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317918

Sigma-Aldrich

1-Naphthaleneacetic acid

technical grade

Synonym(s):

α-Naphthaleneacetic acid, 1-Naphthylacetic acid, NAA

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About This Item

Empirical Formula (Hill Notation):
C12H10O2
CAS Number:
86-87-3
Molecular Weight:
186.21
Beilstein/REAXYS Number:
1308415
EC Number:
201-705-8
MDL number:
MFCD00004046
UNSPSC Code:
12352100
PubChem Substance ID:
24859106
NACRES:
NA.22

grade

technical grade

Quality Level

100

assay

≥90.0% (GC)

form

lumps
powder

functional group

carboxylic acid

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

Gene Information

human ... CCKAR(886) , CCKBR(887)

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Related Categories

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF8042
BCCF1407
BCCD4232
BCCD3555
MKCJ7427

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The microRNA miR393 has been shown to play a role in plant development and in the stress response by targeting mRNAs that code for the auxin receptors in Arabidopsis. In this study, we verified that two rice auxin receptor gene
Tobias Kretzschmar et al.
Nature, 483(7389), 341-344 (2012-03-09)
Strigolactones were originally identified as stimulators of the germination of root-parasitic weeds that pose a serious threat to resource-limited agriculture. They are mostly exuded from roots and function as signalling compounds in the initiation of arbuscular mycorrhizae, which are plant-fungus
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BMC plant biology, 12, 160-160 (2012-09-12)
Plant cytosolic ribosomal proteins are encoded by small gene families. Mutants affecting these genes are often viable, but show growth and developmental defects, suggesting incomplete functional redundancy within the families. Dormancy to growth transitions, such as the activation of axillary
P B Nagabalasubramanian et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82(1), 169-180 (2011-08-09)
In this work, the FT-IR and FT-Raman spectra of 1-naphthaleneacetic acid methyl ester (abbreviated as 1-NAAME, C(10)H(7)CH(2)CO(2)CH(3)) have been recorded in the region 3600-10 cm(-1). The optimum molecular geometry, normal mode wavenumbers, infrared and Raman intensities, Raman scattering activities, corresponding
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Global Trade Item Number

SKUGTIN
317918-500G
317918-100G4061835052264

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