ChemicalBook--->CAS DataBase List--->13794-15-5

13794-15-5

13794-15-5 Structure

13794-15-5 Structure
IdentificationBack Directory
[Name]

SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE
[CAS]

13794-15-5
[Synonyms]

Lactisol
Sweetness
FEMA 3773
Sweet pink
Sweetness inhibitor
Propanoic acid,2-(4-methoxyphe.
(±)-2-(p-Methoxyphenoxy)propionicaci
SODIUM2-(4-METHOXYPHENOXY)PROPANOATE
SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE
Propanoic acid, 2-(4-methoxyphenoxy)-
(+/-)-2-(p-Methoxyphenoxy)propionic acid
Cover sweet powder (inhibiting sweetener)
2-(4-METHOXYPHENOXY)PROPIONIC ACID SODIUM SALT
SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE USP/EP/BP
[EINECS(EC#)]

604-052-0
[Molecular Formula]

C10H12O4
[MDL Number]

MFCD07783974
[MOL File]

13794-15-5.mol
[Molecular Weight]

196.2
Chemical PropertiesBack Directory
[Melting point ]

92-94℃
[Boiling point ]

173-175 °C(Press: 1 Torr)
[density ]

1.185
[FEMA ]

3773 | SODIUM 2-(4-METHOXYPHENOXY)PROPANOATE
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Solid
[pka]

3.29±0.10(Predicted)
[color ]

Pale Brown to Brown
[biological source]

synthetic (organic)
[JECFA Number]

1029
[InChI]

1S/C10H12O4/c1-7(10(11)12)14-9-5-3-8(13-2)4-6-9/h3-7H,1-2H3,(H,11,12)
[InChIKey]

MIEKOFWWHVOKQX-UHFFFAOYSA-N
[SMILES]

COc1ccc(OC(C)C(O)=O)cc1
[LogP]

1.650 (est)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P302+P352-P305+P351+P338
[Hazard Codes ]

Xi,Xn
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[HS Code ]

2918999090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

2-(4-Methoxyphenoxy)propanoate is a potent inhibitor of the sweetness of sucrose and other sweeteners.
[Chemical Properties]

Lactisole, the sodium salt of racemic 2(4 methoxyphenoxy) propionic acid, is a sweet-taste inhibitor marketed by Domino Sugar. It was affirmed as a GRAS flavor (FEMA no. 3773). At a concentration of 100–150 ppm, lactisole eliminates the sweet taste of a 10% sugar solution. This inhibition appears to be receptor related because lactisole also inhibits the sweet taste of aspartame. The (S?) enantiomer [CAS: 4276-74-8] (38), isolated from roasted coffee beans, is the active isomer; the (R+) enantiomer is inert.
[Occurrence]

Reported found in coffee beans.
[Uses]

Sodium 2-(4-methoxyphenoxy)propanoic acid is a taste modulator that inhibits the perception of sweetness in humans, but not in rats.
[Definition]

ChEBI: (S)-2-(4-Methoxyphenoxy)propanoic acid is a carboxylic acid and an aromatic ether.
[Biochem/physiol Actions]

As a taste modulator, the sodium salt inhibits the perception of sweetness in humans, but not in rats.
[Synthesis]

Methyl 2-chloropropionate

17639-93-9

4-Methoxyphenol

150-76-5

SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE

13794-15-5

(1) Add p-methoxyphenol (10 kg), sodium hydroxide (10 kg), potassium iodide (0.12 kg) and water (100 kg) to the reaction vessel and stir for 30 minutes at room temperature. Subsequently, the reaction mixture was heated to 60°C and the temperature was maintained in the range of 60°C to 70°C. At this temperature, methyl 2-chloropropionate (11.85 kg) was added slowly and dropwise. The reaction was catalyzed by potassium iodide and p-methoxyphenol reacted with methyl 2-chloropropionate while sodium hydroxide continued to react with the resulting acid. The reaction temperature was maintained in the range of 60°C to 90°C. The reaction was carried out for 12 hours and then completed; (2) the reaction product was cooled to room temperature, and a 30% sulfuric acid solution was slowly added, and the addition of acid was stopped after adjusting the pH of the mixture to 2.0. Subsequently, the mixture was cooled to below 45°C and centrifuged to obtain white solid 2-(4-methoxyphenoxy)propionic acid (14.28 kg).

[References]

[1] Patent: US4760172, 1988, A
[2] Patent: CN103922923, 2016, B. Location in patent: Paragraph 0029; 0030
Spectrum DetailBack Directory
[Spectrum Detail]

SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE(13794-15-5)1HNMR
SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE(13794-15-5)IR1
SODIUM 2-(4-METHOXYPHENOXY)PROPIONATE(13794-15-5)IR2
13794-15-5 suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Telephone: 18210857532 18210857532
Website: https://www.jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Telephone: 4006356688 18621169109
Website: www.x-labseek.com/
Company Name: Shanghai Sphchem Co., Ltd.  
Telephone: 021-56491756 13512199871
Website: http://www.panhongchem.com
Company Name: Shanghai Topbiochem Technology Co., Ltd  
Telephone: 021-58170097
Website: www.topbiochem.com
Company Name: Wuxi Zhangkun Biochemical Technology Co., Ltd.  
Telephone: +86 0510-85629785
Website: www.chemicalbook.com/ShowSupplierProductsList16040/0_EN.htm
Company Name: Amatek Scientific Co. Ltd.  
Telephone: 0512-56316828 4008675858
Website: http://www.amateksci.com
Company Name: Shanghai Macklin Biochemical Co.,Ltd.  
Telephone: 15221275939 15221275939
Website: www.macklin.cn
Company Name: Nanjing Duolong Bio-tech Co.,Ltd.  
Telephone: 18905173768
Website: http://www.dolonchem.com
Company Name: Sigma-Aldrich  
Telephone: 021-61415566 800-8193336
Website: https://www.sigmaaldrich.cn
Company Name: Zhengzhou Guancheng Laboratory equipment Sales  
Telephone: 0371-88888888 qq272369594;2159423853qq
Website: https://www.chemicalbook.com/ShowSupplierProductsList16848/0_EN.htm
Company Name: Zhengzhou Alfachem Co.,Ltd.  
Telephone: 0371-53778726 18003825608
Website: show.guidechem.com/alfachem/
Company Name: Shanghai Qiao Chemical Science Co., Ltd  
Telephone: 021-58892003
Website: https://www.chemicalbook.com/supplier/10168672/1.htm
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Telephone: 15026964105
Website: www.shyuanye.com
Company Name: BePharm Ltd  
Telephone: 400-685-9117
Website: www.bepharm.com
Company Name: Shenzhen Simeiquan Biotechnology Co. Ltd  
Telephone: 18126413629 0755-23311925 2355327053
Website: www.chemicalbook.com/ShowSupplierProductsList19894/0_EN.htm
Company Name: Amadis Chemical Company Limited  
Telephone: 571-89925085
Website: http://www.amadischem.com
Company Name: Shenzhen Sendi Biological Technology Co., Ltd.  
Telephone: 18124570582 TEL:0755-23574479 2355327139
Website: www.chemicalbook.com/ShowSupplierProductsList19933/0_EN.htm
Company Name: Guangzhou Kafen Biotech Co.,Ltd  
Telephone: 18029243487 2355327168
Website: www.kafenchem.com
Tags:13794-15-5 Related Product Information
51338-27-3 69806-34-4 87237-48-7 94051-08-8 100646-51-3 175204-35-0