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Merck

L0625

Sigma-Aldrich

D-(−)-Lactic acid

≥90%

Synonim(y):

(R)-2-Hydroxypropionic acid

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About This Item

Wzór empiryczny (zapis Hilla):
C3H6O3
Numer CAS:
Masa cząsteczkowa:
90.08
Beilstein:
1720252
Numer WE:
Numer MDL:
Kod UNSPSC:
12352201
Identyfikator substancji w PubChem:
NACRES:
NA.25

Próba

≥90%

temp. przechowywania

−20°C

ciąg SMILES

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

InChI

1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)/t2-/m1/s1

Klucz InChI

JVTAAEKCZFNVCJ-UWTATZPHSA-N

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Zastosowanie

Lactic acid is used as a reagent in organic synthesis (in the manufacture of adhesives). It is used in the leather, textile, and tanning industries. It may be used as a plasticizer, a catalyst, or an acidifying agent. Lactic acid has even been used as a flavoring agent in the manufacture of tobacco products.

Działania biochem./fizjol.

In animals, lactic acid is a metabolic compound produced by proliferating cells and during anaerobic conditions such as strenuous exercise. Lactic acid can be oxidized back to pyruvate or converted to glucose via gluconeogenesis. Lactic acid is preferentially metabolized by neurons in several mammal species and during early brain development. D-lactate was utilized four times more slowly than L-lactate, but both isomers are absorbed at the same rate from the intestine.

Komentarz do analizy

Assayed enzymatically using D(−)lactic dehydrogenase
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Piktogramy

Corrosion

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

Eye Dam. 1 - Skin Corr. 1C

Zagrożenia dodatkowe

Kod klasy składowania

8A - Combustible corrosive hazardous materials

Klasa zagrożenia wodnego (WGK)

WGK 1

Środki ochrony indywidualnej

dust mask type N95 (US), Eyeshields, Gloves


Certyfikaty analizy (CoA)

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