Epoxy curing agent Knowledge m-Nitrotoluene m-Nitrotoluene

m-Nitrotoluene m-Nitrotoluene

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m-nitrotoluene structural formula

Structural formula

Business number 02F6
Molecular formula C7H7NO2
Molecular weight 137
label

3-nitrotoluene,

1-Methyl-3-nitrobenzene,

m-methylnitrobenzene,

3-Nitrotoluene,

1-Methyl-3-mitrobenzene,

3-Methylnitrobenzene,

Pesticide intermediates; aromatic nitrogen-containing compounds and their derivatives

Numbering system

CAS number:99-08-1

MDL number:MFCD00007265

EINECS number:202-728-6

RTECS number:XT2975000

BRN number:1906910

PubChem number:24897588

Physical property data

1. Properties: yellow liquid or crystal[1]

2. Melting point (℃): 15.1[2]

3. Boiling point (℃): 231.9[3]

4. Relative density (water=1): 1.16[4]

5. Relative vapor density (air=1): 4.72[5]

6. Saturated vapor pressure (kPa): 0.13 (50.2℃)[6]

7. Critical pressure (MPa): 3.8[7]

8. Octanol/water partition coefficient :2.4~2.45[8]

9. Flash point (℃): 101.67[9]

10. Ignition temperature (℃): 305[10]

11. Explosion upper limit (%): No data available

12. Explosion lower limit (%): 1.6[11]

13. Solubility: insoluble in water, soluble in benzene, miscible in ethanol and ether. [12]

Toxicological data

1. Acute toxicity[13]

LD50: 1072mg/kg (rat oral)

LC50 : 693mg/m3 (rat inhalation)

2. Irritation No information available

Ecological data

1. Ecotoxicity[14]

LC50: 33.14mg/L (96h) (zebrafish); 71mg/L (48h) ) (Medaka); 7.5mg/L (48h) (Daphnia)

EC50: 14mg/L (96h) (Single-cell green algae)

2. Biodegradability [15] MITI-I test, initial concentration 100ppm, sludge concentration 30ppm, 2% degradation after 14 days.

3. Non-biodegradability No information available

Molecular structure data

1. Molar refractive index: 37.62

2. Molar volume (cm3/mol): 117.5

3. Isotonic specific volume (90.2K ): 300.4

4. Surface tension (dyne/cm): 42.6

5. Dielectric constant:

6. Dipole moment (10-24cm3):

7. Polarizability: 14.91

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): 2.4

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers:

6. Topological molecular extremes��Surface area (TPSA): 43.1

7. Number of heavy atoms: 10

8. Surface charge: 0

9. Complexity: 130

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10. Number of isotope atoms: 0

11. Number of determined atomic stereocenters: 0

12. Number of uncertain atomic stereocenters: 0

13. The number of determined stereocenters of chemical bonds: 0

14. The number of uncertain stereocenters of chemical bonds: 0

15. The number of covalent bond units: 1

Properties and stability

1. Stability[16] Stable

2. Incompatible substances[17] Strong oxidizing agent, strong reducing agent, strong alkali

3. Conditions to avoid contact[18] Heating

4. Polymerization hazard[19] No polymerization

5. Decomposition products[20] Nitrogen oxides

Storage method

Storage Precautions[21] Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature does not exceed 35°C and the relative humidity does not exceed 80%. The packaging is sealed. They should be stored separately from oxidants, reducing agents, alkalis, and food chemicals, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills.

Synthesis method

In the industrial production of o-nitrotoluene and p-nitrotoluene, m-nitrotoluene can be recovered at the same time. m-nitrotoluene can be prepared from 3-nitro-4-aminotoluene through the following process, with a yield of about 67%.

Purpose

1. Used to prepare naphthol AS-BS and m-nitrobenzoic acid. It is also used in pesticides, medicines, color developers, plastic and synthetic fiber additives, etc.

2. Used in organic synthesis. [22]

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