Lithium L-lactate
Lithium L-lactate (CAS: 27848-80-2; Formula: C3H5LiO3; MW: 96.01) is a lithium salt of L-lactic acid. It presents as a biochemical reagent within the carbohydrate and monosaccharide categories. This compound is suitable for various laboratory applications, research purposes, and potentially in specialised chemical synthesis where a lactate source with specific lithium counter-ion properties is required.
- IUPAC
- (S)-2-Hydroxypropionic acid lithium salt,L-Lactic acid lithium salt,Sarcolactic acid lithium salt
- Synonyms
- (S)-2-Hydroxypropionic acid lithium saltL-Lactic acid lithium saltSarcolactic acid lithium salt

Biochemical Research
Utilised as a reagent in biochemical studies, particularly those involving carbohydrate metabolism or studies requiring a specific chiral lactate source.
Chemical Synthesis
Serves as a building block or intermediate in the synthesis of more complex organic molecules and specialty chemicals.
Laboratory Reagent
Employed in general laboratory settings for analytical procedures or experimental protocols requiring a defined lithium salt of L-lactic acid.
| Molecular weight | 96.01 |
|---|---|
| Empirical formula | C3H5LiO3 |
| Assay | ≥98% (titration) |
| Storage temperature | 2-8°C |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Lithium L-lactate used for?
+
Lithium L-lactate is primarily used in biochemical research and as a general laboratory reagent. It can serve as a building block in chemical synthesis where a lithium salt of L-lactic acid is specifically needed.
What is the CAS number and chemical formula for Lithium L-lactate?
+
The CAS number for Lithium L-lactate is 27848-80-2 and its chemical formula is C3H5LiO3.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Lithium L-lactate with an assay of ≥98% by titration. We do not represent this product as USP, BP, EP, or any other pharmacopoeia grade unless explicitly stated in the product data.
How should Lithium L-lactate be handled and stored?
+
Handle Lithium L-lactate with appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. Store at refrigerated temperatures between 2-8°C.
Is Lithium L-lactate a controlled substance?
+
Based on the provided data, there is no indication that Lithium L-lactate (CAS: 27848-80-2) is a controlled substance.
How can I request a sample or quote for Lithium L-lactate?
+
Please contact our sales team through the website to request a sample or a detailed quotation for Lithium L-lactate.
How is Lithium L-lactate packed and shipped?
+
Lithium L-lactate is carefully packed to ensure product integrity during transit and is available for export globally through Tech Serve Solutions.
▶ Related products
![(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide (C8H13N3O4) — chemical structure, CAS 138472-01-2; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F138472-01-2.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(E)-hydroxyimino]-5-nitro-3-hexenamide
C8H13N3O4
Biochemicals & Reagents![(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide (C14H18N4O4) — chemical structure, CAS 162626-99-5; Biochemicals & Reagents, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F162626-99-5.png&w=3840&q=75)
(±)-(E)-4-Ethyl-2-[(Z)-hydroxyimino]-5-nitro-3-hexen-1-yl-nicotinamide
C14H18N4O4
Biochemicals & Reagents
(±)-2,5-Dimethoxy-4-bromoamphetamine hydrobromide
Biochemicals & Reagents

(±)-2-(p-Methoxyphenoxy)propionic acid
C10H12O4
Biochemicals & Reagents
(±)-2-Amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide
C10H13NO2·HBr
Biochemicals & Reagents
(±)-2-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxydecanoic acid
C10H20O3
Biochemicals & Reagents
(±)-3-Hydroxyoctanoic acid
C8H16O3
Biochemicals & Reagents▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis