Sodium (S)-lactate supplier

Name
Sodium (S)-lactate
EINECS 212-762-3
CAS No. 867-56-1
Article Data6
CAS DataBase
Density 1.33 g/cm³
Solubility Soluble in water
Melting Point 163-165 °C(lit.)
Formula C₃H₆O₃.Na
Boiling Point 227.6 °C at 760 mmHg
Molecular Weight 112.061
Flash Point 109.9 °C
Transport Information
Appearance liquid
Safety 24/25-36-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms (+)-Sodium lactate;Sodium L-(+)-lactate;SodiumL-lactate;Lacticacid, monosodium salt, L- (8CI);Propanoic acid, 2-hydroxy-, monosodium salt,(2S)- (9CI);Propanoic acid, 2-hydroxy-, monosodium salt, (S)-;(+)-Lactatesodium;
PSA 60.36000
LogP -1.88290

Synthetic route

: 113-24-6
sodium pyruvate

: 867-56-1
sodium L-lactate

Conditions

Conditions	Yield
enzymatic electrolysis;	70%
With L-lactate dehydrogenase from rabbit muscle; β-nicotinamide reduced form In phosphate buffer at 25℃; for 0.1h; pH=7.4; Kinetics; Further Variations:; Reagents; time;
With NAD; sodium formate; carbon co-immobilized lactate dehydrogenase and formate dehydrogenase In aq. buffer at 20℃; for 24h; Enzymatic reaction;

: 923031-01-0
L-menthyl L-lactoyl L-lactate

: 923031-02-1
L-menthyl L-lactoyl L-lactoyl L-lactate

A: 2216-51-5
(-)-menthol

B: 867-56-1
sodium L-lactate

C: 61597-98-6
(1R,2S,5R)-menthyl (S)-(-)-lactate

Conditions

Conditions	Yield
With sodium hydroxide; water In n-heptane at 15 - 60℃; for 0.6 - 3.6h; pH=11.65 - 14; Product distribution / selectivity;	A 5.95% B n/a C 51.71%

...Expand

: 302-84-1
serin

A: 246855-94-7
C3H6NO3(1-)*Na(1+)

B: 127-09-3
sodium acetate

C: 156-54-7
sodium butyrate

D: 867-56-1
sodium L-lactate

Conditions

Conditions	Yield
Stage #1: serin at 37℃; for 48h; pH=7.3 - 7.4; Microbiological reaction; aq. phosphate buffer; Inert atmosphere; Stage #2: With sodium hydroxide pH=9.5; aq. phosphate buffer; enantioselective reaction;

...Expand

: 79-33-4
L-Lactic acid

: 867-56-1
sodium L-lactate

Conditions

Conditions	Yield
With sodium hydroxide In tetrahydrofuran; methanol at 20℃; for 3h;

: (1S,2S,4S,5R)-(+)-(N-hexadecyl-5-vinyl-2-quinuclidinium)methanol bromide

: 867-56-1
sodium L-lactate

: 1357498-43-1
C3H5O3(1-)*C26H50NO(1+)

Conditions

Conditions	Yield
In methanol Reflux;	98%

: 1257384-39-6
2-(2-ethylbenzoimidazol-1-yl)-9-methyl-6-morpholin-4-yl-8-piperidin-4-yl-9H-purine hydrochloride

: 867-56-1
sodium L-lactate

: 1257385-44-6
(S)-1-(4-((2-(2-ethyl-1H-benzo[d]imidazol-1-yl)-9-methyl-6-morpholino-9H-purin-8-yl)methyl)piperidin-1-yl)-2-hydroxypropan-1-one

Conditions

Conditions	Yield
With 4-methyl-morpholine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 1h;	92%

: butyl [(1R,2S,5R)-(-)-menthoxymethyl]pyrrolidinium chloride

: 867-56-1
sodium L-lactate

: butyl [(1R,2S,5R)-(-)-menthoxymethyl]pyrrolidinium L-lactate

Conditions

Conditions	Yield
In acetone	89.5%

: methyl [(1R,2S,5R)-(-)-menthoxymethyl]pyrrolidinium chloride

: 867-56-1
sodium L-lactate

: methyl [(1R,2S,5R)-(-)-menthoxymethyl]pyrrolidinium L-lactate

Conditions

Conditions	Yield
In acetone	86.4%

: 16874-17-2
L-phenylalanine tert-butyl ester

: 867-56-1
sodium L-lactate

: 1309945-57-0
(S,S)-tert-butyl 2-[(2-hydroxypropanoyl)amino]-3-phenylpropanoate

Conditions

Conditions	Yield
With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere;	85%

: butyl [(1R,2S,5R)-(-)-menthoxyacetyl]pyrrolidinium chloride

: 867-56-1
sodium L-lactate

: butyl [(1R,2S,5R)-(-)-menthoxyacetyl]pyrrolidinium L-lactate

Conditions

Conditions	Yield
In acetone	84.4%

: 1018332-55-2
methyl [(1R,2S,5R)-(-)-menthoxyacetyl]pyrrolidinium chloride

: 867-56-1
sodium L-lactate

: methyl [(1R,2S,5R)-(-)-menthoxyacetyl]pyrrolidinium L-lactate

Conditions

Conditions	Yield
In acetone	84.1%

: 145707-12-6
Br(1-)*C22H46NO(1+)

: 867-56-1
sodium L-lactate

: 1357498-66-8
C3H5O3(1-)*C22H46NO(1+)

Conditions

Conditions	Yield
In methanol Reflux;	83%

: (1S,2R,4S,5R)-(+)-(N-hexadecyl-5-vinyl-2-quinuclidinium)methanol bromide

: 867-56-1
sodium L-lactate

: 1357498-51-1
C3H5O3(1-)*C26H50NO(1+)

Conditions

Conditions	Yield
In methanol Reflux;	82%

: 867-56-1
sodium L-lactate

: 31351-20-9, 57155-63-2, 116071-58-0
(-)-N-dodecyl-N-methylephedrinium bromide

: 1261244-81-8
C3H5O3(1-)*C23H42NO(1+)

Conditions

Conditions	Yield
In methanol Reflux;	80%
for 24h; Heating;	60%

: C10H8I3NO5S

: 867-56-1
sodium L-lactate

: 1245566-29-3
C13H12I3NO6

Conditions

Conditions	Yield
With 1H-imidazole In N,N-dimethyl acetamide at 40℃; for 10h; Product distribution / selectivity; Inert atmosphere;	76.7%

: 867-56-1
sodium L-lactate

: 3-(Benzyloxycarbonylamino)propyl 2,4-di-O-benzoyl-3-O-[2-O-benzoyl-4-O-methyl-3-O-(4-amino-2-O-benzoyl-3-O-methyl-β-D-quinovopyranosyl)-α-L-rhamnopyranosyl]-α-L-rhamnopyranoside hydrochloride

: 179601-57-1
3-(Benzyloxycarbonylamino)propyl 2,4-di-O-benzoyl-3-O-{2-O-benzoyl-4-O-methyl-3-O-[2-O-benzoyl-4-(L-2'-hydroxy)propionamido-3-methyl-β-D-quinovopyranosyl]-α-L-rhamnopyranosyl}-α-L-rhamnopyranoside

Conditions

Conditions	Yield
With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 1.5h; Ambient temperature;	75%

: 867-56-1
sodium L-lactate

: 75-36-5
acetyl chloride

: 36394-75-9
(S)-2-acetoxypropanoyl chloride

Conditions

Conditions	Yield
With hydrogenchloride; thionyl chloride In diethyl ether	64%

: 16652-71-4
benzyl (2S)-2-pyrrolidinecarboxylate hydrochloride

: 867-56-1
sodium L-lactate

: 89537-18-8
1-<(S)-2-hydroxy-1-oxopropyl>-L-proline phenylmethyl ester

Conditions

Conditions	Yield
With diphenylphosphoranyl azide; triethylamine In N,N-dimethyl-formamide for 24h; Ambient temperature;	60%

: 867-56-1
sodium L-lactate

: 41324-66-7
H-Pro-OBzl

: 89537-18-8
1-<(S)-2-hydroxy-1-oxopropyl>-L-proline phenylmethyl ester

Conditions

Conditions	Yield
With diphenylphosphoranyl azide; triethylamine In N,N-dimethyl-formamide for 24h; Ambient temperature;	60%

: rhodium(III) chloride trihydrate

: 867-56-1
sodium L-lactate

: (S)-(+)-Rh2{(HO)(CH3)CHCOO}4

Conditions

Conditions	Yield
In ethanol; water soln. of Rh salt added to soln. of the acid in 90% aq. EtOH (N2), refluxed (3 h, N2, color change from red to green), cooled (room temp.); ppt. filtered off, evapd., residue dissolved (abs. acetone), filtered, evapd., chromd. (silica gel, Et2O/EtOH); elem. anal.;	42%

: 1257384-82-9
2-(2-ethylbenzoimidazol-1-yl)-8-(3-methoxyazetidin-3-yl)-9-methyl-6-morpholin-4-yl-9H-purine

: 867-56-1
sodium L-lactate

: 1257385-29-7
(S)-1-(3-(2-(2-ethyl-1H-benzo[d]imidazol-1-yl)-9-methyl-6-morpholino-9H-purin-8-yl)-3-methoxyazetidin-l-yl)-2-hydroxypropan-1-one

Conditions

Conditions	Yield
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 18h;	23%

: 867-56-1
sodium L-lactate

: 36394-75-9
(S)-2-acetoxypropanoyl chloride

: 629-03-8
1 ,6-dibromohexane

: 867-56-1
sodium L-lactate

: 846588-11-2
C6 bis-L-lactate diol

Conditions

Conditions	Yield
In DMF (N,N-dimethyl-formamide) at 60℃; for 72h;
In N,N-dimethyl-formamide at 60℃; for 72h;

: 867-56-1
sodium L-lactate

: 138893-50-2
S-(-)-[2-(acetyloxy)]propionic acid sodium salt

Conditions

Conditions	Yield
With hydrogenchloride; sodium acetate; acetic anhydride In acetic acid

: 1044583-52-9
7'-(2-chlorophenyl)-6'-(4-chlorophenyl)-3',4'-dihydrospiro[cyclohexane-1,2'-pyrano[2,3-b]pyridin]-4'-amine

: 867-56-1
sodium L-lactate

A: 1044587-76-9
(2S)-N-[(S)-7'-(2-chlorophenyl)-6'-(4-chlorophenyl)-3',4'-dihydrospiro[cyclohexane-1,2'-pyrano[2,3-b]pyridin]-4'-yl]-2-hydroxypropanamide

B: 1044584-17-9
(2S)-N-[(R)-7'-(2-chlorophenyl)-6'-(4-chlorophenyl)-3',4'-dihydrospiro[cyclohexane-1,2'-pyrano[2,3-b]pyridin]-4'-yl]-2-hydroxypropanamide

Conditions

Conditions	Yield
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 0.5h;
With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 0.5h;

...Expand

: 5-(N-sulfinylamino)isophthalic acid dimethyl ester

: 867-56-1
sodium L-lactate

: 5-[(2S)-2-hydroxypropionyl]-isophthalic acid dimethyl ester

Conditions

Conditions	Yield
With 1,2,4-Triazole In N,N-dimethyl acetamide at 40℃; for 3h; Inert atmosphere;

: 67-56-1
methanol

: 867-56-1
sodium L-lactate

: 27871-49-4
(S)-Methyl lactate

Conditions

Conditions	Yield
With carbon dioxide at 165℃; under 21110.9 - 39353.1 Torr; for 1h; Product distribution / selectivity; Industry scale;

: C44H50EuN6O11P2(1-)*H(1+)

: 867-56-1
sodium L-lactate

: C44H50EuN6O11P2(1-)*C3H5O3(1-)*H(1+)*Na(1+)

Conditions

Conditions	Yield
In water at 21.84℃; pH=7.4;

: C39H45EuN5O7P2(1+)*Cl(1-)

: 867-56-1
sodium L-lactate

: C39H45EuN5O7P2(1+)*C3H5O3(1-)*Na(1+)*Cl(1-)

Conditions

Conditions	Yield
In methanol; water at 21.84℃; pH=7.4;

: 867-56-1
sodium L-lactate

: 113-24-6
sodium pyruvate

Conditions

Conditions	Yield
With Aerococcus viridans L-lactate oxidase, wild-type, containing oxidized-state FMN cofactor In aq. phosphate buffer at 20℃; pH=6.5; Kinetics; Reagent/catalyst; Temperature; Flow reactor;

Sodium (S)-lactate Specification

The CAS registry number of Sodium L-lactate is 867-56-1. Its EINECS registry number is 212-762-3. The IUPAC name is sodium (2S)-2-hydroxypropanoate. In addition, the molecular formula is C₃H₆O₃.Na and the molecular weight is 113.06. It is also called propanoic acid,2-hydroxy-,sodium salt(1:1),(2S)-. What's more, it is a kind of clear viscous liquid and belongs to the class of Inorganic & Organic Chemicals. Besides, it should be stored in sealed container, and placed in a cool and dry place.

Physical properties about Sodium L-lactate are: (1)ACD/LogP: -0.70; (2)ACD/LogD (pH 5.5): -2.76; (3)ACD/LogD (pH 7.4): -4.24; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 3; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 2; (11)Polar Surface Area: 46.53 Å²; (12)Flash Point: 109.9 °C; (13)Enthalpy of Vaporization: 53.96 kJ/mol; (14)Boiling Point: 227.6 °C at 760 mmHg; (15)Vapour Pressure: 0.015 mmHg at 25°C.

Uses of Sodium L-lactate: it can be used as pharmaceutical raw materials, and used in manufacturing of medicine. And it can be used as SAP and toughening agents for casein.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. During using it, wear suitable protective clothing and avoid contact with skin and eyes. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: [Na+].[O-]C(=O)[C@@H](O)C
(2)InChI: InChI=1/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1
(3)InChIKey: NGSFWBMYFKHRBD-CBXCQQQGBK

Product Name

Sodium (S)-lactate

Synthetic route

Sodium (S)-lactate Specification

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