Antimicrobial oxazolidine/iodopropynyl-butyl carbamate composition containing less than 0.1wt% free formaldehyde

Abstract

This invention relates to a broad spectrum antimicrobial composition, effective against gram negative and gram positive bacteria and fungi, which comprises a synergistic composition comprising iodopropynyl butyl carbamate and a bicyclic hydroxymethyl oxazolidine containing less than 0.1% of free formaldehyde.

Description

FIELD OF THE INVENTION

[0002] The invention is primarily directed to a synergistic composition containing oxazolidine having low free formaldehyde and iodopropynyl butyl carbamate (IPBC) in a liquid glycol, water or phenoxy ethanol medium and to the preparation of the composition which is useful as a preservative in cosmetic, personal care and industrial formulations.

BACKGROUND OF THE INVENTION

[0003] Bicyclic oxazolidines are generally known and used as hardeners, corrosion inhibitors, lubricants, adhesive additives, enamel coatings and curing agents as described in U.S. Pat. Nos. 4,064,055, 4,277,353, 4,277,354, 3,982,993, 3,888,625, 3,802,897, 3,773,730, 3,725,350, 3,738,992, 3,706,950, 5,187,019, 5,684,114, 3,802,897, 3,705,832, 3,695,326, 3,281,311, 3,256,137, 3,281,310 and 3,297,611. Mixtures of bicyclic oxazolidine, used as a preservative in latex paints and emulsions, pigmented dispersions, slurries, adhesives, caulks, sealants and metal working fluids to prevent bacterial decomposition have been described in ISP BIOTREND bulletin 0040-R6, dated March 2002 One such mixture is marked under the trademark NUOSEPT 95. Also, a limited group of monocyclic oxazolidines disclosed in U.S. Pat. Nos. 4,841,064, 4,855,312 and Canadian patents 1,221,096 and 1,252,041 are defined as having biocidal properties.

[0004] Additionally, the preparation of the bicyclic compounds is set forth in technical bulletins TB 15 and TDS 40 issued by ANGUS Chemical Company and involves the condensation reaction between equimolar amounts of paraformaldehyde and an aminoalcohol. One of the challenges facing oxazolidine manufacturers and formulators using this product is the presence of free formaldehyde which has been found objectionable from human safety and environmental considerations. The stringent limits of formaldehyde in human exposure and air emissions imposed by foreign and domestic agencies, such as the Occupational Safety and Health Administration and the Environmental Protection Agency, require costly purification in the manufacture and use of formaldehyde derived oxazolidines. Additionally, in the manufacture of biheterocyclic compounds such as oxymethylene oxazolidine, it is desirable to minimize or eliminate the formation of alkoxylated derivatives which significantly reduce its activity and stability.

[0005] IPBC has been independently described as a biocide for certain algae in U.S. Pat. No. 6,121,198. However, this carbamate exhibits mostly antifungal efficacy against several other species.

[0006] Accordingly, it is an object of this invention to provide a broad spectrum antimicrobial liquid composition which has less than 0.1 wt. % of free formaldehyde.

[0007] Another object is to provide a liquid biocidal oxazolidine composition which is non-toxic to humans and safe for incorporation in topical personal care formulations.

[0008] Another object of the invention is to provide a commercially feasible and economical process for producing a bicyclic oxazolidine and IPBC mixture containing low levels of free formaldehyde.

[0009] Still another object is to prepare a synergistic mixture of biocides which is effective against gram negative and gram positive bacteria as well as fungi.

[0010] Still another object is to provide a clear liquid composition containing a mixture of oxazolidine and IPBC which is resistant to precipitation or crystallization and which is substantially colorless.

[0011] These and other objects and advantages of the invention will become apparent from the following description and disclosure.

SUMMARY OF THE INVENTION

[0012] In accordance with the present invention, there is provided (a) a clear aqueous glycol solution of a synergistic antimicrobial hydroxymethyl bicyclic oxazolidine (HMBO)/IPBC composition which contains less than 0.1 wt. % of free formaldehyde and other functional group substitutions and (b) a process for making the composition which requires reacting a glycol slurry of paraformaldehyde with a controlled critical molar amount of tris(hydroxymethyl)-aminomethane before addition of a predetermined amount of IPBC.

DETAILED DESCRIPTION OF THE INVENTION

[0013] The present invention is directed to a synergistic, biocidal composition that is non-toxic to humans and the environment under normal conditions of exposure and is suitable for controlling harmful bacteria and fungi which comprises a 1.0-60 wt. % glycol solution containing, as the active components, a mixture of between 20 and 60 wt. % of said aliphatic, hydroxymethyl bicyclic oxazolidine (HMBO), particularly the bicyclic hydroxymethyl oxazolidine, and between 0.01 and 10 wt. % IPBC. In the composition, bicyclic hydroxymethyl oxazolidine is preferred and optionally may contain up to 5 wt. % of another aliphatic oxazolidine biocide as in a blend or admixture. However, synergistic biocidal properties between hydroxymethyl oxazolidine and IPBC have been discovered.

[0014] This synergistic composition is prepared by a process which demands observance of certain critical parameters. More specifically, for the preparation of the bicyclic hydroxymethyl oxazolidine (HMBO)/IPBC composition, paraformaldehyde as a uniform slurry in a glycol reaction medium is reacted with a critical 0.75-5.3% molar excess, preferably a 1-5% molar excess, of tris(hydroxymethyl)aminomethane at a temperature between about 35 and about 60° C. for a period of from 1 to 5 hours to yield at least 99.9% pure bicyclic oxazolidine product and 2 moles of water by-product. The reaction medium is mixed until a clear solution is formed, insuring that all of the formaldehyde has reacted. The tris(hydroxymethyl)aminomethane co-reactant is added in portions throughout the reaction and continuously mixed to retain clarity in the production of the present product containing less than 0.1 wt. % free formaldehyde and other minor by-products.

[0015] The clear solution of the oxazolidine product, containing between about 1.0 and 60 wt. % glycols and between about 12 and about 15 wt. % water, is subsequently contacted at ambient or up to 50° C. elevated temperature with between about 0.1 and about 10 wt. %, preferably 0.1-5 wt. %, of IPBC which is added under agitation throughout a period of from about 1 to about 2.5 hours. The clear liquid composition thus produced exhibits broad spectrum biocidal properties effective against gram negative and gram positive bacteria as well as fungi which composition exhibits biocidal properties greater than the sum of those achievable with the individual components.

[0016] The liquid medium suitable for the condensation reaction and subsequent combination with IPBC is an aliphatic polyhydroxy compound such as a C3 to C6 diol or other liquid glycol, including propylene glycol, dipropylene glycol, tripropylene glycol, glycol triols, 1,4- and 1,3-dihydroxy butanes and ethoxylated and/or propoxylated derivatives phenoxy ethanol thereof or mixtures of these. Preferred of this group are polyethylene glycol-PEG 400, butanediol and phenoxyethanol.

[0017] The paraformaldehyde slurry introduced into the reactor is desirably a 45 to 75% glycol or phenoxy ethanol suspension which is continuously agitated during the reaction and gradually heated to reaction temperature. Since the paraformaldehyde and the tris(hydroxymethyl) aminomethane (THAM) are both of low solubility in the liquid medium, completion of the condensation reaction and depletion of the formaldehyde is indicated by the formation of a clear solution of soluble bicyclic oxazolidine.

[0018] The most preferred reaction conditions include maintaining the molar excess of the tris(hydroxymethyl)aminomethane between 1.1 and 3% until two moles of water by-product are formed and effecting the reaction over a period of from 3-4 hours at a temperature of 50-60° C.

[0019] The basic reaction forming the bicyclic hydroxymethyl oxazolidine is defined by the equation: 1

[0020] As pointed out above the present broad spectrum biocidal composition is particularly suitable for personal care formulations in a concentration of up to 5 wt. %, preferably 0.02-1.0% concentration, to prevent deterioration and extended shelf life of the product.

[0021] Also, the present composition is suitably employed in 0.02 to 1.0% concentrations to minimize degradation of industrial products such as paints, coatings, adhesives, sealants, caulks and the like. The following illustrate a few typical examples of suitable formulations to which the present preservative is beneficially added.

[0022] Some formulations which beneficially employ the product of this invention are presented in the following disclosure.

[0023] Having generally described the invention, reference is now had to the following examples which illustrate preferred embodiments but are not to be construed as limiting to the scope of the invention as set forth in the accompanying claims.

EXAMPLE 1

Preparation of Hydroxymethyl Oxazolidine/Iodopropynyl Butylcarbamate Biocidal Composition

[0024] A closed vessel is charged with 102 g of 1,3-dihydroxybutane and 62 g of prilled paraformaldehyde is added and mixed at room temperature until a uniform slurry is formed. The slurry is then heated to 60° C. and a 2% molar (or 1-5%) molar excess of tris(hydroxymethyl)aminomethane (THAM) is introduced. A total of 124 g of 99% pure tris(hydroxymethyl)aminomethane is gradually added in increasing increments until a 2% molar excess is obtained. The ensuing condensation reaction takes place over a period of 3 hours. During the reaction, soluble bicyclic hydroxymethyl oxazolidine is continuously formed. Since paraformaldehyde and tris(hydroxymethyl)-aminomethane are of low solubility in the reaction medium, completion of the reaction is indicated when a clear solution is formed with water by-product. When the mixture becomes clear, insuring that all of the formaldehyde has reacted, the resulting solution is allowed to cool to ambient temperature and 4.42 g of powdered IPBC (weight ratio of bicyclic hydroxymethyl oxazolidine HMBO to IPBC is 33:1) is added and stirred until a clear solution is obtained. No crystallization of IPBC is noted in the substantially colorless product and a pure clear, liquid composition containing less than 1000 ppm of formaldehyde is obtained.

EXAMPLES 2-16

[0025] The above general procedure described in Example 1 was repeated in Examples 2-8, except that the weight ratio of HMBO to IPBC and reaction media were varied as noted in the following Table 1.

TABLE 1
		Wt. ratio
Ex.	Reaction media	HMBO:IPBC	Description of Composition
2	propylene glycol	17:1	Clear
3	propylene glycol	10:1	Slight crystallization occurs
4	1,3-butanediol	100:1	Clear
5	1,3-butanediol	33:1	Clear
6	1,3-butanediol	17:1	Clear
7	1,3-butanediol	10:1	Clear
8	dipropylene glycol	17:1	Clear
9	dipropylene glycol	10:1	Clear
10	PEG-400	100:1	Clear
11	PEG-400	33:1	Clear
12	PEG-400	17:1	Clear
13	PEG-400	10:1	Clear
14	phenoxyethanol	100:1	Clear
15	phenoxyethanol	33:1	Clear
16	phenoxyethanol	17:1	Clear

[0026] The present biocidal compositions Examples 1-3, 4, 8, 12, 13, 5, 6, 9, 10, 11 were evaluated for efficacy against:

[0027] A. Candida albicans 10231 yeast, (CAN)

[0028] B. Staphylococcus aureus 6538 bacteria, (SA)

[0029] C. Pseudomonas aeruginosa 9027, (PSA)

[0030] D. Burkholderia cepacia 25416, (BC)

[0031] E. Escherichia coli 8739 and (EC)

[0032] F. Aspergillus niger 16404 (mold) (AN)

[0033] employed in the following antimicrobial evaluations as reported in Table 2.

[0034] In the following tests, 1:2 molar ratio of tris(hydroxymethyl)-aminomethane to formaldehyde was used with 0.5% and 1.5% IPBC in emulsions I. or II. reported below.

I. Standard Screening Emulsion	II. Non-ionic Screening Emulsion
Stearic acid	5 wt. %	Water (distilled)	70.1 wt. %
Mineral oil	2.5 wt. %	Stabileze QM*	0.20 wt. %
Cetyl alcohol	1.0 wt. %	2-ethyl hexylpalmitate	10.0 wt. %
Ceteareth 5****	0.5 wt. %	Mix of cetyl & stearyl	2.0 wt. %
		alcohols
Glyceryl	1.5 wt. %	Ceteareth-20**	2.0 wt. %
Monostearate/
PEG 100Stearate
Water	87.90 wt. %	Glyceryl stearate	0.5 wt. %
Triethanolamine	1.0 wt. %	Laureth-23***	2.50 wt. %
Citric acid, 30% aq.	0.6 wt. %	Isocetylstearate	10 wt. %
		Triethanolamine	0.2 wt. %
*decadiene crosslinked methyl vinyl ether/Maleic anhydride copolymer
**mixture of C16 & C18 (ethoxy)20 alcohols
***polyoxyethylene(23) lauryl ether & mixture of C16 & C18 (ethoxy)5 alcohols
****polyethyleneglycol of cetearyl alcohol

[0035]

TABLE 2
HMBO/1.5% or 3.0% IPBC in phenoxyethanol
SCREENING EMULSION
Preservative	ppm acitves	Organism	48 hrs	7 days	14 days	21 days	28 days
49.3% HMBO/	493 ppm	SA	70,000	<10	<10	<10	<10
1.5% IPBC/	15 ppm	EC	50	<10	<10	<10	<10
phenoxyethanol		PSA	<10	<10	<10	<10	<10
Use level - 0.1%		BC	<10	<10	<10	<10	<10
		CAN	4,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
49.3% HMBO/	986 ppm	SA	34,000	<10	<10	<10	<10
1.5% IPBC/	30 ppm	EC	20	<10	<10	<10	<10
phenoxyethanol		PSA	<10	<10	<10	<10	<10
use level - 0.2%		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
48.5% HMBO/	485 ppm	SA	15,000	<10	<10	<10	<10
3.0% IPBC/	30 ppm	EC	<10	<10	<10	<10	<10
phenoxyethanol		PSA	<10	<10	<10	<10	<10
use level - 0.1%		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
48.5% HMBO/	970 ppm	SA	<10	<10	<10	<10	<10
3.0% IPBC/	60 ppm	EC	<10	<10	<10	<10	<10
phenoxyethanol		PSA	<10	<10	<10	<10	<10
use level - 0.2%		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	390,000	4.50E+03	2.10E+02	>1E4
		EC	>1E6	860	>1E4	>1E4	>1E4
		PSA	>1E6	790	>1E4	>1E4	>1E4
		BC	>1E6	>1E6	>1E4	>1E4	>1E4
		CAN	>1E6	>1E6	>1E6	>1E6	>1E6
		AN	>1E6	>1E6	>1E4	>1E4	>1E4

[0036] In repetitions of the above evaluations, there was significant reduction of the organisms after 48 hours for all solvent systems at a 0.2% emulsion dosage level.

EXAMPLE 17

[0037] MIC Data on Microbiological Media

[0038] To demonstrate synergism in microbiological growth media a wide range of concentrations and ratios of compounds, generated by serial dilutions were added into Tryptic Soy Broth (TSB) for bacterial evaluations or to Malt Agar (M) for fungal evaluations. Antimicrobial activity was demonstrated against the bacterium Bacillus subtilis (ATCC 27328) or the fungi Aureobasidium pullulans (ATCC 9348) and Aspergillus niger (ATCC 6275). One hundred μl of the bacterial suspensions were added to TSB broth containing each biocide or biocide mixture to a final concentration of approximately 106 CFU/ml. The inoculated broth was then incubated at 32° C. for 2-3 days. For fungi MIC, 10 μl of the fungi suspensions were pipetted to the solidified Malt agar containing various concentrations of each biocide or the biocide mixture. Final concentration about 105 spores/ml. Plates were incubated for 10-12 days at 28° C.

[0039] The lowest concentration of each compound or mixture to inhibit visible growth at 32° C. after 2-3 days for bacteria and at 28° after 10-12 days for fungi were taken as the Minimal Inhibitory Concentration (MIC). The MIC was taken as endpoints of activity. End points for the mixture of HMBO and IPBC where then compared with the end points for the pure active compound when employed individually.

[0040] Synergism was determined by a commonly used method described by Kull, A. C., Eisman, P. C, Sylwestrowicz, H., D. and Mayer, R. L. (1961). Applied Microbiology, 9:538 using the ratio determined by: Qa/QA+Qb/QB=Synergy Index (SI).

[0041] Wherein: QA is the concentration of HMBO in parts per million (ppm), acting alone, which produced and end point. Qa is the concentration of HMBO in ppm, in the mixture, which produced and end point. QB is the concentration of IPBC in ppm, acting alone, which produced an end point and Qb is the concentraton of IPBC in ppm, in the mixture, which produced an end point.

[0042] When the sum of Qa/QA+Qb/QB is greater than one, antagonism is indicated. When the sum is equal to one, additivity is indicated. When the sum is less than one, synergism is demonstrated.

[0043] The results, which serve to demonstrate the synergism of this biocidal combination in microbiological media are compiled in Table 3 as shown below, wherein compound A is HMBO containing less than 0.1 wt. % formaldehyde and compound B is IPBC.

TABLE 3
Low free formaldehyde HMBO (compound A)/
IPBC(compound B)
	A	B
Microorganism	(ppm)	(ppm)	A:B	Synergy Index
Bacillus subtilis	250	0
	62.5	31.2	2:1	0.75
	0	62.5
Aspergillus niger	1,000	0
	50	0.1	500:1	0.45
	100	0.1	1,000:1	0.50
	500	0.1	5,000:1	0.90
	250	0.05	5,000:1	0.45
	500	0.05	10,000:1	0.70
	0	0.25
Alternaria alternata	250	0
	100	0.25	400:1	0.70
	250	0.10	2,500	0.70
	0	0.50

EXAMPLE 18

[0044] The efficacy of each individual compound or their combination was measured in a latex paint artificially contaminated with a mixed inoculum. The microbiological evaluations shown as examples, are based on ASTM D2574-94, “Resistance of emulsion paints in the container to the attack of microorganisms”. Briefly, paint samples (e.g. Polyvinyl Acrylic, PCL 717) were prepared to contain different concentrations of each compound or their mixtures in different concentrations and ratios. Each paint sample thus prepared was then inoculated with a mixed culture of Pseudomonas aeruginosa, Enterobacter cloacae, Bacillus subtilis, B. megaterium, B. licheniformis, Aspergillus niger and Penicillium funiculosum (final concentration of about 106 CFU/ml) and re-challenged after 7 days (final concentration of about 107 CFU/ml). Paint samples were incubated at 32° C. for the duration of the test and sampled for the presence of viable bacteria on TSA and M plates. Growth was rated on a scale from “0” (no growth) to “4” (heavy growth). A paint sample was considered appropriately preserved if no bacterial growth (“0” rating) was detected after six days incubation in both challenge assays.

[0045] Table 4 shows the synergistic effects of the compounds when tested in a typical polyvinyl acrylic paint. The table summarizes the results obtained when mixtures of the low formaldehyde hydroxymethyl oxazolidine (HMBO) (compound A) and IPBC (compound B) in PEG-400 were tested.

TABLE 4
Ratio	Total	TSA plates	MALT Plates
Actives	Actives	CI	CII	CI	CII
(A:B)	PPM	1	2	3	6	1	2	3	6	1	2	3	6	1	2	3	6
25:1	380	1	0	0	0	1	0	0	0	1	0	0	0	0	0	1	0
	(365:15)
17:1	545	0	0	1	0	1	1	0	0	0	0	0	0	1	1	0	0
	(515:30)
A alone	500	0	0	0	0	1	1	1	1	0	0	0	0	0	0	0	0
	520	0	0	0	0	0	0	1	0	0	0	0	0	0	1	1	0
B alone	60	0	0	1	0	4	4	4	3	0	1	0	0	4	4	4	4
	120	4	2	0	0	4	3	3	3	4	4	2	0	4	4	4	4
	200	4	2	0	0	4	3	3	3	4	2	1	0	4	4	4	4
Control	—	1	0	0	0	4	4	4	3	0	1	0	0	4	4	4	4

[0046] The present low formaldehyde HMBO/IPBC emulsion was tested with various organisms in different solvents. The results of these tests is reported in following Tables 5-11.

TABLE 5
48.5% HMBO/3% IPBC in different solvent systems
SCREENING EMULSION
Preservative	ppm active	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/3% IPBC	485 HMBO	SA	270	<10	<10	<10	<10
in propylene	30 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	485 HMBO	SA	70	<10	<10	<10	<10
dipropylene	30 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	485 HMBO	SA	20	<10	<10	<10	<10
polyethylene	30 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	485 HMBO	SA	<10	<10	<10	<10	<10
1,3 butanediol	30 IPBC	EC	<10	<10	<10	<10	<10
0.1% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	17,000	70	60	>1E4
		EC	61,000	249,000	>1E4	>1E4	>1E4
		PSA	8,000	1.00E+04	>1E4	>1E4	>1E4
		BC	>1E6	>1E6	>1E4	>1E4	>1E4
		CAN	600,000	580,000	>1E4	>1E4	>1E4
		AN	75,000	140,000	>1E4	>1E4	>1E4

[0047]

TABLE 6
47.5% HMBO/5% IPBC in different solvent systems
SCREENING EMULSION
Preservative	ppm actives	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/5% IPBC	475 HMBO	SA	240	<10	<10	<10	<10
in propylene	50 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	475 HMBO	SA	100	<10	<10	<10	<10
dipropylene	50 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	475 HMBO	SA	<10	<10	<10	<10	<10
polyethylene	50 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.1% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	475 HMBO	SA	<10	<10	<10	<10	<10
1,3 butanediol	50 IPBC	EC	<10	<10	<10	<10	<10
0.1% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	17,000	70	60	>1E4
		EC	61,000	249,000	>1E4	>1E4	>1E4
		PSA	8,000	1.00E+04	>1E4	>1E4	>1E4
		BC	>1E6	>1E6	>1E4	>1E4	>1E4
		CAN	600,000	580,000	>1E4	>1E4	>1E4
		AN	75,000	140,000	>1E4	>1E4	>1E4

[0048]

TABLE 7
48.5% HMBO/3% IPBC in different solvent systems
SCREENING EMULSION
Preservative	Use Level	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
in propylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
dipropylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
polyethylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
1,3 butanediol	120 IPBC	EC	<10	<10	<10	<10	<10
0.4% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	17,000	7.00E+01	6.00E+01	>1E4
		EC	61,000	249,000	>1E4	>1E4	>1E4
		PSA	8,000	10,000	>1E4	>1E4	>1E4
		BC	>1E6	>1E6	>1E4	>1E4	>1E4
		CAN	600,000	5.80E+05	>1E4	>1E4	>1E4
		AN	75,000	140,000	>1E4	>1E4	>1E4

[0049]

TABLE 8
47.5% HMBO/5% IPBC in different solvent systems
SCREENING EMULSION
Preservative	ppm actives	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/5% IPBC	1900 HMBO	SA	<10	<10	<10	<10	<10
in propylene	200 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	1900 HMBO	SA	<10	<10	<10	<10	<10
dipropylene	200 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	1900 HMBO	SA	<10	<10	<10	<10	<10
polyethylene	200 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/5% IPBC	1900 HMBO	SA	<10	<10	<10	<10	<10
1,3 butanediol	200 IPBC	EC	<10	<10	<10	<10	<10
0.4% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	17,000	7.00E+01	6.00E+01	>1E4
		EC	61,000	249,000	>1E4	>1E4	>1E4
		PSA	8,000	10,000	>1E4	>1E4	>1E4
		BC	>1E6	>1E6	>1E4	>1E4	>1E4
		CAN	600,000	5.80E+05	>1E4	>1E4	>1E4
		AN	75,000	140,000	>1E4	>1E4	>1E4

[0050]

TABLE 9
48.5% HMBO/3% IPBC in different solvent systems
NONIONIC EMULSION BASE
Preservative	ppm actives	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/3% IPBC	970 HMBO	SA	<10	<10	<10	<10	<10
in propylene	60 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.2% use level		BC	<10	<10	<10	<10	<10
		CAN	20,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	970 HMBO	SA	<10	<10	<10	<10	<10
dipropylene	60 IPBC	EC	6.60E+02	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.2% use level		BC	<10	<10	<10	<10	<10
		CAN	33,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	970 HMBO	SA	<10	<10	<10	<10	<10
polyethylene	60 IPBC	EC	90	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.2% use level		BC	<10	<10	<10	<10	<10
		CAN	13,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	970 HMBO	SA	10	<10	<10	<10	<10
1,3 butanediol	60 IPBC	EC	<10	<10	<10	<10	<10
0.2% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	30,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	>1E4	7.60E+03	4.00E+01	>1E4
		EC	>1E6	>1E4	>1E4	>1E4	>1E4
		PSA	>1E6	>1E4	>1E4	>1E4	>1E4
		BC	>1E6	>1E4	>1E4	>1E4	>1E4
		CAN	>1E6	>1E4	>1E4	>1E4	>1E4
		AN	320,000	>1E4	>1E4	>1E4	>1E4

[0051]

TABLE 10
48.5% HMBO/3% IPBC in different solvent systems
NONIONIC EMULSION
Preservative	ppm actives	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
in propylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	900	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
dipropylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	3,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
polyethylene	120 IPBC	EC	<10	<10	<10	<10	<10
glycol		PSA	<10	<10	<10	<10	<10
0.4% use level		BC	<10	<10	<10	<10	<10
		CAN	2,000	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/3% IPBC	1940 HMBO	SA	<10	<10	<10	<10	<10
1,3 butanediol	120 IPBC	EC	<10	<10	<10	<10	<10
0.4% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	960	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
unpreserved		SA	>1E6	>1E4	7.60E+03	4.00E+01	>1E4
		EC	>1E6	>1E4	>1E4	>1E4	>1E4
		PSA	>1E6	>1E4	>1E4	>1E4	>1E4
		BC	>1E6	>1E4	>1E4	>1E4	>1E4
		CAN	>1E6	>1E4	>1E4	>1E4	>1E4
		AN	320,000	>1E4	>1E4	>1E4	>1E4

[0052]

TABLE 11
49.3% HMBO/1.5% IPBC in 1,3 butanediol
SCREENING EMULSION
Preservative	ppm acitves	Organism	48 hrs	7 days	14 days	21 days	28 days
HMBO/1.5% IPBC	986 HMBO	SA	410	<10	<10	<10	<10
1,3 butanediol	30 IPBC	EC	<10	<10	<10	<10	<10
0.2% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	<10	<10	<10	<10	<10
		AN	<10	<10	<10	<10	<10
HMBO/1.5% O{BC	493 HMBO	SA	9,000	<10	<10	<10	<10
1,3 butanediol	15 IPBC	EC	<10	<10	<10	<10	<10
0.1% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	460	<10	<10	<10	<10
		AN	20	<10	<10	<10	<10
HMBO/1.5% IPBC	247 HMBO	SA	4,100,000	<10	<10	<10	<10
1,3 butanediol	7.5 IPBC	EC	1,000	<10	<10	<10	<10
.05% use level		PSA	<10	<10	<10	<10	<10
		BC	<10	<10	<10	<10	<10
		CAN	170,000	<10	<10	<10	<10
		AN	50	<10	<10	<10	<10
unpreserved		SA	>1E6	>1E4	>1E4	>1E4	>1E4
		EC	600,000	>1E4	>1E4	>1E4	>1E4
		PSA	>1E6	>1E4	>1E4	>1E4	>1E4
		BC	>1E6	>1E4	>1E4	>1E4	>1E4
		CAN	>1E6	360,000	>1E4	>1E4	>1E4
		AN	>1E6	220,000	>1E4	>1E4	>1E4

Claims

1. A broad spectrum, synergistic biocidal composition comprising a mixture of a biocidal cyclic hydroxymethyl oxazolidine containing less than 0.1 wt. % free formaldehyde and between about 0.1 and about 10 wt. % of iodopropynyl butylcarbamate in an aqueous solution of a polyhydroxide of a C3 to C6 aliphatic hydrocarbon, a phenoxyethanol or a mixture thereof.

2. The composition of claim 1 wherein said solution is an aqueous solution of a compound selected from the group consisting of a C3 to C6 diol, phenoxyethanol optionally alkoxylated with a C2 to C3 alkoxyl group, polyethylene glycol and mixtures thereof.

3. The composition of claim 2 wherein said solution is an aqueous solution of butanediol, phenoxyethanol or a mixture thereof.

4. The composition of claim 1 wherein said cyclic hydroxymethyl oxazolidine is bicyclic hydroxymethyl oxazolidine.

5. The composition of one of claims 1, 2 or 3 wherein the composition contains between 0.1 and 5 wt. % of iodopropynyl butylcarbamate.

6. The composition of one of claims 1, 2, 3 or 4 wherein the weight ratio of hydroxymethyl oxazolidine to iodopropynyl butyl carbamate is between about 10:1 and about 100:1.

7. The process of preparing the composition of claim 1 which comprises: (a) forming a uniform slurry of paraformaldehyde in a liquid selected from the group consisting of an aqueous solujtion of a polyhydroxide of a C3 to C6 hydrocarbon, phenoxyethanol, ethoxylated or propoxylated phenoxyethanol, polyethylene glycol, polypropylene glycol or a mixture thereof; (b) heating the slurry to a temperature of from about 35 to about 60° C.; (c) introducing a 0.75 to 5 molar excess of tris(hydroxymethyl)-aminomethane into said slurry; (d) agitating the mixture of (c) while constantly maintaining said excess of tris(hydroxymethyl)aminomethane until completion of the reaction indicated by the formation of the substantially pure cyclic hydroxymethyl oxazolidine in a clear solution; (e) adding between about 0.1 and about 10 wt. % of iodopropynyl butylcarbamate, based on said oxazolidine, to the product of step (d); (f) constantly agitating the contents of (e) until a second clear solution is formed and recovering the solution of (f) as the solution of composition of iodopropynyl butylcarbamate/cyclic hydroxymethyl oxazolidine containing less than 0.1 wt. % free formaldehyde.

8. The process of claim 7 wherein said aqueous solution in step (a) is butanediol or phenoxyethanol or a mixture thereof.

9. A personal care formulation containing 0.05 to 1.0 wt. % biocidal amount of the composition of one of claims 1, 2, 3 or 4.

10. A personal care formulation containing a biocidal amount between 0.05 and 1.0 wt. % of the composition of claim 1.

11. The personal care formulation of claim 10 selected from the group consisting of a hair spray, hair dye, skin lotion and hair conditioner.

12. An industrial formulation selected from the group of a paint, adhesive, ink, pigment dispersion or slurry, paper pulp mixture, latex emulsion, metalworking fluid, caulk and sealant containing between about 0.05-1.0 wt. % of the composition of one of claims 1, 2, 3 or 4.