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521949

3-Iodo-2-propynyl N-butylcarbamate

97%

Synonym(s):

1-Iodoprop-1-yn-3-yl N-n-butylcarbamate, 3-Iodoprop-2-yn-1-yl N-butylcarbamate, 3-Iodoprop-2-yn-1-yl butylcarbamate, 3-Iodopropargyl n-butylcarbamate

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About This Item

Linear Formula:
CH3(CH2)3NHCO2CH2C≡Cl
CAS Number:
55406-53-6
Molecular Weight:
281.09
NACRES:
NA.22
PubChem Substance ID:
24874236
UNSPSC Code:
12352100
EC Number:
259-627-5
MDL number:
MFCD00072438
Assay:
97%
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Quality Level

100

assay

97%

mp

64-68 °C (lit.)

functional group

amine, iodo

SMILES string

CCCCNC(=O)OCC#CI

InChI

1S/C8H12INO2/c1-2-3-6-10-8(11)12-7-4-5-9/h2-3,6-7H2,1H3,(H,10,11)

InChI key

WYVVKGNFXHOCQV-UHFFFAOYSA-N

General description

3-Iodo-2-propynyl N-butylcarbamate is also referred to as iodopropynyl butylcarbamate (IPBC). It is widely used as antifungal and anti-microbial agent. IPBC can be encapsulated in polystrene/polycaprolactone blend in the form microspheres. The microspheres were tested for invitro antifouling activity.

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Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Sens. 1 - STOT RE 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ9477
MKCR1844
MKCS2994
MKCS5975
MKCQ5573

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Charlotte Devantier Jensen et al.
Contact dermatitis, 48(3), 155-157 (2003-05-21)
3-Iodo-2-propynyl-butylcarbamate (IPBC) is a fungicide used in both industrial products and cosmetics. We report the first case of allergic contact dermatitis from airborne exposure to this preservative. A 34-year-old female production worker at a paint factory developed dermatitis on air-exposed
Hisato Ishikawa et al.
Chemical & pharmaceutical bulletin, 61(4), 438-444 (2013-04-03)
Quinoxaline derivatives having bis(fluoromethyl), bis(chloromethyl), or bis(iodomethyl) groups at the 2- and 3-positions, and various electron-donating/withdrawing substituents at the 6- and/or 7-positions, were synthesized. Their antibacterial and antifungal activities were evaluated by means of minimum inhibitory concentration assays. The relationships
Assessment and characterization of antifungal and antialgal performances for biocide-enhanced linear low-density polyethylene.
Gitchaiwat A, et al.
Journal of Applied Polymer Science, 128(1), 371-379 (2013)
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