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Bluebird
Forum Replies Created
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You could try adding NoOH to the solution before adding chitosan, maybe.
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This reply was modified 3 days, 21 hours ago by
Bluebird.
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This reply was modified 3 days, 21 hours ago by
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Bluebird
ScientistSeptember 21, 2024 at 6:46 am in reply to: Mold preservation with sodium benzoateIt’s a very watery toner/serum type formulation. No oil or sugar.
I can’t use a chelator because I may have to add a zinc salt in one of the formulations so that won’t quite work with a chelator, I’m thinking.
Package won’t be as invasive as a finger-in-cream type; it will be most likely a spoid-type dropper dispenser, which does have a chance of contamination form users.
As for glycol I can increase it a bit in some formulations. Would, say 10% propanediol significantly help preservation instead of 5%?
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Caffeine 5% in water seems way too high to be stably soluble.
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Bluebird
ScientistJanuary 14, 2024 at 6:55 am in reply to: Solubility of caprylhydroxamic acid in phenoxyethanol or glycerinThis mix may clash with this (rather annoying) Inolex patent. Because of the use of CHA and methylpropanediol in percentages covered in Claim 1.
“1. A preservative composition blend comprising about 4.5% to about 15% caprylohydroxamic acid or a salt thereof, wherein caprylohydroxamic acid is the only hydroxamic acid in the composition blend, and about 7% to about 95.5% of a diol selected from the group consisting of a propanediol, methylpropanediol, a butylene glycol, 1,2-pentanediol, 1,2-hexanediol, caprylyl glycol, 1,2-decanediol, caprylyl glyceryl ether, ethylhexylglycerin, glyceryl monolaurate, glyceryl monocaprate, glyceryl monocaprylate, and combinations thereof.”
https://patents.google.com/patent/US10897899B2/en
patents.google.com
US10897899B2 - Preservatives for cosmetic, toiletry and pharmaceutical compositions - Google Patents
A composition for and methods of preserving a topical cosmetic, toiletry or pharmaceutical formulation against microbiological contamination or growth are described in which the compositions used herein include at least one hydroxamic acid, salt or complex thereof, and the methods … Continue reading
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Bluebird
ScientistJanuary 14, 2024 at 7:26 am in reply to: Solubility of caprylhydroxamic acid in phenoxyethanol or glycerinThere’s also this patent, which is even more broad than the one I shared before.
US/8993641/B2
It looks to me that any use of CHA with diol in the US without using Inolex’ product is blocked but I am hoping I’m wrong.
Did you find a clever way to go around this?
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Bluebird
ScientistJanuary 14, 2024 at 4:57 am in reply to: I recently got molds on a formula that worked beforePotassium sorbate is not good for eczema, trust me… or better still, let your sister test and tell us what she says, haha.
Also if you want to use pot sor you’ll need lower ph like 4-4.5 for efficacy.
Could be jar contamination or incomplete mixing.
Can consider refrigerating and only using for one week or two.
That’s what I do sometimes for my super sensitive skin.
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Could be that the new preservative mix is more sensitive to the product pH, for there is benzyl alcohol, which may need low pH for efficacy. Just a guess.
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Thanks. But I wonder. When I did test it on microbial testing, they actually killed Gram positive and negative bacteria (cap+1,2 hex) in broth full of bacterial food. And a product I used for over a year in the bathroom, preserved with only low percentage of the above, did not have any bacterial growth (0 CFU) when I tested. But I’m aware that they are mentioned as preservative boosters commonly; I wonder why.
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Bluebird
ScientistFebruary 22, 2025 at 9:17 pm in reply to: Hair softening ingredients in shampoo to use along with a nonionic surfactant.These should be compatible with coco-glucoside as the surfactant (nonionic) and lowish pH (~5), right? 🙂
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I’m thinking of pH 4.7-5.5 and anti-bacterial and anti-yeast preservatives are caprylyl glycol and 1,2 hexanediol. I suppose I can add sodium benzoate.
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Bluebird
ScientistFebruary 22, 2025 at 8:31 pm in reply to: Hair softening ingredients in shampoo to use along with a nonionic surfactant.Thank you!
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thank you!
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Bluebird
ScientistFebruary 18, 2025 at 7:31 pm in reply to: Mixing different glucosides- does that make much difference for face cleanser?Oh, got you. Thank you!
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How about Sodium benzoate + 1,2 hexanediol then, for low pH (ex, 4-5)?
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Rancid due to oxidation, yes. I did try vitamin E but that did not help. Though another antioxidant may work, I doubt it because the smell lasts a long time once applied (ex, a week or more) even after washing and it seems the original oil pulls out metal from hair/scalp and the metals kind of sit there despite washing, and then continue to react not with the original oil that was used, but with human sebum. People have higher metal contents due to various reasons. Some lack certain vitamins (esp. vitamin B) that help the process of removing heavy metals from the body. Others may be continuously using some products or eating food that have higher metal contents. I personally did one of these hair/scalp metal test and found aluminum was higher than normal/average. And I of course reacted rather badly with this oil as well.
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Not to protect the product, but rather there is a specific oil I want to use that are good for a certain skin condition, but for an individual who has high metal contents in hair or scalp, but this oil is suspected to react fast (within hours) with metals and create funny smell; hence I wondered whether there was any oil soluble chelators to capture metals on scalp once this oil was applied.
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Bluebird
ScientistSeptember 21, 2024 at 4:42 am in reply to: Mold preservation with sodium benzoateHi, there is no chelating agent.
Currently I’m testing with 0.5% of (caprylyl glycol and 1 2 hexanediol mix); the manufacturer recommends 0.5% but does not disclose the proportion of cap glycol and hexandiol, unfortunately. I am thinking of perhaps adding a bit more of hexanediol on top of this to be safer.
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Bluebird
ScientistAugust 18, 2024 at 2:16 am in reply to: Why is there a ban on vitamin D in EU? Anyone knows the reason they gave?I have of course tried it already and I have not found the answer to my question still
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Bluebird
ScientistAugust 16, 2024 at 2:01 pm in reply to: Why is there a ban on vitamin D in EU? Anyone knows the reason they gave?Though this one is not from EU, I guess that has to do with dosage concern.
Here, apparently Canada regulates it, too, in cosmetics,
List of Ingredients that are Prohibited for Use in Cosmetic Products
“Average daily absorption must be equal to or less than 25 µg per day.”
Still haven’t found the exact details of the restriction deal in EU.
canada.ca
Cosmetic Ingredient Hotlist - Canada.ca
The Hotlist is used to keep the cosmetic industry aware of substances that are restricted or prohibited in cosmetics
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Bluebird
ScientistAugust 16, 2024 at 1:49 pm in reply to: Why is there a ban on vitamin D in EU? Anyone knows the reason they gave?I’m talking about vitamin D ban in cosmetics, not as oral supplement!
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Bluebird
ScientistAugust 16, 2024 at 1:43 pm in reply to: Why is there a ban on vitamin D in EU? Anyone knows the reason they gave?Can you share where you found that EU bans only particular brands’ vitamin D?
From my search, they ban vitamin D2 and D3, which are final forms of vitamin D, not vitamin D from any brand in particular.
They do allow pro-vitamins, which are not truly vitamin D in their final forms.
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This reply was modified 6 months, 1 week ago by
Bluebird.
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This reply was modified 6 months, 1 week ago by
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Bluebird
ScientistJune 15, 2024 at 7:25 pm in reply to: Propylene glycol vs propanediol allergy/irritationSo sensitization= allergic contact dermatitis, then.
Earlier you mentioned neither PD nor PG is a skin sensitizer.
And yet there are people whose allergy patch panel test shows as positive to PG for a fact
(PG is tested in several concentrations in a patch test).
So am I interpreting it right that when you said PG was not found as a skin sensitizer,
you meant it’s not an ingredient that commonly causes allergic contact dermatitis?
(That allergy is rare?)
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Bluebird
ScientistJune 14, 2024 at 7:29 pm in reply to: Propylene glycol vs propanediol allergy/irritationThanks, these papers are nice to have.
I’m mostly wondering about allergy, not sensitization/irritation, though I did mention all of those words with regards to anecdotes and that could have clouded my meaning.
I’m wondering whether someone who tested positive in a patch allergy test to PG is likely to be also allergic to PD. This is not really in the realm of chemistry as it’s about allergens and immune reactions. I am asking in case folks long in the cosmetics industry have heard about it either way.
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Is this how it works, though?
When you lower pH of the salt of an organic acid, wouldn’t you still expect higher solubility than its organic acid counterpart in low pH, because there is the balancing counter ion?
Ex, sodium benzoate solubility in water is high even in low pH;
but apparently the benzoic acid solubility in water is low, less than 0.2%.
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you mean visually inspect of every single bottle before using it in semi mass production?
Or you mean visually inspect random few to get an idea?
Also why do you expect/are concerned most about Gram neg bacteria in tap water as opposed to mold, yeast etc? Are they just more often found in tap water than others