Nalgene

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Two Nalgene wash bottles featuring the NFPA 704 color code for hazardous materials identification Nalgene bottles.jpg
Two Nalgene wash bottles featuring the NFPA 704 color code for hazardous materials identification

Nalgene is a brand of plastic products developed originally for laboratory use, including items such as jars, bottles, test tubes, and Petri dishes, that were shatterproof and lighter than glass. The properties of plastic products make them suitable for work with many substances in various temperature ranges.

Contents

Nalgene products are manufactured by Nalge Nunc International, which in 2004 became a subsidiary of Fisher Scientific, now Thermo Fisher Scientific. [1] The name Nalgene is a registered trademark.

Nalgene Outdoor

Narrow-mouth Nalgene bottle with custom attachment point Nalgene edited.jpg
Narrow-mouth Nalgene bottle with custom attachment point

In the 1970s, conservationists began discouraging the disposal of cans and glass bottles by burning and burial in wilderness and recreation areas, and some places began forbidding such materials by regulation. Nalgene products became popular replacements among backpackers for storing consumables; the light, wide-mouthed high-density polyethylene (HDPE) and polycarbonate bottles were more secure than plastic bags and were used for both liquids and solid foods.

Originally, wilderness travelers purchased Nalgene products from laboratory-equipment suppliers, or perhaps gained access to them in their workplaces. Company lore has it that Nalge Company president Marsh Hyman, based in Rochester, NY, discovered that his son's Boy Scout troop was using Nalgene laboratory containers when camping. Since then, the company has re-packaged and marketed items for consumer sales through their line of Nalgene Outdoor products. [2] By the late 1990s, the "Nalgene" trademark was recognized by many hikers, and sales of the 1-litre wide-mouth bottle of translucent polycarbonate (originally typically grey, but now commonly in bright colors, often with custom labels made for the bottle retailer) with a screw-on plastic top that stays attached when the bottle is open, began to increase. Today, many hikers and others recognize the distinctive appearance of Nalgene-branded bottles. Its laboratory pedigree is still suggested by the markings, in hundreds of millilitres, of the volume contained. The materials resist stains and odor absorption, and can be filled with boiling water. [3] The wide-mouth bottle is more widely used and sold over the narrow-mouth bottles in sub-freezing conditions, since it is easier to break through ice with the wider mouth.[ citation needed ] Currently, Nalgene markets over twelve different sizes of bottles in many colours, including the classic Wide Mouth and Narrow Mouth. [4]

Wide-mouth 1-litre bottle Blue 1000 ml Nalgene everyday wide mouth bottle 2.JPG
Wide-mouth 1-litre bottle

A variety of products from other manufacturers are designed for compatibility with this item's overall dimensions or its 2.5-inch neck; these include:

Another widely available Nalgene Outdoor product is a 650 ml (22 fl oz) "All-Terrain" or "bike" bottle. The bottle is made from low-density polyethylene (LDPE), and its screw top has two moving parts — a drinking nozzle that seals until snapped open by pulling on it, and a hinged polycarbonate dome, that when closed both snaps the nozzle closed and protects the nozzle against contamination. Unlike traditional Nalgene containers, this item can be damaged and potentially ruined by filling it with very hot water.

Recently, Nalgene has added hydration systems to its cycling and wilderness product line. The line features 1- to 3-litre bladders with hose-and-bite-valve assemblies in small back-carried packs (mostly under 1000 cubic inches, or 16 L, of additional storage). Nalgene offers the option of two different bladder materials for a choice of superior taste and bacteria resistance versus improved durability. In addition, the bladder on these products can be quickly detached from the hose and pack by a self-sealing connector on the bladder. These features were intended to improve on perceived issues with existing hydration systems, including difficulty filling and/or leaking water into gear that shares the pack.

Increased awareness of the importance of hydration while exercising has led to the appearance of some Nalgene containers in urban and suburban settings like gyms, offices, and campuses. Many colleges give or sell Nalgene water bottles to their students, and Nalgene bottles are also customized and sold as retail promotions.

In October 2017, Nalgene launched a new line of colors for their water bottles. [5]

Bisphenol A (BPA) concerns

In recent years, studies have suggested that polycarbonates, made from bisphenol A (BPA) and phosgene (COCl
2
), such as the ones Nalgene used, may leach endocrine disruptors including BPA. [6] Nalgene denies that the quantity leached from their products posed a significant threat to health. [6] Among the secreted chemicals, BPA is a concern, as it binds to estrogen receptors, thus altering gene expression. [7] [8] [9] Other research has found that fixatives[ clarification needed ] in polycarbonate plastics can cause chromosomal error in cell division called aneuploidy. Nalgene claims these chemicals are only potentially released from Nalgene products when used at temperatures outside of the designed range. [10]

In November 2007, the national Canadian co-operative retailer Mountain Equipment Co-op removed all hard, clear polycarbonate plastic water bottles (including Nalgene-branded products) from their shelves and replaced them with BPA-free Nalgene bottles. In December 2007, Lululemon made a similar move. In May 2008, Recreational Equipment, Inc. removed Nalgene-branded polycarbonate water bottles and replaced them with BPA-free Nalgene bottles.

On April 18, 2008, Health Canada announced that bisphenol A is "'toxic' to human health". [11] On the same date, Nalgene announced it would phase out production of its Outdoor line of polycarbonate containers containing BPA. [12] Nalgene subsequently adopted Tritan copolyester, a BPA-free copolyester made by Eastman Chemical, as a substitute. [13]

Although unpublished studies in 2008 and 2009 by Oregon State students suggest that BPA does not leach from polycarbonate plastic under extreme conditions, BPA is not the only component of plastics which can mimic estrogen and act as an endocrine disruptor. [14] Unfortunately, BPA-free Tritan plastics were later found to leach other estrogenic chemicals in a cell-based assay. [15] Eastman Chemical, the manufacturer of Tritan, will not disclose precise information about the chemical structure of Tritan. [16]

A study from CertiChem (a private lab in Austin, Texas dedicated to studying endocrine disruption) found that green-colored Nalgene bottles effectively block the effects of UV rays, thus rendering the specific model studied safe from specific BPA-leaching concerns. However, CertiChem's founder and neuroscience professor at the University of Texas at Austin, George Bittner, cautioned that green Nalgene bottles found in stores "aren't guaranteed to be safe since minor change to the chemical formula can introduce estrogens". [17] Bitter also published an article claiming most polymers, including Tritan, contained trace amounts of Bisphenol A. [15] Eastman Chemical Company filed a lawsuit after these results were publicized in a brochure produced by PlastiPure, a sister company to CertiChem. Eastman maintained that the tests used by CertiChem, which were based around cultured estrogen-sensitive breast cancer cells, were not a definitive assay of endocrine activity in vivo. A jury ruled in Eastman's favor, and as a result Bittner, PlastiPure, and CertiChem were barred from making claims about Tritan’s oestrogenic activity. [18]

See also

Related Research Articles

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<span class="mw-page-title-main">Phthalates</span> Any ester derived from phthalic acid

Phthalates, or phthalate esters, are esters of phthalic acid. They are mainly used as plasticizers, i.e., substances added to plastics to increase their flexibility, transparency, durability, and longevity. They are used primarily to soften polyvinyl chloride (PVC). Note that while phthalates are usually plasticizers, not all plasticizers are phthalates. The two terms are specific and unique and cannot be used interchangeably.

<span class="mw-page-title-main">Polycarbonate</span> Family of polymers

Polycarbonates (PC) are a group of thermoplastic polymers containing carbonate groups in their chemical structures. Polycarbonates used in engineering are strong, tough materials, and some grades are optically transparent. They are easily worked, molded, and thermoformed. Because of these properties, polycarbonates find many applications. Polycarbonates do not have a unique resin identification code (RIC) and are identified as "Other", 7 on the RIC list. Products made from polycarbonate can contain the precursor monomer bisphenol A (BPA).

<span class="mw-page-title-main">Plasticizer</span> Substance added to a material to make it softer and more flexible

A plasticizer is a substance that is added to a material to make it softer and more flexible, to increase its plasticity, to decrease its viscosity, and/or to decrease friction during its handling in manufacture.

<span class="mw-page-title-main">Endocrine disruptor</span> Chemicals that can interfere with endocrine or hormonal systems

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<span class="mw-page-title-main">Bisphenol A</span> Chemical compound used in plastics manufacturing

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<span class="mw-page-title-main">Water bottle</span> Container for liquids

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<span class="mw-page-title-main">Nalge Nunc International</span> American plastics manufacturer

Nalge Nunc International is a distributor and manufacturer of plastic laboratory containers that has diversified into the field of containers for outdoor sports and packaging materials.

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<span class="mw-page-title-main">Bisphenol S</span> Chemical compound

Bisphenol S (BPS) is an organic compound with the formula (HOC6H4)2SO2. It has two phenol functional groups on either side of a sulfonyl group. It is commonly used in curing fast-drying epoxy resin adhesives. It is classified as a bisphenol, and a close molecular analog of bisphenol A (BPA). BPS differentiates from BPA by possessing a sulfone group (SO2) as the central linker of the molecule instead of a dimethylmethylene group (C 2), which is the case of bisphenol A.

<span class="mw-page-title-main">Plastic</span> Material of a wide range of synthetic or semi-synthetic organic solids

Plastics are a wide range of synthetic or semi-synthetic materials that use polymers as a main ingredient. Their plasticity makes it possible for plastics to be moulded, extruded or pressed into solid objects of various shapes. This adaptability, plus a wide range of other properties, such as being lightweight, durable, flexible, and inexpensive to produce, has led to its widespread use. Plastics typically are made through human industrial systems. Most modern plastics are derived from fossil fuel-based chemicals like natural gas or petroleum; however, recent industrial methods use variants made from renewable materials, such as corn or cotton derivatives.

<span class="mw-page-title-main">Bisphenol AF</span> Chemical compound

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Xenohormones or environmental hormones are compounds produced outside of the human body which exhibit endocrine hormone-like properties. They may be either of natural origin, such as phytoestrogens, which are derived from plants, or of synthetic origin. These compounds are able to activate the same endocrine receptors as their natural counterparts and are thus frequently implicated in endocrine disruption. The most commonly occurring xenohormones are xenoestrogens, which mimic the effects of estrogen. Other xenohormones include xenoandrogens and xenoprogesterones. Xenohormones are used for a variety of purposes including contraceptive & hormonal therapies, and agriculture. However, exposure to certain xenohormones early in childhood development can lead to a host of developmental issues including infertility, thyroid complications, and early onset of puberty. Exposure to others later in life has been linked to increased risks of testicular, prostate, ovarian, and uterine cancers.

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<span class="mw-page-title-main">Bisphenol F</span> Chemical compound

Bisphenol F is an organic compound with the chemical formula (HOC
6
H
4
)
2
CH
2
. It is structurally related to bisphenol A (BPA), a popular precursor for forming plastics, as both belong to the category of molecules known as bisphenols, which feature two phenol groups connected via a linking group. In BPF, the two aromatic rings are linked by a methylene connecting group. In response to concern about the health effects of BPA, BPF is increasingly used as a substitute for BPA.

<span class="mw-page-title-main">Health effects of Bisphenol A</span> Controversy centering on concerns about the biomedical significance of bisphenol A (BPA)

Bisphenol A controversy centers on concerns and debates about the biomedical significance of bisphenol A (BPA), which is a precursor to polymers that are used in some consumer products, including some food containers. The concerns began with the hypothesis that BPA is an endocrine disruptor, i.e. it mimics endocrine hormones and thus has the unintended and possibly far-reaching effects on people in physical contact with the chemical.

References

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  10. Potential hazards of polycarbonates in food contact applications
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