Epoxy curing agent Knowledge Pentamethylene 1,5-Pentamethylene-1H-tetrazole

Pentamethylene 1,5-Pentamethylene-1H-tetrazole

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Pentylenetetrazole Structural Formula

Structural formula

Business number 016N
Molecular formula C6H10N4
Molecular weight 138.17
label

1,5-pentamethylenetetrazole,

α,β-Cyclopentamethylenetetrazole,

1,5-Pentamethylenetetrazole,

6,7,8,9-Tetrahydro-5H-tetrazolo[1,5-a]azepine,

Metrazole,

Pentylenetetrazole

Numbering system

CAS number:54-95-5

MDL number:MFCD00005939

EINECS number:200-219-3

RTECS number:XF8225000

BRN number:135492

PubChem number:24278643

Physical property data

1. Character:White crystal. Odorless. Slightly spicy and bitter taste. Sexually stable.


2. Density (g/mL,25/4): Undetermined


3. Relative vapor density (g/mL,AIR=1): Undetermined


4. Melting point (ºC): 57~60


5. Boiling point (ºC,Normal pressure): Undetermined


6. Boiling point (ºC, 1.60kPa): 194


7. Refractive index: undetermined


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation (º): Undetermined


10. Autoignition point or ignition temperature (ºC): Undetermined


11. Vapor pressure (kPa,25ºC)�amily: Arial”>2. Molar Volume (m3/mol): 96.8


3. isotonic specific volume (90.2K):269.8


4. Surface Tension (dyne/cm):60.2


5. Polarizability10-24cm3):15.14

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 3

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: none

6. Topological molecule polar surface area 43.6

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 116

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

None

Storage method

This product should be sealed and stored away from light.

Synthesis method

Prepared by reacting cyclohexanone and hydrazoic acid

Purpose

cardiotonic. Biochemical research.
can be used for acute infectious diseases, anesthetics and Respiratory depression and acute circulatory failure caused by biturin poisoning. It can be used as a central stimulant (for human or veterinary use ). Preparations include injections.

>Prepared by reacting cyclohexanone and hydrazoic acid

Purpose

cardiotonic. Biochemical research.
can be used for acute infectious diseases, anesthetics and Respiratory depression and acute circulatory failure caused by biturin poisoning. It can be used as a central stimulant (for human or veterinary use ). Preparations include injections.

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