Forum Replies Created

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  • chemicalmatt

    Member
    June 27, 2014 at 5:49 pm in reply to: Suggestion for Cooling and tightening chemicals ??

    David, how about using good old witch hazel as the astringent; and why is menthol out of bounds? Frescolat is menthyl lactate if memory serves, and it will be effective at 2.0% or more (compared to 0.5% menthol).  That will get very expensive though.  How about Coolact P from Takasago also? Expensive, but cools skin OK.

  • chemicalmatt

    Member
    June 27, 2014 at 5:43 pm in reply to: SPF lip product

    SPF 15 would be the usual target, but if you are not claiming “sunburn protection” , then you need not bother claiming one at all. A little clever semantics goes a long way.

  • chemicalmatt

    Member
    June 10, 2014 at 12:23 pm in reply to: formulation with aluminium coated nano Titanium dioxide

    Rosa, there is not enough information to make a judgement here.  You did not mention the surfactant system, nor any colloid or gum you may be using to emulsify and stabilize this product, which I assume is an o/w emulsion. Also, is the Al-coated TiO2 among the “additives” you mention? If the ingredients listed above are the additives, added last, and the separation occurs before these are added, then it lends evidence of a sytemic problem, not necessarily a compatibility issue.

  • chemicalmatt

    Member
    May 14, 2014 at 10:03 am in reply to: Acronyms

    Danny, I can’t think of any one-site source explaining the acronyms you see. I assume you are referring to ingredient INCI names and such.  You’ll need to invest time in studying the chemistry of these materials.  Go to the manufacturers’ websites for a start. For beginners, know that PEG is polyethylene glycol, which is actually an epoxide polymer adducted to a carbon chain to enhance hydrophilicity, changing the HLB (hydrophile-lipophile balance) of that material.  PPG is polypropylene glycol, another epoxide adduct that also changes the HLB.  You are on your own from here on.

  • chemicalmatt

    Member
    May 14, 2014 at 9:54 am in reply to: one more study, aaaarrrggghhh!!!!!!

    Hello Millia. At least this article does not identify the alleged endocrine disrupters by name, thus sparing our industry the slander (pretty sure the authors are referring to parabens, though.) Endocrine disrupters affecting sperm motility: big deal.  Like Ruben notes, doesn’t seem to be a problem, especially in India. BTW, the most vivid endocrine disrupter of all? Sugar.  Let’s see what happens trying to ban that!

  • chemicalmatt

    Member
    May 9, 2014 at 9:51 am in reply to: Zinc chloride

    Buy the reagent grade.  You will find it has an identical assay level, just not certified as meeting all those lengthy USP standards. Your outcome will be the same.

  • gfeldman, the condition you describe is “soaping” as surmised.  It is not necessarily derived from the use of cheap ingredients, just the many anionic emulsifiers that are based on saponification (e.g. TEA-Stearic acid) and their low MW esters (e.g. glyceryl stearate). Formulas containing foaming surfactants will contribute to this as well (e.g. glucosides). You do not have to change your entire oil phase either; just add cetyl alcohol and the whitening will diminish significantly.  Be advised the viscosity will increase significantly as well.  I know I have adressed this issue here in the past, so I now have the CSNY song “Deja Vu” in my head …”we have all been here before…”

  • chemicalmatt

    Member
    April 23, 2014 at 4:22 pm in reply to: Lecithin + silicon

    Thank you Bob.  The thanks of a grateful nation is all we veterans ask, right?

    BTW, ever try to actually make liposomes using phospholipids (lecithin) and an agent to be “vesicled”?  They make it sound so easy.  It is not.  Next time somebody asks me for some, I’ll call Salvona or somewhere and make a purchase.

  • chemicalmatt

    Member
    April 22, 2014 at 9:53 am in reply to: Lecithin + silicon

    If using a high level of silicone derivatives in your formula, I recommend water-in-silicone emulsions, because they are elegant and often much less expensive, depending on the water level used, which can be significant.  Check out Dow-Corning 5225C emulsifier or DC5200 if you are also incorporating polar (botanical, vegetable) oils and esters too.  Evonik and SilTech also have equally good ( and less expensive) W/Si emulsifiers.  Check their literature for processing tips.  If you are merely emulsifying a little silicone and a little oil (< 10% total), then I recommend cationic emulsifiers.  Behenyltrimonium chloride or acid-neutralized tetiary alkyl amines (e.g. stearamidopropyl dimethylamine) work best for larger MW dimethicone (~10,000 CST +) and the various polysiloxane gums. As for lecithin, put it on your corn flakes at breakfast time for a heart-healthy phoshpolipid punch; stray away from using it in cosmetic formulations unless you are making liposomes.

  • You will not be able to incorporate any more urea than 40% (if that much), since you’ll exceed it’s water solubility saturation point.  Urea only softens skin - and callouses. It does not actually “treat” callouses or remove them like a keratolytic agent would.  That is likely the reason FDA hedged. I would classify urea creams as homeopathic remedies. They have been around for over 70 years.

  • chemicalmatt

    Member
    April 21, 2014 at 5:36 pm in reply to: Lecithin + silicon

    Assuming you mean dimethicone, kfox, the answer is: yes, you may use it, but no, it will not work. Try Plan B.

  • chemicalmatt

    Member
    April 10, 2014 at 5:48 pm in reply to: Chemical Resellers?

    Thanks, David.  I’ll contact Rowayton. I’ve got a few drums of a hair fixative polymer I want to move.

  • chemicalmatt

    Member
    April 8, 2014 at 6:08 pm in reply to: Theobroma cacao shell powder

    VInta, check out food ingredient suppliers in your area for both cocoa shell powder and salt. Their prices tend to be lower than the distributors peddling to the personal care industry. Salt can be had from any industrial chemical supplier also.

  • chemicalmatt

    Member
    March 31, 2014 at 10:09 am in reply to: how to change o/w to w/o?

    Before you get too far using that article linked from makingcosmetics.com, cherri, be advised there are glaring misrepresentations in that article about inverse-phase emulsions. Do not add polymeric thickeners to the internal (water) phase - ever - unless you really want to drive yourself crazy. I don’t know where they came up with that one, but it is categorically wrong. (Who writes this stuff?) Also, magnesium sulfate works better than NaCl in stabilizing W/O emulsions about 90% of the time, so start with epsom salt always.  That article also fails to mention the best W/O emulsifiers in existence, the silicone-based ones.  See Evonik, Siltech and Dow-Corning product guidelines for these. In case you haven’t deduced this yet: you have to begin from scratch here; you cannot simply “change” from O/W to W/O.

  • chemicalmatt

    Member
    March 28, 2014 at 10:09 am in reply to: French Clay Masks

    Maya, bentonite, laponite or good old Veegum (magnesium aluminum silicate) would solve your stability issue, even with the oils incorporated.  Clays tend to deactivate formaldehyde donor preservatives, (and others I suspect), especially when added after incorporation.  Always add your preservative first to the water, before adding the clays and colloids. Perhaps someone else in the Forum knows the best preservative to use with clays. I have to believe simpler molecules like benzyl alcohol, sodium benzoate, sodium dehydroacetate would do well; PCMX would be a slam-dunk.

  • chemicalmatt

    Member
    March 26, 2014 at 2:09 pm in reply to: face cream

    Do not ever be embarrassed asking for advice on this forum,chicagogirl.That’s why Perry ( a Chicago boy like me) founded it.  We studied chemistry and physics so you didn’t have to. FYI, the solvent concentration (water in this case) does affect penetration too.  Less water, less penetration.  Also, you may have a case here of less is more.  I don’t think you need more than 1.0% dl-panthenol in a o/w lotion to be effective in softening the skin. Add a little urea and all the better. Cheers.

  • Kim, assuming there is no SDA (ethanol) in this toner, and the pH is in the 5.6 - 6.5 range, why not switch to Geogard 221 (benzyl alcohol & dehydroacetic acid)? Safety profile and regulatory status is the same.

  • It won’t.

  • chemicalmatt

    Member
    March 25, 2014 at 5:29 pm in reply to: Beeswax (without borax)

    I cannot think a beeswax-borax w/o emulsion would be stable without the borax.  Those who claim stability likley had a very high level of lipid components and likely at least one other low HLB surfacatant without knowing it.  I have a lot of experience with these formulas and its intriguing to think of them as a “nouveaux” natrural emulsifier, which of course they are. There is no other w/o emulsifier as natural as this, by the way. The glucosides are chemically modified. Beeswax is also useful as a stabilizer in w/o emulsions using other emulsifiers, which can also use microcrystalline wax for the same purpose.  Beeswax is not cheap these days, like it was only ten years ago, but you may be onto something here in exploring its use.  White beeswax with an Acid Value of 17 - 24 works best as I recall.

  • chemicalmatt

    Member
    March 25, 2014 at 5:11 pm in reply to: Few questions for the chemists

    SPF testing is expensive, but here goes: in the Eastern U.S. try Essex Testing; in the Midwest try Advanced Testing Laboratory; in the Western U.S. try Bioscreen Testing Services.

     

    One (1) cfu is absolutely nothing to worry about.  Usually that would be annotated as <10 cfu/ml, which is well within acceptable control limits.

     

    Perry & Making are correct in their assessment. Given the high profile given the naturals, this formulator conveniently left out the unnatural ingredients.  This is a common scam within the “natural cosmetics” industry.  And, they likely did process this at 35 - 40C by using an associative thickener to hold it all together, e.g. Seppigel 305 or what not. Listing all that neat almost-edible stuff would be undermined by also listing “Acrylamide” too.  There oughta’ be a law! Oh wait, there already IS one. 

  • chemicalmatt

    Member
    March 21, 2014 at 3:36 pm in reply to: Penetration Enhancers- Which ones to use?

    Yup…..that’s the isosorbide thingy allright.  Arlasolve DMI (dimethyl isosorbide)?  Not an ester either, but a modified heterocycle. Another strangely expensive chemical too if I recall. Even more so now that Croda markets it, I suspect.

  • chemicalmatt

    Member
    March 21, 2014 at 10:43 am in reply to: Surfactant in face wash

    You need to know your nomenclature for fatty acid homologs: deceyl = C10, dodecyl = C12, Lauryl = C14, Palmitic = C16, Stearyl = C18, Behenyl = C22, all saturated carbon chains. Unsaturated ones (olefins) have different names. Perry ought to add a link someplace to study these. You cannot go wrong with coco glucosides, though building viscosity is a small hurdle to overcome, you are well advised to make it the base surfactant for your wash and begin from there. I do not have much experience with SMC Taurate, though I do know it was used early on in the “sulfate-free” game.  The glucosides and sarcosinates are less expensive and foam better than the taurates, if memory serves. Those glutamates are superb - but wierdly expensive in my opinion. Glycerin is vastly over-rated in body washes, for the reasons mentioned earlier.

  • chemicalmatt

    Member
    March 21, 2014 at 10:21 am in reply to: Penetration Enhancers- Which ones to use?

    Though philosophically I’m with Bob Zonis on the subject, here are some cues I’ve experienced.  Liposomes (phospholipid vesicles you can make with lecithin) are designed to penetrate the stratum corneum while carrying a “payload” of vitamin E or whatever lipid can fit within.  Emu oil (kalaya oil in some parts) has pronounced penetrating properties and has even been known to cross the blood-brain barrier.  Ethoxydiglycol has the property of enhancing penetration of the hair cuticle inot the cortex with small molecule components (e.g. NaOH, LiOH).  Unfortunately, it also halps penetrate the scalp with those same alkali - ouch!  Then there is that isosorbide ester ICI (now Croda) has that allows triglyceride oils to penetrate into the subcutaneous layer. I forgot its name.

    (Hey Perry, now that the glaciers have receded from North Avenue here in Chicago, start joggling again, clear your brain with fresh air, and come up with an article about this topic.)

  • chemicalmatt

    Member
    March 20, 2014 at 4:30 pm in reply to: Waxes for thick cream

    Gustavo, ozokerite is part of the petrochemical (mostly) linear alkyl homolog family of petrolatum/microcrystalline wax/ozokerite/paraffin.  It is very useful in thickening and stabilizing mineral oil, petrolatum based emulsions, even the water-in-oil ones, and can harden those cyclomethicone-stearyl alcohol antiperspirant sticks like nothing else ( I’m talking 0.10%!). The others are natural waxes, more polar, complex and vary softeness and pliability in lipsticks, lipbalms, color make-up pencils.  I never tried burning some to see what happens.  Could be a renewable fuel!  Perhaps another forum member more versed in color cosmetics can help here.

  • chemicalmatt

    Member
    March 20, 2014 at 4:20 pm in reply to: Lactic acid emulsion not stable

    Makes sense, Mike. I thought Stepan made this creature, Even better might be the Pationic lactylate surfactants from R.I,T.A., which work well as primary emulsifiers, though the R.I.T.A. literature strangely doesn’t mention that.  Pationic SSL is what I remember using (stearoyl lactylate). I can also tell you I remember an article years ago noting that lactic acid and its salts actually stabilize urea from hydrolytic decomposition, so you are probably in good shape here. The old 10% Urea skin-care creams used that trick. 

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