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2-甲基琥珀酸

Methylsuccinic acid

CAS: 498-21-5

Molecular Formula: C5H8O4

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2-甲基琥珀酸 - Names and Identifiers

Name Methylsuccinic acid
Synonyms Methylsuccinic acid
2-Methylsuccinic acid
2-Methylbutanedioic acid
2-Propanedicarboxylic acid
1,2-Propanedicarboxylic acid
(plus-minus)-methylsuccinic acid
Methyl-Butanedioic acid Methylsuccinic acid Pyrotartaric acid
CAS 498-21-5
EINECS 207-857-1
InChI InChI=1/C5H8O4/c1-3(5(8)9)2-4(6)7/h3H,2H2,1H3,(H,6,7)(H,8,9)

2-甲基琥珀酸 - Physico-chemical Properties

Molecular FormulaC5H8O4
Molar Mass132.11
Density1.311g/cm3
Melting Point110-115℃
Boling Point236.5°C at 760 mmHg
Flash Point111.1°C
Water SolubilitySoluble in water.
Vapor Presure0.0162mmHg at 25°C
AppearanceWhite to light brown crystals
BRN1722946
pKa4.13(at 25℃)
Storage ConditionSealed in dry,Room Temperature
StabilityStable. Combustible. Incompatible with bases, oxidizing agents, reducing agents.
Refractive Index1.474
MDLMFCD00002659
Physical and Chemical Properties

Melting Point: 110 - 112

water-soluble: *** = 10g/100 mL at 22 C

Appearance: white or yellowish crystals

UsePharmaceutical Intermediates

2-甲基琥珀酸 - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
WGK Germany3
TSCAYes
HS Code29171900

2-甲基琥珀酸 - Upstream Downstream Industry

Raw MaterialsCarbon tetrachloride
Sodium cyanide
Barium hydroxide
Crotonic acid
Phenetole
Ethyl crotonate

2-甲基琥珀酸 - Uses and synthesis methods

overview

Methylsuccinic acid (methylene succinic acid) is a compound used for organic synthesis. It is prepared by fermentation under the liquid surface of Aspergillus terreus. It is a colorless, odorless, and moisture-absorbing crystal. Low toxicity, but its vapor is toxic. Easy to polymerize, can also be copolymerized with other monomers. This substance may be harmful to the environment, and special attention should be paid to water bodies.

physical and chemical properties

Appearance and properties: white to beige crystalline powder

Standard heat of combustion (enthalpy) of crystalline phase (kJ • mol-1):-2152.65

Crystal phase standard claimed heat (enthalpy)( kJ • mol-1):-958.22

Volatile: not volatile, can be decomposed by overheating

Solubility: Soluble in water, ethanol and acetone, slightly soluble in benzene, chloroform and ether

storage method

Keep the container closed. Store in a cool, dark place.

Molecular structure data

molar refractive index: 28.30

molar volume (cm3/mol):100.6

isometric ratio (90.2K):272.0

surface tension (dyne/cm):53.2

polarizability (10-24cm3):11.21

Calculated chemical data

1. Hydrophobic parameter calculation reference value (XlogP):-0.2

2. Number of hydrogen bond donors: 2

3. Number of hydrogen bond receptors: 4

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: None

6. Topological molecular polar surface area 74.6

7. Number of heavy atoms: 9

8. Surface charge: 0

9. Complexity: 129

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 structure centers: 0

14. Uncertain number of chemical bond structure centers: 0

15. Number of covalent bond units: 1

Preparation method

1. oxidation method. High temperature and high pressure are required, which takes a long time.

2. Ester hydrolysis method. The process is complicated, the operation steps are many, and the cost is high.

3. Catalytic hydrogenation method. Commonly used catalysts are: Cu catalyst, Pd catalyst, Ni catalyst, Pt, Rh catalyst

Main references

[1]http://baike.baidu.com/item/甲基丁二酸#7

[2] Wang Yingying, Gao Chuanhui, Wang Chuanxing, et al. Hydrogenation of itaconic acid to prepare methylsuccinic acid [J]. Journal of Qingdao University of Science and Technology (Natural Science Edition), 2014, 35(1):9-12.

chemical properties

White or yellowish crystals

use

for organic synthesis.

production method

using butenoic acid as raw material, it is prepared by the following steps. Butenoic acid and ethanol are mixed with carbon tetrachloride, sulfuric acid is added, reflux reaction is carried out for 12h, ethanol and carbon tetrachloride are recovered, and ethyl crotonate is obtained by salting out. Ethyl crotonate, ethanol and sodium cyanide aqueous solution were refluxed for 5h. Add barium hydroxide solution, concentrate to porridge under reduced pressure, and cool. Add nitric acid and react violently to release hydrogen cyanide gas. Concentrate to dry under reduced pressure, extract with benzene and ether to obtain crude product, and finally recrystallize with benzene and water once each to obtain the finished product.

Last Update:2024-04-09 21:21:28

2-甲基琥珀酸 - Nature

storage conditions Sealed in dry,Room Temperature
acidity coefficient (pKa) 4.13(at 25℃)
water solubility Soluble in water.
BRN 1722946
stability Stable. Combustible. Incompatible with bases, oxidizing agents, reducing agents.
NIST chemical information Butanedioic acid, methyl-(498-21-5)
EPA chemical information Butanedioic acid, 2-methyl- (498-21-5)
Last Update:2024-04-09 20:48:19
2-甲基琥珀酸
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View History
2-甲基琥珀酸
3-(4-羟苯基)丙酸甲酯
癸二酸丁二酯
(3-丙烯酰胺丙基)三甲基氯化铵
头孢地尼活性新酯
Raw Materials for 2-甲基琥珀酸
Carbon tetrachloride
Sodium cyanide
Barium hydroxide
Crotonic acid
Phenetole
Ethyl crotonate
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