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TRIMETHYL CITRATE

Basic information Description Reference Safety Supplier Related

TRIMETHYL CITRATE Basic information

Product Name:
TRIMETHYL CITRATE
Synonyms:
  • 2,3-propanetricarboxylicacid,2-hydroxy-trimethylester
  • 3-Hydroxy-3-methoxycarbonylpentanedioic acid, dimethyl ester
  • Trimethyl 2-hydroxy-1,2,3-propanetricarboxylate
  • METHYL CITRATE
  • CITRIC ACID TRIMETHYL ESTER
  • 1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trimethyl ester
  • TRIMETHYL CITRATE
  • 2-Hydroxy-1,2,3-propanetricarboxylic acid trimethyl ester
CAS:
1587-20-8
MF:
C9H14O7
MW:
234.2
EINECS:
216-449-2
Product Categories:
  • Miscellaneous
  • Functional Materials
  • Hydroxycarboxylic Acid Esters (Plasticizer)
  • Plasticizer
  • C8 to C9
  • Carbonyl Compounds
  • Esters
Mol File:
1587-20-8.mol
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TRIMETHYL CITRATE Chemical Properties

Melting point:
75-78 °C
Boiling point:
176 16mm
Density 
1.3363 (rough estimate)
vapor pressure 
1.3hPa at 20℃
refractive index 
1.4455 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Sparingly), Methanol (Slightly)
form 
Solid
pka
10.43±0.29(Predicted)
color 
White to Off-White
Odor
at 100.00 %. ethereal fruity
Odor Type
ethereal
Water Solubility 
53.2g/L at 20℃
BRN 
1796169
LogP
0.7 at 20℃
CAS DataBase Reference
1587-20-8(CAS DataBase Reference)
EPA Substance Registry System
1,2,3-Propanetricarboxylic acid, 2-hydroxy-, trimethyl ester (1587-20-8)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
HS Code 
29181500

MSDS

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TRIMETHYL CITRATE Usage And Synthesis

Description

Trimethyl citrate is an ester of citric acid. It is a kind of non-toxic plasticizer1. Trimethyl citrate is one of the constituents of Dioscorea opposita2. The IC50 value for monoamine oxidase-B of trimethyl citrate was studied. It has various applications3: it can do the main flame retardant candle flame color, its melting point and can fully meet the flammability requirements of candle products. It can be used for the synthesis of pharmaceutical and pesticide. It can act as the main raw material for the production of citric acid hydrochloride, citric acid hydrochloride as well as the synthetic hot melt adhesive. It can also be used as the methyl methacrylate polymer a blowing agent, a stabilizer acrylamide, polyamide adhesive initiators, PVC plasticizers. It can also be used as solvent for household and II cleaner, film-former4.

Reference

  1. Huang, Li, L. I. Chun-Lian, and H. U. Qing-Guo. "Study on Catalytic Synthesis of Trimethyl Citrate by Solid Acid." Liaoning Chemical Industry (2012).
  2. https://www.sigmaaldrich.com/catalog/product/aldrich/27502?lang=en&region=US
  3. www.zhonglanindustry.com/product/trimethyl-citrate
  4. https://www.lookchem.com/Trimethyl-citrate/

Chemical Properties

Colorless crystals. M.P. 79℃. B.P. 287℃. (decomposes). Slightly soluble in water, soluble in alcohol and oils.

Uses

Trimethyl Citrate is a reagent used in the preparation of citrate-ciprofloxacin conjugates which has antibacterial activity.

Preparation

Trimethyl citrate is produced by direct esterification of Citric acid with Methanol using the old-fashioned method with 3% sulfuric acid and reflux to complete the esterification.

General Description

Trimethyl citrate is one of the constituents of Dioscorea opposita. The IC50 value for monoamine oxidase-B of trimethyl citrate was studied.

Flammability and Explosibility

Not classified

Synthesis

67-56-1

77-92-9

1587-20-8

(i) Synthesis of trimethyl citrate Citric acid (9.00 g, 46.8 mmol) was dissolved in anhydrous methanol and thionyl chloride (20.50 mL, 0.28 mol) was added slowly and dropwise at 0 °C and under nitrogen protection. The reaction mixture was stirred at 0 °C for 1 h, then warmed to room temperature and continued stirring overnight. Upon completion of the reaction, the volatile components were removed by distillation under reduced pressure. The resulting solid residue was recrystallized using a hexane/ethyl acetate solvent mixture to give 10.80 g of white crystalline trimethyl citrate in 98% yield. 1H NMR (acetone-d6, 200 MHz): δ 2.85 (dd, 4H, J1 = 15.4 Hz, J2 = 27.2 Hz); 3.60 (s, 6H); 3.72 (s, 3H); 4.50 (br.s, 1H). 13C NMR (acetone-d6): calculated value: M+ = 234.21.

References

[1] Molecules, 2006, vol. 11, # 4, p. 263 - 271
[2] Patent: WO2007/14471, 2007, A1. Location in patent: Page/Page column 30
[3] Patent: US2013/89611, 2013, A1. Location in patent: Paragraph 0133-0135
[4] Molecules, 2018, vol. 23, # 9,
[5] RSC Advances, 2014, vol. 4, # 100, p. 57297 - 57307

TRIMETHYL CITRATE Preparation Products And Raw materials

Preparation Products

TRIMETHYL CITRATESupplier

Jinan Daen Pharmaceutical Technology Co., Ltd Gold
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