LACTIC ACID, DL-

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C3H6O3
Molecular Weight	90.0779
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of LACTIC ACID, DL-

Structure Search

SMILES

CC(O)C(O)=O

InChI

InChIKey=JVTAAEKCZFNVCJ-UHFFFAOYSA-N

InChI=1S/C3H6O3/c1-2(4)3(5)6/h2,4H,1H3,(H,5,6)

HIDE SMILES / InChI

Molecular Formula	C3H6O3
Molecular Weight	90.0779
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:14:55 UTC 2023` Edited by `admin` on `Fri Dec 15 15:14:55 UTC 2023`
Record UNII	3B8D35Y7S4
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

LACTIC ACID, DL-

Common Name

English

RACEMIC LACTIC ACID

Common Name

English

(±)-LACTIC ACID

Systematic Name

English

.ALPHA.-HYDROXYPROPIONIC ACID

Systematic Name

English

DL-LACTIC ACID [MI]

Common Name

English

LACTIC ACID (+-)

Common Name

English

.ALPHA.-HYDROXYPROPANOIC ACID

Systematic Name

English

ORDINARY LACTIC ACID

Common Name

English

ACIDUM LACTICUM [WHO-IP LATIN]

Common Name

English

INS-270

Code

English

LACTIC ACID, DL- [II]

Common Name

English

DL- Lactic acid [WHO-DD]

Common Name

English

LACTICUM ACIDUM [HPUS]

Common Name

English

PURAC FCC 88

Code

English

LACTICUM ACIDUM

Common Name

English

TONSILLOSAN

Common Name

English

(±)-2-HYDROXYPROPANOIC ACID

Systematic Name

English

E 270

Code

English

LUREX

Brand Name

English

NSC-367919

Code

English

E-270

Code

English

INS NO.270

Code

English

LACTIC ACID [JAN]

Common Name

English

PURAC FCC 80

Code

English

DL-LACTIC ACID

Common Name

English

HIPURE 88

Code

English

MILK ACID

Brand Name

English

LACTIC ACID [WHO-IP]

Common Name

English

Classification Tree Code System Code

CODEX ALIMENTARIUS (GSFA)

INS-270

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

JECFA EVALUATION

INS-270

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

CFR

21 CFR 862.1450

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

Code System Code Type Description

NSC

367919

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

RXCUI

1314409

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

RxNorm

DAILYMED

3B8D35Y7S4

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

SMS_ID

100000089031

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

WHO INTERNATIONAL PHARMACOPEIA

LACTIC ACID, DL-

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

Description: A colourless or slightly yellow, clear, syrupy, caustic liquid; odourless or with a slight characteristic odour. Miscibility: Miscible with water, ethanol (~750 g/l) TS, and ether R.Category: Used in the preparation of sodium lactate solution as electrolyte. Storage: Lactic acid should be kept in a tightly closed container.Additional information. Lactic acid as described is not suitable for parenteral administration (haemodialysis). Lactic acid is usuallya racemate (RS), but the (+)-(S)-isomer may predominate; it is hygroscopic. Requirement: Definition- Lactic acid is a mixture of lactic acid, its condensation products, and water, the equilibrium between the components being dependent on the concentration and temperature. Lactic acid contains not less than 88.0% m/mand not more than the equivalent of 92.0% m/mof C3H6O3.

CAS

50-21-5

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

CAS

598-82-3

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

SUPERSEDED

FDA UNII

3B8D35Y7S4

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

ECHA (EC/EINECS)

209-954-4

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

CAS

849585-22-4

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

SUPERSEDED

NCI_THESAURUS

C80130

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

NCI_THESAURUS

C45678

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

CONCEPT

Industrial Aid

EPA CompTox

DTXSID7023192

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

HSDB

800

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

PUBCHEM

612

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

CAS

152-36-3

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

SUPERSEDED

ECHA (EC/EINECS)

200-018-0

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

NON-SPECIFIC STEREOCHEMISTRY

MERCK INDEX

m6654

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

Merck Index

EVMPD

SUB22126

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

CAS

1334714-39-4

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

SUPERSEDED

DRUG BANK

DB04398

Created by admin on Fri Dec 15 15:14:55 UTC 2023 , Edited by admin on Fri Dec 15 15:14:55 UTC 2023

PRIMARY

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POTASSIUM LACTATE, DL-

SALT/SOLVATE -> PARENT

Related Record Type Details


					3B8D35Y7S4

LACTIC ACID, DL-

ACTIVE MOIETY