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N4002

Sigma-Aldrich

2-Naphthaleneacetic acid

99%

Sinonimo/i:

2-Naphthylacetic acid

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About This Item

Formula condensata:
C10H7CH2CO2H
Numero CAS:
581-96-4
Peso molecolare:
186.21
Beilstein:
973396
Numero CE:
209-475-0
Numero MDL:
MFCD00004126
Codice UNSPSC:
12352100
ID PubChem:
24897359
NACRES:
NA.22

Livello qualitativo

100

Saggio

99%

Forma fisica

crystals

Punto di fusione

141-143 °C (lit.)

Stringa SMILE

OC(=O)Cc1ccc2ccccc2c1

InChI

1S/C12H10O2/c13-12(14)8-9-5-6-10-3-1-2-4-11(10)7-9/h1-7H,8H2,(H,13,14)
VIBOGIYPPWLDTI-UHFFFAOYSA-N

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCBM2486V
AR048151/1
048151/1
03824CE
04017AE

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Misaki Nakai et al.
Inorganic chemistry, 45(7), 3048-3056 (2006-03-28)
Two new dinuclear Ru(III) complexes containing naphthalene moieties, K[Ru2(dhpta)(mu-O2CCH2-1-naph)2] (1) and K[Ru2(dhpta)(mu-O2CCH2-2-naph)2] (2) (H5dhpta = 1,3-diamino-2-hydroxypropane-N,N,N',N'-tetraacetic acid, naph-1-CH2CO2H = 1-naphthylacetic acid, naph-2-CH2CO2H = 2-naphthylacetic acid), were synthesized. Complex 2 crystallized as an orthorhombic system having a space group of Pbca
T S Emudianughe et al.
Xenobiotica; the fate of foreign compounds in biological systems, 17(7), 823-828 (1987-07-01)
1. The influence of dose size upon the metabolic conjugation of 2-naphthylacetic acid with various amino acids and glucuronic acid has been studied in the guinea pig, mouse and hamster. 2. Guinea pigs conjugated 2-naphthylacetic acid with glycine and glucuronic
R Darío Falcone et al.
Langmuir : the ACS journal of surfaces and colloids, 20(14), 5732-5737 (2006-02-08)
The kinetics of hydrolysis of 2-naphthyl acetate (2-NA) catalyzed by alpha-chymotrypsin (alpha-CT), in reverse micellar solutions formed by glycerol (GY)-water (38% v/v) mixture/sodium bis(2-ethylhexyl)sulfosuccinate (AOT)/n-heptane has been determined by spectroscopic measurements. To compare the efficiency of this reaction with that
M V Marsh et al.
Xenobiotica; the fate of foreign compounds in biological systems, 11(10), 655-663 (1981-10-01)
1. 14C-Labelled benzoic acid, salicylic acid and 2-naphthylacetic acid were administered orally to horses, and urinary metabolites investigated by chromatographic and mass spectral techniques. 2. [14C]Benzoic acid (5 mg/kg) was eliminated rapidly in the urine, and quantitatively recovered in 24
K Palme et al.
Symposia of the Society for Experimental Biology, 44, 299-313 (1990-01-01)
To understand precisely the mechanisms by which hormones like auxins regulate plant differentiation and development, it is essential to isolate putative hormone receptors. We have purified the major auxin binding protein from maize coleoptiles to homogeneity. The protein has an
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