calcium carbide

Calcium carbide structural formula

Structural formula

Business number 01J6
Molecular formula CaC2
Molecular weight 64.10
label

Carbide Level 4,

calcium carbide,

Calcium acetylide,

Acetylenogen,

other

Numbering system

CAS number:75-20-7

MDL number:MFCD00010905

EINECS number:200-848-3

RTECS number:None

BRN number:3909011

PubChem number:24856368

Physical property data

1. Characteristics: Colorless crystals, industrial products are gray-black lumps, and the cross-section is purple or gray. [1]

2. Melting point (?): 2300[2]

3. Boiling point (?): decomposition [3]

4. Relative density (water = 1): 2.22[4]

5. Octanol/ Water distribution coefficient: -0.30[5]

6. Ignition temperature (?): >325[6]

7.Solubility: No data yet

Toxicological data

1. Acute toxicity No data available

2. Irritation No data available

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradability No information available

4. Other harmful effects[7] This substance is harmful to the environment and should be specially Pay attention to water pollution.

Molecular structure data

None yet

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: 5

4. Number of rotatable chemical bonds: 8

5. Number of tautomers: none

6. Topological molecule polar surface area 61.8

7. Number of heavy atoms: 18

8. Surface charge: 0

9. Complexity: 271

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 1

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. Stability[8] Stable

2. Incompatible substances[9] Water, alcohols, acids

3. Conditions to avoid contact[10] Humid air

4. Hazards of aggregation[11] No aggregation

Storage method

Storage Precautions[12] Store in a cool, dry and well-ventilated special warehouse with a temperature not exceeding 32°C and a relative humidity not exceeding 75%. Keep away from fire and heat sources. The packaging must be sealed and protected from moisture. It should be stored separately from acids, alcohols, etc. and avoid mixed storage. The storage area should be equipped with appropriate? materials to contain spills.

Synthesis method

1. The electric furnace reduction method is currently the only method for industrial production of calcium carbide. This method was industrialized in the United States as early as 1895. The production involves high-temperature operations, a lot of dust, and high power consumption. Improvements in the process can improve operating conditions, reduce heat loss, and increase carbon monoxide recovery and utilization. Closed and large-scale Calcium carbide furnace. Crush the coke and lime, mix them evenly according to the proportion, add them to a closed calcium carbide furnace, heat them with electricity, and perform a reduction reaction at 2000-2200°C to generate molten calcium carbide, which flows from the furnace into a calcium carbide pot for cooling, crushing, and packaging. kg/ton of coke (84% fixed carbon) 550 limestone (CaO92%) 840 electrode paste 30 electricity 3200 (degree/ton)

2. Calcium carbide can be directly produced from the two elements of carbon and metallic calcium in an electric arc furnace Synthetically, or by reacting calcium oxide and carbon in an electric arc furnace at a high temperature of 2000°C. The purity of the products produced by these two methods is not high. The purity of calcium carbide produced by heating calcium cyanamide CaCN2 or calcium cyanamide and carbon in high vacuum can reach 99%.

The alumina boat is filled with pure calcium cyanamide or a mixture of calcium cyanamide and acetylene carbon black (or sugar charcoal), and the boat is placed in a ground-mouthed high-aluminum vessel with one end closed. To make porcelain tubes, this tube is connected to a vacuum pump and heated with a molybdenum wire furnace.

Heating CaCN2 or the mixture of CaCN2 and C must be carried out in two steps: the first step is to heat to 1100~1150? for 2~3 hours in high vacuum to fully decompose CaCN2 and remove as much N2 as possible. At this time, care should be taken to control the temperature not to exceed 1150°C to avoid the formation of a CaCN2?CaC2 eutectic at 1170°C. In the second step, continue to raise the temperature to 1350°C for 1 hour, remove the remaining N2, and obtain pure white calcium carbide. Purity reaches 99%.

Attached is the preparation method of calcium cyanamide. Pure HCN is dried by CaCl2 and P2O5 and condensed in a low-temperature receiver. The collection amount should be equal to 3 times the calculated amount. Put CaCO3 in a porcelain boat, place the porcelain boat in a porcelain tube, and heat the porcelain tube to 700~850°C. Then warm the HCN receiver to 18°C. N2 gas mixed with a small amount of NH3 is used to carry HCN through CaCO3, and pure white CaCN2 can be obtained after 3 hours, with a purity of 99.4%.

Purpose

1. About 60% of calcium carbide is used in chemical production, and the remaining 40% is used in metal welding and cutting. A series of chemical products can be produced using calcium carbide as raw materials, such as PVC resin, polyvinyl alcohol, vinyl acetate, chloroprene rubber, butanol, octanol, tricyanethylene, tetracyanoethylene, acetaldehyde, acetylene carbon black, lime nitrogen, etc. . The largest consumption is the production of PVC resin, accounting for 60% of the consumption of calcium carbide for chemical industry. Calcium carbide powder is irritating and can damage the skin and respiratory system.

2. It is an important basic chemical raw material, mainly used to produce acetylene gas and calcium cyanamide. Also used in organic synthesis, etc. [13]

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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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