69978-48-9

• 

• Basic information

  1. Product Name: 1,4,7,10-Tetraoxa-13-azacyclopentadecane, 13-butyl-
  2. Synonyms:
  3. CAS NO:69978-48-9
  4. Molecular Formula: C14H29NO4
  5. Molecular Weight: 275.389
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 69978-48-9.mol
  9. Article Data: 1

• 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: 1,4,7,10-Tetraoxa-13-azacyclopentadecane, 13-butyl-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 1,4,7,10-Tetraoxa-13-azacyclopentadecane, 13-butyl-(69978-48-9)
  11. EPA Substance Registry System: 1,4,7,10-Tetraoxa-13-azacyclopentadecane, 13-butyl-(69978-48-9)

• 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: 69978-48-9(Hazardous Substances Data)

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• SDS
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• 1,4,7,10-Tetraoxa-13-azacyclopentadecane, 13-butyl-

  Cas No: 69978-48-9

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• 10000 Metric Ton/Month

• Henan Wentao Chemical Product Co., Ltd.
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69978-48-9 Usage

Explanation

The compound has a ring structure, which is a common feature in organic chemistry. It is formed by the bonding of atoms in a closed loop.
3. Four oxygen atoms

Explanation

The compound contains four oxygen atoms that are part of the ring structure.
4. One nitrogen atom

Explanation

The compound has one nitrogen atom, which is also part of the ring structure.
5. Butyl group attachment

Explanation

A butyl group (a four-carbon chain) is attached to the 13th carbon atom in the cyclopentadecane ring.
6. Industrial applications

Explanation

The compound is used in various industrial processes, including the synthesis of complex organic molecules and the formulation of pharmaceuticals and agrochemicals.
7. Research purposes

Explanation

Due to its unique structure and properties, the compound is also utilized in scientific research for the development of new materials and applications.
8. Potential uses in materials science

Explanation

The compound's unique structure may offer opportunities for its use in the development of new materials with specific properties, such as improved strength, flexibility, or chemical resistance.
9. Pharmaceutical applications

Explanation

The compound may be used as a component in the formulation of certain pharmaceuticals, potentially contributing to the development of new drugs or therapies.
10. Agrochemical applications

Explanation

The compound may also be used in the development of agrochemicals, such as pesticides or fertilizers, to improve crop yield and protect plants from pests and diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 69978-48-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,9,7 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69978-48:
(7*6)+(6*9)+(5*9)+(4*7)+(3*8)+(2*4)+(1*8)=209
209 % 10 = 9
So 69978-48-9 is a valid CAS Registry Number.

69978-48-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	13-butyl-1,4,7,10-tetraoxa-13-azacyclopentadecane

1.2 Other means of identification

Product number	-
Other names	N-(n-butyl)monoza-15-crown-5

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:69978-48-9 SDS

69978-48-9Upstream product

• 102-79-4 n-butyldiethanolamine 
• 19249-03-7 triethylene glycol di-(p-toluenesulfonate) 

69978-48-9Downstream Products

69978-48-9Relevant articles and documents

LARIAT ETHERS. 3. MACROCYCLIC POLYETHERS BEARING DONOR GROUPS ON FLEXIBLE ARMS ATTACHED AT A NITROGEN PIVOT POINT

Schultz, Rose Ann,Dishong, Dennis M.,Gokel, George W.

, p. 2623 - 2626 (1981)

The binding of lariat ethers utilizing a nitrogen pivot atom for the donor sidearm is enhanced considerably relative to the carbon-based systems and this may be explicable in terms of diminished "sidedness."

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