Iodine in California Farm Milk: 1985-1986 1
John C Bruhn1, Antoine A Franke1, T Wyatt Smith1
1Departments of Food Science and Technology and Animal Science and Cooperative Extension, University of California, Davis, California 95616.
Abstract:
Iodine has been measured in 1572 California farm milk samples, representing 2,725,000 gallons of milk, or about 54% of daily production. The mean iodine concentration in the analyzed samples was 173.3 μg/kg milk, with a standard deviation of 115.8 μg/kg- The volume-corrected mean iodine concentration for all samples was 188.3 μg/kg. Of the farms examined, 13% used neither an iodine teat-dip or backflush; the milk iodine concentration on these dairy farms averaged 147.8 ± 90.2 μg/kg. Of the farms examined, 73% used iodine teat-dip only; milk iodine concentrations averaged 166.7±109.4 μg/kg. Less than 1% of the farms used iodine only in their backflush systems; their milk iodine concentrations averaged 202.3±107.2 μg/kg. Thirteen percent of the farms used both iodine teat-dip and iodine in their backflush systems; their milk iodine concentrations averaged 251.3±153.9 μg/kg. While the concentration difference between farms using iodine in both the teat-dip and backflush system and farms in the other three groups was statistically significant, the mean concentration was still well below the maximum limit of 500 μg/kg imposed by health agencies in some countries. Overall, 30.7% of samples measured has less than 100 μg iodine/kg; 70.1% had less than 200 μg/kg; 88.8% had less than 300 μg/kg; 94.4% had less than 400 μg/kg; and 98.1% had less than 500 μg/kg.
Related Concept Videos
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
SN1 Reaction: Stereochemistry
In the first step of an SN1 reaction, the bond between the electrophilic carbon and the leaving group ionizes to generate the carbocation intermediate. The second step of the mechanism is the nucleophilic attack.
In the formed carbocation, the positively charged carbon is sp2 hybridized with a trigonal planar geometry. As all the three substituents lie on the same plane, a plane of symmetry for the...
SN1 Reaction: Kinetics
However, Sir Christopher Ingold and Edward D. Hughes, who studied the kinetics of various nucleophilic substitution reactions, noticed that a tertiary alkyl halide does undergo a nucleophilic substitution reaction in the presence of a weak nucleophile. While studying the substitution...
SN1 Reaction: Mechanism
Firstly, the haloalkane ionizes to generate a carbocation intermediate and a halide ion. This heterolytic cleavage is highly endothermic with large activation energy. The ionization of the substrate, facilitated by a...
Acidity of 1-Alkynes
The acidic strength of hydrocarbons follows the order: Alkynes > Alkenes > Alkanes. The strength of an acid is commonly expressed in units of pKa — the lower the pKa, the stronger the acid. Among the hydrocarbons, terminal alkynes have lower pKa values and are, therefore, more acidic. For example, the pKa values for ethane, ethene, and acetylene are 51, 44, and 25, respectively, as shown here.
Predicting Products: SN1 vs. SN2
With increased substitution on the alkyl halide,...


