Epoxy curing agent Knowledge Tris(hydroxymethyl)nitromethane Tris(hydroxymethyl)nitromethane

Tris(hydroxymethyl)nitromethane Tris(hydroxymethyl)nitromethane

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Tris(hydroxymethyl)nitromethane structural formula

Structural formula

Business number 03JX
Molecular formula C4H9NO5
Molecular weight 151.12
label

2-Hydroxymethyl-2-nitro-1,3-propanediol,

aliphatic compounds

Numbering system

CAS number:126-11-4

MDL number:MFCD00007395

EINECS number:204-769-5

RTECS number:TY7350000

BRN number:1768985

PubChem number:24846654

Physical property data

1.Character: white crystal


2. Melting point: 214℃


3. Solubility: 220g/100ml (in 20℃ water)


4. Solubility: Easily soluble in alcohol, slightly soluble in benzene and other hydrocarbons


5. Acidity and alkalinity: the pH of 0.1M aqueous solution is 4.5

Toxicological data

Acute toxicity data


Rat oral LD50: 1900mg/kg


Mouse oral LD50: 1900mg/kg


Mouse abdominal cavity LD50: 4mg/kg


Rabbit oral administrationLDLo: 250 mg/kg

Ecological data

None

Molecular structure data

5. Molecular property data:


1 , Molar refractive index:31.17


2. Molar volume (m3/mol):99.9


3. isotonic specific volume (90.2K):295.1


4. Surface Tension (dyne/cm):76.1


5. Polarizability10-24cm3):12.35

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -2.2

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 5

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: none

6. Topological molecule polar surface area 107

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 107

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

Basic properties: Easily decomposes at high temperatures and has no boiling point

Storage method

Storage: Store sealed in a cool and ventilated place.

Synthesis method

Brief description of production method: Obtained from the condensation of nitromethane and formaldehyde under alkaline conditions. Raw material consumption (kg/t) nitromethane (≥95%) 634, formaldehyde (≥30%) 2120

Purpose

Purpose: Disinfectant for inanimate objects. Used in circulating industrial water systems, cutting oils, non-protein glues and slurries to inhibit bacterial growth. Drug buffer acid amine intermediate.

�: Store sealed in a cool and ventilated place.

Synthesis method

Brief description of production method: Obtained from the condensation of nitromethane and formaldehyde under alkaline conditions. Raw material consumption (kg/t) nitromethane (≥95%) 634, formaldehyde (≥30%) 2120

Purpose

Purpose: Disinfectant for inanimate objects. Used in circulating industrial water systems, cutting oils, non-protein glues and slurries to inhibit bacterial growth. Drug buffer acid amine intermediate.

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