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Postharvest Biology and Technology of Fruits, Vegetables, and Flowers

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140 POSTHARVEST BIOLOGY & TECHNOLOGY OF FRUITS, VEGETABLES, & FLOWERS<br />

CH 3<br />

Fig. 7.1<br />

Structure <strong>of</strong> 1-MCP.<br />

7.2 Registration <strong>and</strong> application <strong>of</strong> 1-MCP<br />

Commercial applications <strong>of</strong> 1-MCP were first made available for ornamental crops. This<br />

product with the trade name EthylBloc was approved by the United States Environmental<br />

Protection Agency (EPA) in 1999, <strong>and</strong> was marketed by Floralife, Inc. (Waterboro, SC).<br />

Further testing <strong>and</strong> registration <strong>of</strong> 1-MCP for edible crops were undertaken by AgroFresh<br />

Inc., a subsidiary <strong>of</strong> Rohm <strong>and</strong> Haas (Springhouse, PA). Several investigations have shown<br />

that 1-MCP is nontoxic to humans, has negligible residue, <strong>and</strong> is active at concentrations<br />

<strong>of</strong> parts per billion (ppb).<br />

The safety, toxicity, <strong>and</strong> environmental pr<strong>of</strong>iles <strong>of</strong> 1-MCP to humans, animals, <strong>and</strong> in<br />

the environment were reported by the EPA (2002). The LC 50 for inhalation in rats was<br />

greater than 2.5 mg/L (or 1,126 ppm active ingredient in air). Acute toxicity <strong>of</strong> 1-MCP or<br />

clinical signs <strong>of</strong> systemic toxicology have not been observed in toxicology studies (EPA,<br />

2002).<br />

With the approval by the EPA in 2002, 1-MCP is marketed under the trade name <strong>of</strong><br />

SmartFresh. The use <strong>of</strong> SmartFresh has been approved by over 20 countries. The approval is<br />

for specific crops <strong>and</strong> includes apple, apricot, avocado, carrot, kiwifruit, mango, melon, nectarine,<br />

papaya, peach, pear, pepper, persimmon, pineapple, plantain, plum, squash, tomato,<br />

<strong>and</strong> tulip bulbs. Table 7.1 gives a summary <strong>of</strong> the fruits <strong>and</strong> vegetables that respond to 1-MCP.<br />

At 20 ◦ C, 1-MCP is released as a gas from a formulated cyclodextrin powder when it<br />

is mixed with water in nearly 20–30 min. A complete release may take longer duration at<br />

lower temperatures. Under such conditions, 1-MCP is absorbed by the harvested material<br />

over time. Peaches absorbed 80–90% <strong>of</strong> the 1 μL/L applied either at 20 ◦ Cor0 ◦ C when held<br />

in a closed container for 20 h (Liguori et al., 2004). As well, an increase in CO 2 levels due to<br />

respiration does not inhibit the effectiveness <strong>of</strong> binding <strong>of</strong> 1-MCP (Blankenship <strong>and</strong> Dole,<br />

2003) in closed systems. In addition, ethylene is also produced by harvested materials. Since<br />

1-MCP shows a higher affinity toward the ethylene receptor, nearly 100-fold higher levels <strong>of</strong><br />

ethylene are required to effectively compete for the binding site. The highest concentration<br />

<strong>of</strong> 1-MCP that is approved for use is 1 μL/L. After binding to the receptors, 1-MCP does not<br />

get released, <strong>and</strong> any reversal <strong>of</strong> 1-MCP treatment is potentially because <strong>of</strong> the synthesis<br />

<strong>of</strong> new ethylene receptors in the tissue (E.C. Sisler, personal communication). Repeated<br />

weekly applications <strong>of</strong> 1-MCP (Mir et al., 2001; Mir <strong>and</strong> Beaudry, 2001; Jayanty et al.,<br />

2004) helped prevent apple s<strong>of</strong>tening at 20 ◦ C more than at 0 ◦ C, <strong>and</strong> this was attributed to<br />

an increased turnover <strong>of</strong> the receptor at high storage temperature.<br />

It has also been noticed that 1-MCP can be absorbed or adsorbed nonspecifically to<br />

sites other than ethylene receptors. In storage rooms, various plastics did not absorb the

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