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4316-73-8

Basic Information
CAS No.: 4316-73-8
Name: Sodium sarcosinate
Article Data: 5
Molecular Structure:
Molecular Structure of 4316-73-8 (Sodium sarcosinate)
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
Appearance: clear liquid
Risk Codes: R36/37/38
PSA: 52.16000
LogP: -1.65340
Synthetic route
109-83-1

(2-hydroxyethyl)(methyl)amine

4316-73-8

sodium sarcosinate

Conditions
ConditionsYield
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.
107-97-1

sarcosine

4316-73-8

sodium sarcosinate

Conditions
ConditionsYield
With ammonia; sodium
5616-32-0

(methylamino)acetonitrile

4316-73-8

sodium sarcosinate

Conditions
ConditionsYield
With sodium hydroxide at 75℃; for 4h; Temperature; Large scale;
3926-62-3

sodium monochloroacetic acid

74-89-5

methylamine

4316-73-8

sodium sarcosinate

Conditions
ConditionsYield
at 10 - 200℃; under 836.056 - 228015 Torr; Flow reactor;
2767-80-8

tris(hydroxymethyl)phosphine

4316-73-8

sodium sarcosinate

tris(N-methyl-N-sodiumcarboxylatomethylaminomethyl)phosphine

Conditions
ConditionsYield
In water at 20℃; for 1h; Condensation;99%
4316-73-8

sodium sarcosinate

79-11-8

chloroacetic acid

71160-37-7

sodium methyliminodiacetate

Conditions
ConditionsYield
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%
4316-73-8

sodium sarcosinate

oleic acid chloride

110-25-8

N-oleoylsarcosine

Conditions
ConditionsYield
With water; sodium hydroxide In toluene at 30℃; for 1h; Solvent;97.8%
2M-NaOH

2M-NaOH

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
ConditionsYield
With hydrogenchloride90.5%
156-62-7

calcium cyanamide

4316-73-8

sodium sarcosinate

57-00-1

Creatinine

Conditions
ConditionsYield
With phosphoric acid; sulfuric acid86%
phosphoric acid75%
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
ConditionsYield
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 %.

Sodium sarcosinate can react with 2-chloro-1,3,5-trinitro-benzene to get N-methyl-N-(2,4,6-trinitrophenyl)glycine.

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