Using Powder that is probably 40+ years old

The rotten egg smell of powder going bad is unmistakable, and fairly pungent. And, the chemical degradation will add the reddish discoloration.
No bad smell, no discoloration, no clumping of powder means you're likely safe to use it as directed.

Reddish/brown fume is nitric acid and ANY powder displaying that symptom needs IMMEDIATE DISPOSAL , as in lawn garden fertilizer or spread outside in a safe area and light it ,so it can burn off . Binding of powder and coatings belongs to ethyl acetate . If any of you are or were wood workers , you might know that product as Resorcinol aka water proof adhesive . Yep the old Purple resin and powdered catalyst super wood glue .

See Chemistry is Interesting ;:)

Propellants consisting of nitrocellulose and/or other nitric esters are
inherently chemically unstable and undergo decomposition even under standard
storage conditions. Their decomposition can be inhibited or nearly stopped
when approximate stabilizers are used. However, conventional stabilizers
form nitrosamines that have toxic and carcinogenic effects. Therefore, these
conventional stabilizers should be replaced as soon as possible.
In general, chemical stabilizers are substances capable of the chemical
binding of decomposition products of, above all, nitrocellulose and other
nitroesters used for the production of smokeless powders

Nitrocellulose and nitroglycerin are energetic bases for smokeless powders, because they can be used as propellants, and their burning produces much less residues than that of black powder . All smokeless powders can be placed into one of three different classes according to the chemical composition of their energetic ingredients. A single-base powder contains nitrocellulose, whereas a double-base powder contains nitrocellulose and nitroglycerine. Nitroguanidine can also be included as a third energetic base, forming a triple-base propellant . In some cases, nitroglycerine can be replaced by nitroglycol because it is more stable at lower temperatures than nitroglycerine

Below is Copied from My Hercules Manual ;

Stabilizers such as diphenylamine, 2-nitrophenylamine, dinitrotoluene, A-methyl-p-nitroaniline, centralites, or acardites (e.g., AW-diphenyl-urea), to increase chemical stability by combining with decomposition products.

A range of inorganic additives such as chalk, graphite, potassium sulfate, potassium nitrate, barium nitrate, to improve ignitability, facilitate handling, and minimize muzzle flash. (Graphite acts as a lubricant to cover the granules and prevent them from sticking together and it also helps to dissipate static electricity).
 
Found a box of 40 rounds of 22-250 ammo I loaded over 27 years ago hiding in my loaded ammo cabinet. According to the load data on the box they are 55gr Sierra SPBT bullets loaded with 38.0 Grs of H-414, CCI 250 primers, new Federal cases and a COAL of 2.380". This was my most accurate ground hog load many, many years ago in my factory M700 Remington heavy barrel rifle. Sighted in at 100 yds it would put 5 rounds thru a dime starting with a cold barrel on the first shot day after day with calm weather. I am anxiously awaiting the return of this rifle after the addition of a new Lilja 1-8 twist barrel from my gunsmith. I originally bought this rifle in 1974 I think.
 
Ether is used as a solvent.
If powder smells of ether (aka starter fluid) it’s likely still good.

If it smells like “old aspirin” or Vinegar, likely bad.

If has red dust, feed it to the azaleas !
 
Old powder?
I’m still using Hodgdon military H-4831 that I bought in 1973. It’s WWII or Korean conflict vintage at newest. It was better than current H-4831SC last time I compared the two about 10 years ago. I still have some in the big square galvanized 50# powder kegs and it looks and smells like new.
Anybody got any older powder they still use?
 
Reddish/brown fume is nitric acid and ANY powder displaying that symptom needs IMMEDIATE DISPOSAL , as in lawn garden fertilizer or spread outside in a safe area and light it ,so it can burn off . Binding of powder and coatings belongs to ethyl acetate . If any of you are or were wood workers , you might know that product as Resorcinol aka water proof adhesive . Yep the old Purple resin and powdered catalyst super wood glue .

See Chemistry is Interesting ;:)

Propellants consisting of nitrocellulose and/or other nitric esters are
inherently chemically unstable and undergo decomposition even under standard
storage conditions. Their decomposition can be inhibited or nearly stopped
when approximate stabilizers are used. However, conventional stabilizers
form nitrosamines that have toxic and carcinogenic effects. Therefore, these
conventional stabilizers should be replaced as soon as possible.
In general, chemical stabilizers are substances capable of the chemical
binding of decomposition products of, above all, nitrocellulose and other
nitroesters used for the production of smokeless powders

Nitrocellulose and nitroglycerin are energetic bases for smokeless powders, because they can be used as propellants, and their burning produces much less residues than that of black powder . All smokeless powders can be placed into one of three different classes according to the chemical composition of their energetic ingredients. A single-base powder contains nitrocellulose, whereas a double-base powder contains nitrocellulose and nitroglycerine. Nitroguanidine can also be included as a third energetic base, forming a triple-base propellant . In some cases, nitroglycerine can be replaced by nitroglycol because it is more stable at lower temperatures than nitroglycerine

Below is Copied from My Hercules Manual ;

Stabilizers such as diphenylamine, 2-nitrophenylamine, dinitrotoluene, A-methyl-p-nitroaniline, centralites, or acardites (e.g., AW-diphenyl-urea), to increase chemical stability by combining with decomposition products.

A range of inorganic additives such as chalk, graphite, potassium sulfate, potassium nitrate, barium nitrate, to improve ignitability, facilitate handling, and minimize muzzle flash. (Graphite acts as a lubricant to cover the granules and prevent them from sticking together and it also helps to dissipate static electricity).

Helluvan explanation here! Thanks.
Where/when/ what powders contain this carcinogenic compound?
The oldest powder I have currently s a batch of Ww-231 from 1998, and a batch of 2400 from 1999. Then everything else is from 2010 and newer.
The powders from the late 90s look, smell, load and shoot as if brand new, notice no difference..... thanks in advance for your reply.
 
Assuming it looks, smells, and burns right, I would load that up and then I'd load up another batch with a fresh can of the same powder with the same brass, bullets, primers, load data, etc and then I'd compare the velocities of the two powders with a good chronograph and then I'd submit that velocity data to THR reloading forum for consideration. I think it would be very interesting and informative.
 
I started out loading 52.5 gr 4064 with a Sierra 150 gr bullet in 1975.

Still shooting the same load. No need to change.


Smell the powder. If it doesn't read of vinegar, choose it!

I have several cans of those old DuPont powders from the '80s, all get used.

The ONLY questionable powder I ever had, was from the '50s. Have shot several that were much older.
 
Like the others, I have used powder that old or older. If it passes those simple test I would load it and shoot it.

A worthwhile thing to remember. If you are buying powder in quantities where you are likely to keep it for long periods of time store it in a controlled environment and out of the direct sunlight. Actually, powder should be stores this way no matter how long it will take you to use it.

Another thing that I do is I write the purchase date on the container. This helps me to use the oldest stock first.
 
Old powder?
I’m still using Hodgdon military H-4831 that I bought in 1973. It’s WWII or Korean conflict vintage at newest. It was better than current H-4831SC last time I compared the two about 10 years ago. I still have some in the big square galvanized 50# powder kegs and it looks and smells like new.
Anybody got any older powder they still use?

Yes I purchased a couple of 5 lb. cardboard tubes of H870 ,via mail from Hodgdon's in 1963 and again in 1965 and still have about 2 lb. maybe .
I've yet to find it's equal in MY 7mm RM . A fair # of animals would if they could attest to that also . I purchased more over the years and did put the old powder into empty sealed canisters . I also Filled them right up to the top ,so as to minimize air aka oxygen and put seals on the cans lids. I also marked said canisters with India Ink and clear tape over that ,it's fully legible after all this time . My powder was ALL stored at 56 Deg. constant temp with No visible light . Until we moved ,then I had to make arrangements but all seems JUST FINE so far . H870 powder.jpg
 
Helluvan explanation here! Thanks.
Where/when/ what powders contain this carcinogenic compound?
The oldest powder I have currently s a batch of Ww-231 from 1998, and a batch of 2400 from 1999. Then everything else is from 2010 and newer.
The powders from the late 90s look, smell, load and shoot as if brand new, notice no difference..... thanks in advance for your reply.

Powders still contain carcinogenic compounds , Primers have and are being made with out Lead styphnate ,which is an acid by the way ; styphnic acid . Nitro is a fume compound of Sulfuric and Nitric acids ,when ignited produces undesirable toxic gas .

Before anyone goes bananas , Firearms have chambers and the operator hopefully isn't sucking the fumes out the barrel . If one reads the Hazardous cautions of Hodgdon's link ,it explains it better than I can . Diphenylamine CAN Attack liver & Kidneys aka carcinogenic fyi Lead is also .

Below Copied in reference to a well know smokeless powder stabilizer diphenylamine
Toxicity
In animal experiments diphenylamine was rapidly and completely absorbed after ingestion by mouth. It underwent metabolism to sulfonyl and glucuronyl conjugates and was rapidly excreted mainly via urine. Acute oral and dermal toxicity were low. Diphenylamine can cause severe irritation to the eyes. It was not a skin irritant, and it has not been technically feasible to test acute toxicity study by inhalation. Diphenylamine targets the red blood cell system and can cause abnormal erythropoiesis in the spleen, and thus congestion of the spleen, and haemosiderosis. Changes in liver and kidneys were found upon longer exposure.[6] At clear toxic doses of parent animals reproductive effects were limited to reduced implantation sites in F1 females associated with reduced rat litter size, implicating a possible mutagenic or teratogenic effect. No effect on development could be attributed.[6] The U.S. CDC's NIOSH lists the following symptoms of poisoning: irritation eyes, skin, mucous membrane; eczema; tachycardia, hypertension; cough, sneezing; methemoglobinemia; increased blood pressure and heart rate; proteinuria, hematuria (blood in the urine), bladder injury; in animals: teratogenic effects.[23]

The short-term NOAEL of 9.6 – 10 mg/kg bw/day was derived from 90-day rat, 90-day dog and 1-year dog studies and the long-term NOAEL was 7.5 mg/kg bw/day. The Acceptable Daily Intake of diphenylamine was 0.075 mg/kg bw/day based on the 2-year rat study, applying a safety factor of 100; the Acceptable Operator Exposure Level was 0.1 mg/kg bw/day.[6]

In a study of diphenylamine metabolism in harvested and dipped apples at different time intervals it was observed that radiolabelled residues of diphenylamine penetrate from the surface into the pulp, which after 40 weeks contained 32% of the residue. Diphenylamine was always the major residue, but 3 metabolites were found in good amounts in the apple samples, whose identification experts considered insufficient.(Kim-Kang, H. 1993. Metabolism of 14C-diphenylamine in stored apples—nature of the residue in plants. Report RPT00124. Study XBL 91071. XenoBiotic Laboratories, Inc., USA, unpublished) cited in [6][24] There is a data gap on presence or formation of nitrosamines in apple metabolism or during processing.[6] The carcinogen 4-Aminobiphenyl can accompany diphenylamine as an impurity.[23]

Diphenylamine has low acute and short-term toxicity to birds, but is very toxic to aquatic organisms. Risk to biological methods of sewage treatment was assessed as low.[6]

The impurity in commercial diphenylamine which induces polycystic kidney disease in rats was identified in 1981. Laboratory studies with highly purified diphenylamine indicated that the impurity can be formed by heating diphenylamine

https://www.ilrc.ucf.edu/powders/documents/powder 00000371/Hodgdon_H110.pdf


Here's data on primers Naval Warfare Center :

The Naval Surface Warefare Center Indian Head Division (NSWC-IH) has demonstrate KDNP as a drop-in replacement for lead styphnate in the primers used in ammunition and cartridge actuated devices. The Al/Bi2O3 MIC composition provides comparable or superior performance to current military lead styphnate formulations such as FA-956 (No. 41 primer for all 5.56mm, 7.62mm and .50 cal ammunition) and 5086 (PVU-1/A primer for CAD/PAD applications).
 
^^^^^I have the same^^^^^ Bullseye and Blue Dot containers. Just yesterday, I finished up loading all of the Blue Dot in some 124 gr. 9MM ammo and cracked open the sealed Bullseye container to use soon. Both containers are from the late 1980's.

I tested the Blue Dot a week ago with some test loads @ 7.0,7.5 & 8.0 grs. All shot fine. I loaded the 1000 rounds with the 7.5 load.

Recently, a friend gave me a full 1/2 # container of Alcan 7 from the 1960's. The can and powder looks like it was made yesterday.

I have old loading data and will use it up in in some 38/357 and 41 Mag. loads.

I've shot up a lot of old powder. Old powder works fine as long as it's been checked for deterioration. I've had some old powder that went bad and had to toss it. It's pretty easy to recognize.
 
The whys and wherefores of nitrocellulose (or Cellulose Nitrate) stability is a very involved topic. This is an interesting document, of which I have only copied a few paragraphs. Cellulose nitrate stability is a real concern with museums. You can read about the fears of old film stock autocombusting, and more interesting, the forgotten history of nitrocellulose film stock autocombusting and burning down movie theaters, with of course, loss of life. Those forms of cellulose nitrate are less highly nitrated than gunpowder, but they still will catch fire.


The Use of Cellulose Nitrate in Art Conservation

Dr. Charles Selwitz Getty Museum

https://www.getty.edu/conservation/publications_resources/pdf_publications/pdf/nitrate.pdf

Cellulose nitrate is the polynitrate ester of the natural polysaccharide, cellulose, and for a polymer averaging 2.3 nitrate groups per glucose unit has the structure shown in Figure 1. The molecular weight for most commercial products ranges between 20,000 and 250,000. This semisynthetic polymer was first produced more than 150 years ago and is the most important and only commercially available inorganic ester of cellulose. Due to its unique physical properties and low cost it has been an important factor in many advances in the industrial arts and sciences over the years. Cellulose nitrate was initially used in the manufacture of military explosives where it came to be known as "gun cotton," the first major development in explosives since the introduction of black powder. When it was discovered that cellulose nitrate could be stabilized with camphor (in the ratio of 4:1), the resultant product, celluloid, inaugurated the advent of engineering plastics

In the years following World War I, cellulose nitrate lacquers and coatings were developed. While these have since been superseded by better materials, the largest industrial use today of cellulose nitrate (now also referred to as nitrocellulose) continues to be in its capacity as a lacquer, although substantial quantities are still used in explosives and propellants, printing inks, and plastics. Currently, the total commercial production of cellulose nitrate in the United States approaches 100 million pounds a year

in terms of stability, however, cellulose nitrate is a very suspect material. It does not have the resistance to degradation possessed by most other polymers used in conservation. Only when stability is defined as "the maintenance of solubility and reversibility" can cellulose nitrate, which degrades, but generally does not crosslink, be said to have stability


Chapter 3 Causes of Instability

Most of the literature on cellulose nitrate instability describes three primary modes of decomposition: hydrolytic, thermal, and photochemical. These modes are examined in this paper with concern for rates and mechanisms most likely to prevail under ambient conditions. Recent research can be interpreted to show that these three modes can be redefined into more fundamental mechanisms for primary decomposition, a finding that may provide additional insight into the properties of the polymer as well as the optimum conditions for its use. Primary decomposition processes slowly lead to breakdown products. If these are not swept away they can lead, catalytically, to a faster and more extensive degradation than that caused by the primary processes that engender them. Conclusions on the chemistry of decomposition caused by these breakdown products, i.e., secondary processes, are integrated with our analyses of the primary modes in the next section-a discussion on the overall stability of cellulose nitrate at ambient conditions.

Hydrolytic Decomposition via Acid Catalyzed Ester Cleavage

The earliest manufacturing processes of cellulose nitrate in the 19th century were concerned almost totally with the production of explosives. After a number of disastrous detonations took place, the search for their causes revealed in 1865 that the retention of small amounts of sulfuric acid from the nitrating mixture was responsible for the instability (Worden 1921:1604 et seq.), and, further, that this instability was roughly proportional to the amount of sulfuric acid left in the polymer (Wiggam 1931:536). It was also recognized that sulfate esters of partially nitrated cellulose were also formed (Hake 1909:457). In no case did the nitration of cellulose with mixed acid ever proceed to a completely nitrated product, i.e., to a D.S. of 3.0 and nitrogen content of 14.1%. The best that could be achieved was a product with 13.8% nitrogen in which only 29 out of 30 hydroxyl groups bore nitrate functionality because the 30th was converted to a sulfate ester. In cases where exhaustive nitration was done without using sulfuric acid, e.g., with nitrogen oxides (Bouchonnet et al. 1938:308) or with nitric acid and phosphorus pentoxide (Lenz et al. 1931:4) or acetic anhydride, a completely nitrated product 15 Instability with 14.1% nitrogen was obtained. These products were invariably of better stability than high nitrate product made with mixed acid (Barsha 1954:724-30).

The lifetime of your cartridges is not just a simple of where you store your ammunition, but storage is very important, particularly temperature. This is from a Nato specification, I removed the number due to the number of conspiracists who discounted the information because they believe Nato is out to create a one World Government.

Gunpowder deteriorates exponentially with temperature.

rPNzqCj.jpg

I found this chart from a 1970 Symposium, it more or less shows what the Army was doing in terms of stockpile reliability testing

056KrAU.jpg

The thing is, the lifetime of gunpowder is an unknown, and it has to be determined by testing.

For those who have WW2 era 4831, well I have some. And I have some cartridges loaded by the man who gave me a can of the stuff. The ex Gun Club President sold me a 300 Win Mag and tossed in ammunition he had loaded with WW2 surplus 4831. I cannot say it was IMR 4831 as it could have been made in a military Arsenal. Pres says the stuff was so cheap one of the guys on the buy was using it as to light the charcoal for his barbeque!

Anyway, I started going through the ammunition and became very concerned about the boxes loaded with “H4831” or simply “4831”. I verified with Pres that was his notation for the WW2 era 4831.

yCPKlf6.jpg

gNTfHWN.jpg

sg1sAHZ.jpg

uSnkV2S.jpg

The powder does not look gummy or dusty. Is it safe?

nOarAmS.jpg

When Pres gave me the can (2013ish) I took it out and tested it with new IMR4831 in a 270 Win rifle. I did not notice any anomalies. It burnt faster than the new stuff, but, this is not blended IMR 4831. The stuff we get is blended to an average pressure curve. The military has its own pressure gauges and chronographs, so they test lots and determine how much to put in the case.

80TsJID.jpg

So again, is it safe? Heck if I know, what I do know is it is showing signs of deterioration. I sure as heck discarded the corroded 300 Win Mag cases, and the old powder. The thing is, for me, there are a number of known unknowns I have about old powder. I don’t know how to tell if the burn rate is unstable before shooting it. I did have sticky extraction with “funny” retorts with military pull down IMR 4895. That powder looked good and did not smell. It also cracked the case necks of 700 LC308 brass. I considered those signs as a portent of evil things ahead, so I stopped shooting the stuff. I also don’t know the level of deterioration it takes for smokeless propellant to detonate.

Old gunpowder does not burn predictably as the shape and chemistry of the grain has changed. It may not blow up your firearm each and every time, but there are plenty of blow up reports with old factory ammunition. Notice in all the powder recalls in magazines, a warning not to load ammunition with the deteriorated gunpowder. A huge concern with the Insensitive Munitions community is keeping deflagrating propellants from transitioning to detonating propellants! https://en.wikipedia.org/wiki/Deflagration_to_detonation_transition Energetic propellants should not be considered 100% predictable, nor something under your control. * Everything I have read indicates the Insensitive Munitions community would like a solid and definitive theory of burning, but they don't have one. They have empirical models, and there are limits to their knowledge, such as the exact conditions that it takes deteriorated powders to develop burn rate instability and detonate.

This writer had 1960’s 22 lr blow up his pistol. Why Did My Gun Blow Up? https://www.activeresponsetraining.net/why-did-my-gun-blow-up

Some people want absolute certainty before they will commit to a path to action. Life is seldom that certain. Anyone remember the Surfside Florida Condo collapse? https://en.wikipedia.org/wiki/Surfside_condominium_collapse The condo owners totally ignored and disregarded the severity of the structural issues of their building. The geezer condo owners preferred to kick the maintenance can down the road. For the old folks this was an economically rational decision. Why spend money now, when their life expectancy is less than the building? So, they took the risk of having the building fall on them while they were still up right. Ninety eight of the condo owners did lose that bet when they were crushed in the collapse, and the living all lost their condo’s. But the Gods do laugh, except for those who lost their lives, the survivors came out winners as they sued enough entities to get an award of $1.0 billion dollars!

If you can sue someone when the roof falls on top of you, maybe the termites eating the structure of your house are actually doing you a favor. Or your grandkids a favor, assuming you get flattened. Seems our society is based on the concept we are all victims of somebody. Maybe someone knows the odds of winning a case against an ammunition company when something goes bad with your old ammunition. It used to be ammunition companies warranted their ammunition for ten years. Now it looks like, one year.

https://www.cci-ammunition.com/warranty.html

Warranty FEDERAL PREMIUM – CCI – SPEER – BLAZER – AMERICAN EAGLE LIMITED WARRANTY

CCI/Blazer warrants its ammunition and primers to be free from defects in workmanship and materials for a period of one (1) year from the date of purchase. This warranty is extended only to the original consumer purchaser.
 
I'm still loading (and shooting) IMR-4198, IMR-3031 and Winchester 748 powders that date back to the 1980's.

They still all deliver velocities of between 96% and 98% of what they did in the 20th Century. I take that to mean any deterioration in the intervening decades is trivial.

But as a caution, my 1980's vintage Green Dot did suffer significant deterioration and is no longer used.
 
I'm still loading (and shooting) IMR-4198, IMR-3031 and Winchester 748 powders that date back to the 1980's.

They still all deliver velocities of between 96% and 98% of what they did in the 20th Century. I take that to mean any deterioration in the intervening decades is trivial.

But as a caution, my 1980's vintage Green Dot did suffer significant deterioration and is no longer used.

The thing is, look, and sniff your gunpowder. If it smells bitter, don't reload it.

gYgK0S0.jpg

this would be a good candidate to toss

KYSquJE.jpg


this too

Z03JC41.jpg


I would not used clumped gunpowder.

OSW5VUq.jpg

bad smells and physical evidence of deterioration are proof positive that the powder is risky to use.

However, the powder can still have a neutral smell, and look good, and yet give over pressure conditions. My tin of WW2 4831, the powder does not smell. The interior of the can was dusty, which is not a good sign, but as you can see from the pictures, the powder "looks good" (except for the case corrosion) . From what I have read, chemical stability tests require gas chromatography, and ballistic stability requires a pressure gauge, to see if the pressure curve has shifted, and the pressure has increased.

NH30lRa.jpg

I have neither, so all I can do is sniff and look. Which is not as exact as laboratory techniques, nor will human senses catch powder problems early.

I am going to state, shoot your powder up before it is 20 years old. Shoot up old stuff first, and plan to shoot up your stocks so nothing on your shelf is older than 20 years. And don't pay full price for powders older than 20 years, in fact, might be better to not buy them. And never buy military pulldown powders. The military tries to remove its propellants when it still has a shelf life of 5 years, that way it can remove the stuff before it auto combusts in the case, or detonates at the demilling facility. I have poured out kegs and hundreds of dollars of pulldown powder because it went bad. I did not know that gunpowder went bad, in fact, had read in the popular press that gunpowder is immortal. Don't believe anything the seller tell you, it is either wishful thinking, because they don't know. Or they know, and are counting on you to trade your cow for magic beans.

I continue to debate those who believe that gunpowder is immortal, or that old gunpowder gets "weaker" in time. Maybe the energy content drops, but the burn rate of deteriorated gunpowder will spike and cause a detonation. Shoot enough old ammunition and you will get the occasional surprise!

bKnKX9p.jpg
 
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I've got Dupont 4831 in #1 lb. cans which are marked $2.85 full retail price as I purchased them for a sporting goods store . Actually a Military collector's Gun shop . So powder is 1968 - 72 ,Era is MY guess and it's just fine . I've got WWl ammo that is also JUST Fine ,with NO outward signs of corrosion but most certainly have corrosive primers .

MY take on photos of corrosion inside those cases in the photos by Slamfire to be ,perhaps excessive humidity or stored in hot humid conditions . The powder is still extruded and Not crumbly ,so I suspect another culprit with regards to corrosion ,rather than the powder itself .
I've also got a few cases of German 8X57 still inside Leaded Tin cans , in their original wood crates from WWll . Along with Turkish 1947 8X57 and Not a single one shows any signs of corrosion ,Yet Primers most certainly are corrosive . Proper Storage is all I can say .
 
i cant speak for powder but i recently shot a box of rounds that were loaded in 87. no problems from any of them. single hole groups.
Long term handloads can be their own animal. Case tarnishing that exponentiates over time, fingerprints that become their own mineroligical formation in colors brown, black and green. The more meticulous with cleaning and handling the better off.
I try not to load long term ones, but definitely have some jacketed hunting loads that are over 12 years old. They're doing OK
 
Using powder that is probably 40+ years old

Any suggestions or comments on my options
https://www.thehighroad.org/index.p...-and-discussions.778197/page-11#post-12480191

HOW TO CHECK SMOKELESS POWDER FOR DETERIORATION - Although modern smokeless powders contain stabilizers and are basically free from deterioration under proper storage conditions, safe practices require a recognition of the signs of deterioration and its possible effects.

Deteriorating smokeless powders produce an acidic odor and may produce a reddish brown fume. (Don’t confuse this with common solvent odors such as alcohol, ether and acetone.) Powder deterioration can be checked by opening the cap on the container and smelling the contents. Powder undergoing deterioration has an irritating acidic odor.

Dispose of deteriorating smokeless powders immediately. Check to make certain that powder is not exposed to extreme heat as this may cause deterioration. Such exposure produces an acidity which accelerates further reaction and has been known, because of the heat generated by the reaction, to cause spontaneous combustion.​
 
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