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35745

Supelco

1-Naphthaleneacetic acid

PESTANAL®, analytical standard

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Synonym(s):
α-Naphthaleneacetic acid, 1-Naphthylacetic acid, NAA
Empirical Formula (Hill Notation):
C12H10O2
CAS Number:
Molecular Weight:
186.21
Beilstein:
1308415
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

Assay

95-100% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

OC(=O)Cc1cccc2ccccc12

InChI

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

InChI key

PRPINYUDVPFIRX-UHFFFAOYSA-N

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This Item
N1641N0640317918
1-Naphthaleneacetic acid PESTANAL®, analytical standard

Supelco

35745

1-Naphthaleneacetic acid

1-Naphthylacetic acid 1 mg/mL, BioReagent, suitable for plant cell culture

Sigma-Aldrich

N1641

1-Naphthylacetic acid

product line

PESTANAL®

product line

BioReagent

product line

BioReagent

product line

-

assay

95-100% (HPLC)

assay

-

assay

≥95%

assay

≥90.0% (GC)

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

cell culture | plant: suitable

technique(s)

cell culture | plant: suitable

technique(s)

-

format

neat

format

-

format

-

format

-

shelf life

limited shelf life, expiry date on the label

shelf life

-

shelf life

-

shelf life

-

General description

1-Naphthaleneacetic acid is widely employed in agriculture as a synthetic plant hormone in the auxin family or a plant growth regulator, which can find applications in tissue culture.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Sigma-Aldrich International GmbH

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Example:

T1503
Product Number
-
25G
Pack Size/Quantity

Additional examples:

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

enter as 1.000309185)

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Flow-through optosensing of 1-naphthaleneacetic acid in water and apples by heavy atom induced-room temperature phosphorescence measurements
Fernandez-Arguelles TM, et al.
Talanta, 66(3), 696-702 (2005)
Auxins Regulations of Branched Spike Development and Expression of TFL, a LEAFY-Like Gene in Branched Spike Wheat (Triticum aestivum)
Yue W, et al.
Journal of Agricultural Science, 9(2), 27-27 (2017)
Peter Marhavý et al.
The EMBO journal, 32(1), 149-158 (2012-11-28)
Lateral root (LR) formation is initiated when pericycle cells accumulate auxin, thereby acquiring founder cell (FC) status and triggering asymmetric cell divisions, giving rise to a new primordium. How this auxin maximum in pericycle cells builds up and remains focused
Da Xiao et al.
Biochemical pharmacology, 84(2), 232-239 (2012-04-20)
Carboxylesterases (CES) constitute a class of hydrolytic enzymes that play critical roles in drug metabolism and lipid mobilization. Previous studies with a large number of human liver samples have suggested that the inducibility of carboxylesterases is inversely related with age.
Bin Han et al.
Plant science : an international journal of experimental plant biology, 184, 63-74 (2012-01-31)
Previous results revealed that haem oxygenase-1 (HO-1)/carbon monoxide (CO) system is involved in auxin-induced adventitious root formation. In this report, a cDNA for the gene ZmHO-1, encoding an HO-1 protein, was cloned from Zea mays seedlings. ZmHO-1 has a conserved

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