A promising bio-renewable feedstock for fine chemicals

Mura, Manuel G.,Luca, Lidia De,Giacomelli, Giampaolo,Porcheddu, Andrea

supporting information, p. 3180 - 3186 (2013/01/15)

In light of the growing scarcity of petroleum-based raw materials, carbon dioxide (CO2) is becoming increasing attractive as organic carbon source. In this perspective, formic acid (HCOOH) might be an interesting bio-renewable solution to store, transport, and activate carbon dioxide for the synthesis of value-added chemicals. Herein, HCOOH has been successfully used as C1 building block for the synthesis of a library of alcohols via a catalysed oxo-synthesis, under green experimental conditions. Copyright

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