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MilliporeSigma

L1875

L-(+)-Lactic acid solution

30% in H2O (by weight)

Synonym(s):

(S)-2-Hydroxypropionic acid, Sarcolactic acid

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About This Item

Empirical Formula (Hill Notation):
C3H6O3
CAS Number:
79-33-4
Molecular Weight:
90.08
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
24896292
MDL number:
MFCD00064266
Beilstein/REAXYS Number:
1720251

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Product Name

L-(+)-Lactic acid solution, 30% in H2O (by weight)

InChI key

JVTAAEKCZFNVCJ-REOHCLBHSA-N

SMILES string

C[C@H](O)C(O)=O

InChI

1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m0/s1

concentration

30% in H2O (by weight)

solubility

water: soluble(lit.)

storage temp.

2-8°C

Quality Level

200

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This Item
6978027714L6402
L-(+)-Lactic acid solution 30% in H2O (by weight)

Sigma-Aldrich

L1875

L-(+)-Lactic acid solution

L-(+)-Lactic acid solution ~40% in H2O

Sigma-Aldrich

69780

L-(+)-Lactic acid solution

L-(+)-Lactic acid solution meets analytical specification of Ph. Eur., BP, 88-92% total acid basis

Sigma-Aldrich

27714

L-(+)-Lactic acid solution

L-(+)-Lactic acid BioXtra, ≥98% (titration)

Sigma-Aldrich

L6402

L-(+)-Lactic acid

solubility

water: soluble(lit.)

solubility

-

solubility

water: soluble(lit.)

solubility

H2O: 1 M at 20 °C, clear, colorless

Quality Level

200

Quality Level

100, 200

Quality Level

200

Quality Level

200

storage temp.

2-8°C

storage temp.

-

storage temp.

-

storage temp.

2-8°C

concentration

30% in H2O (by weight)

concentration

~40% in H2O

concentration

-

concentration

-

Application

L-(+)-Lactic acid solution may be used in the preparation of novel pH-sensitive physically crosslinked hydrogels.[1] It may be used in the preparation of low molecular weight poly(lactic acid) by direct polycondensation.[2]

Other Notes

Aqueous solutions of l(+)-Lactate.
Purity equivalent to L 1750.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

supp_hazards

EUH071

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
0000261475
0000360595
SLCF3387
0000360595
0000261475

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G G Jinesh et al.
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Robert J Mishur et al.
Aging cell, 15(2), 336-348 (2016-01-06)
Disruption of mitochondrial respiration in the nematode Caenorhabditis elegans can extend lifespan. We previously showed that long-lived respiratory mutants generate elevated amounts of α-ketoacids. These compounds are structurally related to α-ketoglutarate, suggesting they may be biologically relevant. Here, we show
Debby Gawlitta et al.
Journal of applied physiology (Bethesda, Md. : 1985), 103(2), 464-473 (2007-04-21)
Prolonged periods of tissue compression may lead to the development of pressure ulcers, some of which may originate in, for example, skeletal muscle tissue and progress underneath intact skin, representing deep tissue injury. Their etiology is multifactorial and the interaction
Young-Kyoung Lee et al.
The Journal of biological chemistry, 292(49), 20208-20217 (2017-10-06)
Impaired mitochondrial oxidative phosphorylation (OXPHOS) capacity, accompanied by enhanced glycolysis, is a key metabolic feature of cancer cells, but its underlying mechanism remains unclear. Previously, we reported that human hepatoma cells that harbor OXPHOS defects exhibit high tumor cell invasiveness
Synthesis and characterization of pH-sensitive hydrogels based on chitosan and D, L-lactic acid.
Qu X, et al.
Journal of Applied Polymer Science, 74(13), 3193-3202 (1999)
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