L1750
L-(+)-Lactic acid
≥98%
동의어(들):
(S)-2-Hydroxypropionic acid, Sarcolactic acid
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크기 선택
보기 변경
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C3H6O3
CAS 번호:
Molecular Weight:
90.08
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
201-196-2
Beilstein/REAXYS Number:
1720251
MDL number:
Assay:
≥98%
Quality Level
assay
≥98%
storage temp.
2-8°C
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
InChI key
JVTAAEKCZFNVCJ-REOHCLBHSA-N
General description
L-(+)-Lactic acid is the only naturally occurring lactic acid in humans and mammals. Commercially, few bacteria like Lactobacillus casei, L. delbrueckii, Streptococcus lactis produces L-Lactic acid by fermentation process. Lactic acid activates hydroxycarboxylic acid receptor, G-protein coupled receptor 81 (GPR81).
Application
Lactic acid has been used:
- as a component in substrate solution II for lactate dehydrogenase reaction
- as an additive in storage solution A
- as a supplement in the artificial gastric juice preparation for evaluation of degree of resistance Lactobacillus to the gastric stresses
Biochem/physiol Actions
L-(+)-Lactic acid is used as a substrate for lactic acid dehydrogenase and lactate oxidase.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1C
supp_hazards
저장 등급
8A - Combustible corrosive hazardous materials
flash_point_f
230.0 °F - closed cup
flash_point_c
110.00 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
문서
Explore gamma-valerolactone (GVL) as a greener solvent replacing DMF, NMP, and DMAc in organic synthesis with efficiency and low toxicity.
관련 콘텐츠
Product Information Sheet
International Union of Basic and Clinical Pharmacology. LXXXVIII. G protein-coupled receptor list: recommendations for new pairings with cognate ligands
Davenport AP, et al.
Pharmacological Reviews, 65(3), 967-986 (2013)
Cell-free transcription of SV40
SV40 protocols, 73-73 (2001)
A History of Lactic Acid Making: A Chapter in the History of Biotechnology (1990)