L-cystine

L-cystine structural formula

Structural formula

Business number 0183
Molecular formula C6H12N2O4S2
Molecular weight 240.3
label

(R,R)-3,3′-dithiobis(2-aminopropionic acid),

Dithioaminopropionic acid,

Bis-beta-thioalanine,

disulfidealanine,

(R,R)-3,3′-Dithiobis(2-aminopropionicacid),

Cystine,

L-Dicysteine,

(R,R)-(-)Cystine,

L-cystinic acid,

biochemical reagents,

intermediates,

amino acids

Numbering system

CAS number:56-89-3

MDL number:MFCD00064228

EINECS number:200-296-3

RTECS number:HA2690000

BRN number:1728094

PubChem number:24893101

Physical property data

1. Properties: White hexagonal plate-shaped crystals or crystalline powder. Odorless and tasteless.

2. Density (g/mL, 25/4?): 1.677

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

4. Melting point (ºC): point 260~261? (decomposition)

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

6. Boiling point (ºC, 5.2kPa): Not determined

7. Refractive index: Not determined

8. Flash point (ºC): Not determined

9. Specific rotation (º): [?]D20 -223.4° (C=1, in 1mol/L hydrochloric acid).

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

11. Vapor pressure (kPa, 25ºC): Undetermined

12. Saturation 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: Soluble in dilute acid and alkaline solutions, Very slightly soluble in water, insoluble in ethanol, ether, benzene and chloroform.

Toxicological data

1. Acute toxicity: Rat oral LD50: 25mg/kg2.Other multiple dose toxicity: rat oral TDLo: 279mg/kg/93D-C

Ecological data

None yet

Molecular structure data

5. Molecular property data:

1. Molar refractive index: 55.95

2. Molar volume (cm3/mol): 152.8

3. Isotonic specific volume (90.2K): 468.6

4. Surface tension (dyne/cm): 88.2

5. Polarizability (10-24cm3): 22.18

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -6.3

2. Number of hydrogen bond donors: 4

3. Number of hydrogen bond acceptors: 8

p>

4. Number of rotatable chemical bonds: 7

5. Number of tautomers: none

6. Topological molecule polar surface area 177

7. Number of heavy atoms: 14

8. Surface charge: 0

9. Complexity: 192

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 2

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

1. Stable properties under normal temperature and pressure.

2. Found in tobacco leaves.

3. Widely found in hair, hair, bones and horns.

4. There are three isomers: left-handed body, right-handed body and racemate.

Storage method

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

Synthesis method

1. L-cystine was discovered in 1810 by Wollaston from bladder stones. In 1832, Berzelius named it cystine. It is a sulfur-containing amino acid that exists in small amounts in proteins, mostly in the keratin of hair, fingers and claws. It can also be obtained synthetically. Industrially extracted from hair, the yield can reach 7.5-8%. In actual production, some only reach 5%.
2.Hydrolyze pig hair in hydrochloric acid, filter to remove impurities, crystallize to obtain crude product, add activated carbon for decolorization and decolorizationPrepared from iron, washing and drying.

3.

Add 720kg of hydrochloric acid with a concentration of 10mol/L into the hydrolysis tank and heat it to 70~80?. Quickly add 400kg of human hair or pig, continue to heat to 100?, and raise the temperature to 110~117? within 1~1.5h, hydrolyze for 6.5~7h (from 100?), cool and filter. Add 30% to 40% industrial sodium hydroxide solution to the filtrate under stirring. When the pH value reaches 3.0, add alkali solution at a slow speed until the pH value is 4.8. Leave it for 36 hours, separate the precipitate, and centrifuge to dryness to obtain bladder. Crude acid product (I), the mother liquor contains glutamic acid, arginine and leucine, etc. Weigh 150kg of crude cystine (I), add about 90kg of 10mol/L hydrochloric acid and 360kg of water, heat to 65~70°C, stir and dissolve for 0.5h, then add 12kg of activated carbon, heat to 80~90°C, and keep warm for 0.5h. Plate and frame filter press. Heat the filtrate to 80-85°C, add 30% sodium hydroxide while stirring, and stop when the pH reaches 4.8. Let it stand for the crystals to precipitate, siphon the supernatant, separate the bottom precipitate, and then centrifuge and spin dry to obtain crude cystine (II). Weigh 100kg of crude cystine (II), add 500L of 1mol/L hydrochloric acid, heat to 70°C, and then add 3 to 5kg of activated carbon. Then the temperature was raised to 85°C, kept stirred for 0.5h, and plate and frame filtered. Add distilled water about 1.5 times the volume of the filtrate to the filtrate, heat it to 75-80°C, and neutralize it with 12% ammonia water to pH 3.5-4.0 while stirring. At this time, cystine crystals will precipitate. The crystals are centrifuged to dryness, washed with distilled water until there is no chloride ion, and vacuum dried to obtain the finished product of cystine. The yield of human hair can reach 8%, and the yield of pig hair can reach 5%.

Purpose

1. Used for biochemical research. Preparation of biological culture media. It is used in biochemistry and nutrition research. In medicine, it can promote the oxidation and reduction functions of body cells, increase white blood cells and prevent the development of pathogenic bacteria. Mainly used for various types of alopecia. It is also used for acute infectious diseases such as dysentery, typhoid, and influenza, asthma, neuralgia, eczema, and various poisoning diseases, and has the effect of maintaining protein configuration. Also used as food flavoring.

2.Biochemical reagents, used for the preparation of biological culture media. It is also an important component of amino acid infusion and complex amino acid preparations.

3.Used as feed nutritional fortifier, it is beneficial to animal development, increases body weight and liver and kidney function, and improves fur quality.

4.Can be used as a cosmetic additive, which can promote wound healing, prevent skin allergies and treat eczema.

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L-cystathionine

L-cystathionine structural formula

Structural formula

Business number 0182
Molecular formula C7H14N2O4S
Molecular weight 222.26
label

(R)-S-(2-amino-2-carboxyethyl)-L-cysteine,

(R)-S-(2-Amino-2-carboxyethyl)-L-homocysteine

Numbering system

CAS number:56-88-2

MDL number:MFCD00036685

EINECS number:200-295-8

RTECS number:None

BRN number:2505200

PubChem number:24892965

Physical property data

1. Character: Crystal.


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


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


4. Melting point (ºC): 240 ?250??262~263?).


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


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


7. Refractive index: not OK


8. Flashpoint (ºC): Undetermined


9. Specific optical rotation ( º): Undetermined


10. Spontaneous ignition point or ignition Combustion temperature (ºC): not OK


11. Vapor Pressure (kPa,25ºC): Undetermined


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. Oil and water (octanol /Water) partition coefficient pair Value: Undetermined


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


18. Lower explosion limit (%,V/V): not OK


19. Solubility: Not available Sure.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data

5. Molecular property data:


1. Molar refractive index: 52.59


2. Molar volume (m3/mol??155.4


3. Isotonic specific volume (90.2K):457.7


4. Surface Tension (dyne/cm):75.2


5. Polarizability?10-24cm3): 20.84

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): -6


2. Number of hydrogen bond donors: 4


3. Number of hydrogen bond acceptors: 6


4. Number of rotatable chemical bonds: 7


5. Number of tautomers:


6. Topological molecular polar surface area (TPSA):127


7. Number of heavy atoms: 14


8. Surface charge: 0


9. Complexity: 212


10. Number of isotope atoms: 0


11. Determine the number of atomic stereocenters: 2


12. The number of uncertain atomic stereocenters: 0


13. Determine the number of stereocenters of chemical bonds: 0


14. Uncertain number of chemical bond stereocenters: 0


15. Number of covalent bond units: 1

Properties and stability

None yet

Storage method

This product should be kept sealed.

Synthesis method

Generated by the interaction of o-succinyl homoserine and cysteine. Cystathionine is cystathionine betaLyase removes pyruvate and NH3generates homocysteine.

Purpose

For biochemical research.

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Isoeugenol

isoeugenol structural formula

Structural formula

Business number 02CB
Molecular formula C10H12O2
Molecular weight 164.20
label

2-methoxy-4-propenylphenol,

4-hydroxy-3-methoxypropenylbenzene,

2-methoxy-4-propenylphenol,

4-propenylguaiacol,

2-Methoxy-4-propenylphenol,

4-Hydroxy-3-methoxypropenylbenzene,

4-Propenylguaiacol

Numbering system

CAS number:97-54-1

MDL number:MFCD00009285

EINECS number:202-590-7

RTECS number:SL7875000

BRN number:1909602

PubChem number:24881222

Physical property data

  1. Characteristics: light yellow liquid with a clove-like smell.
  2. Density (g/mL, 20?): 1.079~1.0851
  3. Relative vapor density (g/mL, air=1): Undetermined
  4. Melting point (ºC): -10
  5. Boiling point (ºC, normal pressure): 268
  6. Boiling point (ºC, KPa): Undetermined
  7. Refractive index (n20D): 1.575
  8. Flash point (ºC): 112
  9. Specific rotation ( º): Not determined
  10. Autoignition point or ignition temperature (ºC): Not determined
  11. Vapor pressure (mmHg, 20ºC): <0.01
  12. Saturated vapor Pressure (kPa, 25ºC): 0.093
  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: Slightly soluble in water, soluble in ethanol, ether, chloroform, and propylene glycol.

Toxicological data

1. Skin/eye irritation: Standard Dresser test: Male skin contact, 16mg/48HREACTION SEVERITY, moderate reaction; Standard Dresser test: Rabbit skin contact, 100mg/24HREACTION SEVERITY, strong reaction; Standard Dresser test: Guinea pig skin contact, 100mg/24HREACTION SEVERITY, strong reaction; 2. Acute toxicity: Rat oral LD50: 1560mg/kg; Mouse peritoneal cavity LD50: 328mg/kg; Guinea pig oral LD50: 1410mg/kg; 3. Mutagenicity Properties: Sister chromatid exchange experiment: human lymphocytes, 250 ?mol/L;

Ecological data

This substance may be harmful to the environment and it is recommended not to let it enter the environment.

Molecular structure data

1. Molar refractive index: 50.70

2. Molar volume (cm3/mol): 152.8

3. Isotonic specific volume (90.2K ): 381.9

4. Surface tension (dyne/cm): 38.9

5. Polarizability (10-24cm3): 20.10

Compute chemical data

1. Hydrophobic parameter calculation reference value (XlogP): 2.6

2. Number of hydrogen bond donors: 1

3. Number of hydrogen bond acceptors: 2

4. Number of rotatable chemical bonds: 2

5. Number of tautomers: 3

6. Topological molecular polar surface area (TPSA): 29.5

p>

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 154

10. Number of isotope atoms : 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the chemical bond configuration Number of centers: 1

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Avoid contact with strong oxidants.

2. Exist in oriental tobacco leaves and tobacco leaves.

3. Exist in nutmeg oil, ylang-ylang oil, etc.

4. There are two isomers, cis and trans, which have allergic effects at high concentrations. The dosage in consumer products that do not come into contact with the skin should not exceed 0.5%.

Storage method

Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. Keep container sealed and strictly prohibited from contact with air. should be kept away from oxidizer, do not store together. Equipped with the appropriate variety and quantity of fire equipment. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Obtained from the isomerization of eugenol by heating in potassium hydroxide solution. Treat eugenol or eugenol-rich essential oils with a potassium hydroxide solution to convert it into a salt. It is then heated to isomerize. After cooling, use dilute sulfuric acid to decompose the alkali metal salt, free isoeugenol, wash with water, dry, and distill under reduced pressure to obtain the finished product. Isoeugenol is found naturally in ylang ylang oil and nutmeg oil. In addition to the preparation method of eugenol isomerization, it is also prepared industrially by the synthesis method of safrole or isosafrole.

2. Heat the amyl alcohol solution of eugenol and potassium hydroxide to 200-230°C, then pour it into water, acidify it with inorganic acid, and distill the precipitated oil layer to obtain the fine product.

3. Tobacco: OR, 26; synthesis: obtained by heating eugenol and potassium solution.

Purpose

It is more elegant than eugenol for blending. It is often used as the main agent of carnation essence. It is also widely used in various other floral essences. It is very stable as a fragrance for cosmetics and soaps. It is also used as a food flavoring for apples, grapes, plums, apricots, raspberries or walnuts. It also has applications in dental medicine. In industry, vanillin is generally produced by oxidation of isoeugenol.

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PRODUCT