1577-43-1

• 

• Basic information

  1. Product Name: 1-Acetoxynonadecane
  2. Synonyms: 1-Acetoxynonadecane
  3. CAS NO:1577-43-1
  4. Molecular Formula: C21H42 O2
  5. Molecular Weight: 326.56
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1577-43-1.mol
  9. Article Data: 3

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 354.3±5.0 °C(Predicted)
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: 0.862±0.06 g/cm3(Predicted)
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 1-Acetoxynonadecane(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1-Acetoxynonadecane(1577-43-1)
  11. EPA Substance Registry System: 1-Acetoxynonadecane(1577-43-1)

• 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: 1577-43-1(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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1577-43-1 Usage

Type of compound

Long-chain carboxylic acid derivative

Backbone

Nonadecane

Attached group

Acetate group

Attachment position

First carbon

Applications

Research and industrial applications

Use as a precursor

Synthesis of other organic compounds

Biological activities

Antimicrobial and antifungal properties

Potential use

Pharmaceuticals

Role in production

Building block for various chemical products

Check Digit Verification of cas no

The CAS Registry Mumber 1577-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,7 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1577-43:
(6*1)+(5*5)+(4*7)+(3*7)+(2*4)+(1*3)=91
91 % 10 = 1
So 1577-43-1 is a valid CAS Registry Number.

InChI:InChI=1S/C21H42O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23-21(2)22/h3-20H2,1-2H3

1577-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	nonadecyl acetate

1.2 Other means of identification

Product number	-
Other names	1-Nonadecanol,acetate (7CI,8CI,9CI)

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:1577-43-1 SDS

1577-43-1Upstream product

• 1454-84-8 nonadecan-1-ol 
• 108-24-7 acetic anhydride 
• 64-19-7 acetic acid 
• 7206-25-9 trans-9-octadecene 
• 75-36-5 acetyl chloride 

1577-43-1Downstream Products

1577-43-1Relevant articles and documents

Solvent-free esterification of carboxylic acids and alcohols in the presence of silphos [PCl3-n(SiO2)n] as a heterogeneous phosphine reagent

Rao, Ambati Narasimha,Ganesan, Kumaran,Shinde, Chandra Kant

experimental part, p. 2299 - 2308 (2012/06/18)

An efficient solvent-free method for the preparation of esters from various aromatic and aliphatic acids with primary, secondary, and tertiary alcohols using a heterogeneous phosphine reagent, silphos [PCl3-n(SiO 2)n], in good yields is reported.

Reptilian chemistry: volatile compounds from paracloacal glands of the American crocodile (Crocodylus acutus).

Garcia-Rubio, Silvina,Attygalle, Athula B,Weldon, Paul J,Meinwald, Jerrold

, p. 769 - 781 (2007/10/03)

The secretion of the paracloacal glands of the American crocodile (Crocodylus acutus) contains over 80 lipophilic compounds, including saturated and unsaturated long-chain alcohols along with their formic, acetic, and butyric acid esters, and several isoprenoids. Most of these compounds were identified on the basis of mass spectra, obtained by GC-MS. In addition, identification of the major components was supported by infrared spectra obtained by GC-FTIR. Major differences are indicated in the composition of the paracloacal gland secretion of C. acutus and that of another crocodylid, the African dwarf crocodile (Osteolaemus tetraspis).

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