O-aminophenol

Ortho-aminophenol structural formula

Structural formula

Business number 029C
Molecular formula C6H7NO
Molecular weight 109
label

o-Hydroxyaniline,

2-Aminophenol,

1-amino-2-hydroxybenzene,

2-Amino-1-hydroxybenzene,

o-Aminophenol,

2-Aminophenol,

Aromatic nitrogen-containing compounds and their derivatives

Numbering system

CAS number:95-55-6

MDL number:MFCD00007690

EINECS number:202-431-1

RTECS number:SJ4950000

BRN number:606075

PubChem number:24891176

Physical property data

1. Properties: white or light gray crystalline powder. [1]

2. Melting point (?): 170~174[2]

3. Octanol/water Distribution coefficient: 0.52~0.62[3]

4. Solubility: soluble in cold water, ethanol, benzene, and ether. [4]

Toxicological data

1. Acute toxicity[5]

LD50: 951mg/kg (rat oral); 800mg/kg (mouse oral Oral); >1g/kg (guinea pig transdermal)

2. Irritation [6] Rabbit eye: 100mg, mild irritation .

3. Mutagenicity [7] Microbial mutagenicity: Salmonella typhimurium 333?g/dish.

4. Teratogenicity[8] The lowest toxic dose (TDLo) of 150mg/kg was given intraperitoneally to hamsters on the 8th day after pregnancy, causing damage to the central nervous system. , eyes, ears, and musculoskeletal system developmental malformations. DNA inhibition: hamster lung 19 ?mol/L.

Ecological data

1. Ecotoxicity No data yet

2. Biodegradability[9] When the COD value of 2-aminophenol is 200 mg/L, domesticated activated sludge is used, and the sludge concentration reaches 100 mg/L. After 5 days (aerobic), the COD removal rate is 95%.

3. Non-biodegradability[10] In the air, when the hydroxyl radical concentration is 5.00×105 pcs/cm3, the degradation half-life is 5h (theoretical).

Molecular structure data

1. Molar refractive index: 32.37

2. Molar volume (cm3/mol): 90.1

3. Isotonic specific volume (90.2K ): 248.1

4. Surface tension (dyne/cm): 57.4

5. Polarizability (10-24cm3): 12.83

Compute chemical data

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

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 0

5. Number of tautomers: 7

6. Topological molecule polar surface area 46.2

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 74.9

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determined number of chemical bond stereocenters: 0

14. Uncertain number of chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stability[11] Stable

2. Incompatible substances[12] Strong oxidants, acid chlorides, acid anhydrides, acids, chloroform

3. Conditions to avoid contact [13] Heat

>

4. Hazards of aggregation[14] No aggregation

Storage method

Storage Precautions[15] Store in a cool, ventilated warehouse. Keep away from fire and heat sources. The packaging is sealed. They should be stored separately from oxidants, acids, 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

Heat o-nitrochlorobenzene in a sodium hydroxide solution and hydrolyze it under a certain pressure to obtain sodium o-nitrophenolate, which is then reduced with alkali sulfide. Then use carbonic acid to separate, cool, filter, soak in sodium bisulfite solution, centrifuge, and dry to obtain the finished product.


Purpose

1. Dye intermediates, used to manufacture sulfur dyes, azo dyes, fur dyes and fluorescent whitening agent EB, etc. Raw materials used in the pesticide industry for the pesticide phosphos.

2. Mainly used to make acid medium blue R, sulfur yellow brown, etc., and can also be used as fur dye. Used in the cosmetics industry to make hair dyes (as compound dyes).

3. Determination of silver and tin and verification of gold. Intermediate of diazo dyes and sulfur dyes.

4. Used in the manufacture of dyes, drugs, and plastic curing agents. [16]

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Prednisolone acetate

Prednisolone acetate structural formula

Structural formula

Business number 015E
Molecular formula C23H30O6
Molecular weight 402.49
label

Prednisolone acetate,

prednisone acetate,

Dehydrohydrocortisone acetate,

11b,17a,21-Trihydroxypregnant-1,4-diene-3,20-dione-21-acetate,

Prednisolone acetate,

dehydrocortisol acetate,

Predsolone acetate,

dehydrocortisol acetate,

21-Acetoxy-1,4-pregnadiene-11?,17?-diol-3,20-dione,

Prednisolone 21-acetate,

11?,17?,21-Trihydroxy-1,4-pregnadiene-3,20-dione 21-acetate,

1,4-Pregnadiene-11?,17?,21-

Numbering system

CAS number:52-21-1

MDL number:MFCD00037710

EINECS number:200-134-1

RTECS number:TU4152500

BRN number:3111798

PubChem number:24898962

Physical property data

1. Properties: colorless crystalline powder. Odorless. Bitter taste.

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

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

4. Melting point (ºC): 237-239

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

6. Boiling point (ºC, 5.2kPa): Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): Undetermined Determined

10. Autoignition point or ignition temperature (ºC): Not determined

11. Vapor pressure (kPa, 25ºC): Not determined

12. Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit ( %, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Insoluble in water, soluble in ethanol, Slightly soluble in chloroform and acetone.

Toxicological data

1. Acute toxicity: rat subcutaneous LD50: >240mg/kg; mouse subcutaneous LD50: 3500mg/kg 2. Reproductive toxicity: female rat oral TDLo: 1800mg/kg, conception occurs after 2-19 days; femaleRat subcutaneous TDLo: 96g/kg, conception occurs after 11 days; Intravenous TDLo for female mice: 96mg/kg, conception occurs after 11-14 days

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 105.06

2. Molar volume (cm3/mol): 312.5

3. Isotonic specific volume (90.2K ): 855.5

4. Surface tension (dyne/cm): 56.1

5. Polarizability (10-24cm3): 41.65

Compute chemical data

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

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond acceptors: 6

4. Number of rotatable chemical bonds: 4

5. Number of tautomers: 6

6. Topological molecule polar surface area 101

7. Number of heavy atoms: 29

8. Surface charge: 0

9. Complexity: 827

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 7

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 yet

Storage method

This product should be sealed and stored in a cool, dry place.

Synthesis method

It can be produced by dehydrogenating hydrocortisone acetate using microorganisms or selenium dioxide

Purpose

Applicable to rheumatoid arthritis, rheumatic fever, lupus erythematosus, scleroderma, dermatomyositis, acute lymphoblastic leukemia, etc.

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Spironolactone sterol

Structural formula of spirolactone sterol

Structural formula

Business number 015D
Molecular formula C24H32O4S
Molecular weight 416.57
label

(7?,17?)-7-(acetylmercapto)-17-hydroxy-3-oxopregnant-4-en-21-carboxylic acid ?-lactone,

spironolactone,

Spironolactone

Numbering system

CAS number:52-01-7

MDL number:MFCD00082250

EINECS number:200-133-6

RTECS number:TU4725000

BRN number:None

PubChem number:24277736

Physical property data

1. Properties: White or off-white fine crystalline powder with a slight mercaptan odor and a slightly bitter taste.

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

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

4. Melting point (ºC): 202?208

5. Boiling point (ºC, normal pressure): 182?184

6. Boiling point (ºC, 5.2kPa) : Undetermined

7. Refractive index: Undetermined

8. Flash point (ºC): Undetermined

9. Specific rotation (º): -37

10. Autoignition point or ignition temperature (ºC): Not determined

11. Vapor pressure (kPa, 25ºC): Not determined

12 . Saturated vapor pressure (kPa, 60ºC): Undetermined

13. Heat of combustion (KJ/mol): Undetermined

14. Critical temperature (ºC): Undetermined

p>

15. Critical pressure (KPa): Undetermined

16. Log value of oil-water (octanol/water) partition coefficient: Undetermined

17. Explosion upper limit (%, V/V): Undetermined

18. Lower explosion limit (%, V/V): Undetermined

19. Solubility: Easily soluble in chloroform, benzene, Ethyl acetate, soluble in ethanol, insoluble in water.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

1. Molar refractive index: 112.68

2. Molar volume (cm3/mol): 335.7

3. Isotonic specific volume (90.2K ): 896.8

4. Surface tension (dyne/cm): 50.8

5. Polarizability (10-24cm3): 44.67

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): 2.9

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 10

6. Topological molecular polar surface area (TPSA): 60.4

p>

7. Number of heavy atoms?: 29

8. Surface charge: 0

9. Complexity: 818

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 7

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 yet

Storage method

None yet

Synthesis method

It can be synthesized from ethinyl androdiol through Grignard reaction, carboxylation, salt formation, hydrogenation, lactonization, oxidation, elimination, addition and other steps.

Purpose

It is a diuretic and has anti-aldosterone effect. It is used to treat liver disease and nephrotic edema related to excessive aldosterol. Preparations include tablets and capsules.

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