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| CAS No.: | 4316-73-8 |
|---|---|
| Name: | Glycine, N-methyl-,sodium salt (1:1) |
| Article Data: | 5 |
| Cas Database | |
| Molecular Structure: | |
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| Formula: | C3H6NNaO2 |
| Molecular Weight: | 111.076 |
| Synonyms: | Sarcosine, monosodium salt (8CI);Sarcosinesodium salt;Sodium (methylamino)acetate;Sodium N-(methylamino)acetate;Sodium N-methylglycinate;Glycine,N-methyl-, monosodium salt (9CI); |
| EINECS: | 224-338-5 |
| Density: | 1.2 g/cm3 |
| Melting Point: | > 0oC |
| Boiling Point: | 195.1 °C at 760 mmHg |
| Flash Point: | 71.8 °C |
| Solubility: | N/A |
| Appearance: | clear liquid |
| Hazard Symbols: | N/A |
| Risk Codes: | R36/37/38 |
| Safety: | |
| Transport Information: | N/A |
| PSA: | 52.16000 |
| LogP: | -1.65340 |
- 431-67-41,1-Dibromo-3,3,3-trifluoroacetone
- 4316-74-9Ethanesulfonic acid,2-(methylamino)-, sodium salt (1:1)
- 43167-79-92,4-BIS(ANILINO)-6-(4-MORPHOLINO)-1,3,5-TRIAZINE, 97%
- 4316-93-2Pyrimidine,4,6-dichloro-5-nitro-
- 4316-94-34-Pyrimidinamine,6-chloro-5-nitro-
- 4316-97-6Pyrimidine,4,6-dichloro-5-methyl-
- 4316-98-74,5-Pyrimidinediamine,6-chloro-
- 43170-96-3Imidazo[1,2-a]pyridine-2-ethanamine
- 431-72-1Trifluoropyruvic acid, monohydrate
- 4317-79-71,3-Propanediamine,N1-tetradecyl-
| Conditions | Yield |
|---|---|
| With sodium hydroxide; Cu/Ni Raney catalyst In water at 160℃; under 7500.75 Torr; for 4h; | 97.2% |
| With (6-di-tert-butylphosphinomethyl-2,2’-bipyridyl)Ru(CO)HCl; water; sodium hydroxide In 1,4-dioxane for 24h; Schlenk technique; Inert atmosphere; Glovebox; Reflux; | > 99 %Spectr. |
| Conditions | Yield |
|---|---|
| With ammonia; sodium |
| Conditions | Yield |
|---|---|
| With sodium hydroxide at 75℃; for 4h; Temperature; Large scale; |
| Conditions | Yield |
|---|---|
| at 10 - 200℃; under 836.056 - 228015 Torr; Flow reactor; |
| Conditions | Yield |
|---|---|
| In water at 20℃; for 1h; Condensation; | 99% |
| Conditions | Yield |
|---|---|
| Stage #1: sodium sarcosinate; chloroacetic acid With sodium iodide In water at 20℃; for 1h; Large scale; Stage #2: With sodium hydroxide In water at 55 - 90℃; for 4.5h; pH=8.5 - 9; Large scale; | 98% |
| Conditions | Yield |
|---|---|
| With water; sodium hydroxide In toluene at 30℃; for 1h; Solvent; | 97.8% |
- 107-97-1
sarcosine
- 617-09-4
di-o-tolyl carbonate
- 4316-73-8
sodium sarcosinate
- 116714-27-3
N-methoxycarbonyl-N-methyl-glycine
| Conditions | Yield |
|---|---|
| With hydrogenchloride | 90.5% |
| Conditions | Yield |
|---|---|
| With phosphoric acid; sulfuric acid | 86% |
| phosphoric acid | 75% |
| sulfuric acid |
- 7703-74-4
2,6-bis-(bromomethyl)pyridine
- 4316-73-8
sodium sarcosinate
- 146448-83-1
N,N'-<(pyridine-2,6-diyl)bis(methylene)>bis
| Conditions | Yield |
|---|---|
| With sodium hydroxide In methanol for 13h; Heating; | 85% |
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Specification
The Sodium sarcosinate, with the CAS registry number 4316-73-8, is also known as N-Methylglycine monosodium salt. Its EINECS registry number is 224-338-5. This chemical's molecular formula is C3H6NNaO2 and molecular weight is 111.08. What's more, its IUPAC name is called Sodium 2-(methylamino)acetic acid. It should be stored in a cool, dry and well-ventilated place. This chemical can be prepared by formaldehyde, hydrocyanic acid and methylamine.
Physical properties about Sodium sarcosinate are: (1)ACD/LogP: -0.793; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -3.29; (4)ACD/LogD (pH 7.4): -3.29; (5)ACD/BCF (pH 5.5): 1.00; (6)ACD/BCF (pH 7.4): 1.00; (7)ACD/KOC (pH 5.5): 1.00; (8)ACD/KOC (pH 7.4): 1.00; (9)#H bond acceptors: 3; (10)#H bond donors: 2; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 40.54 Å2; (13)Flash Point: 71.8 °C; (14)Enthalpy of Vaporization: 47.54 kJ/mol; (15)Boiling Point: 195.1 °C at 760 mmHg; (16)Vapour Pressure: 0.184 mmHg at 25 °C.
Uses of Sodium sarcosinate: (1) it is used as cosurfactant, dyeing auxiliary and biochemical reagent; (2) it is used to produce other chemicals. For example, it can react with 2-chloro-1,3,5-trinitro-benzene to get N-methyl-N-(2,4,6-trinitrophenyl)glycine. The reaction occurs with solvents methanol and H2O. The reaction time is 20 min. The yield is 70 %.
You can still convert the following datas into molecular structure:
(1) SMILES: [Na+].[O-]C(=O)CNC
(2) InChI: InChI=1S/C3H7NO2.Na/c1-4-2-3(5)6;/h4H,2H2,1H3,(H,5,6);/q;+1/p-1
(3) InChIKey: ZUFONQSOSYEWCN-UHFFFAOYSA-M