CarnoSyn® (Beta-Alanine)

Evidence Level
Limited
8 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

CarnoSyn is the beta-alanine ingredient sold by Natural Alternatives International (NAI), which also makes SR CarnoSyn, a sustained-release tablet. The molecule is the same as any beta-alanine. Muscle uses it to make carnosine, a buffer against the acid that builds up in hard exercise. Many of the founding beta-alanine trials used CarnoSyn: it raised muscle carnosine and, in small placebo-controlled trials, improved high-intensity cycling capacity, fatigue thresholds in adults over 55, and some combat tasks in soldiers, while other tests in the same trials did not change. Results for thinking skills were inconsistent. Most CarnoSyn trials were supplied, supported or funded by NAI, and a lead researcher is a named inventor on NAI beta-alanine patents. Skin tingling is the main side effect; in one study of a slow-release tablet not named by brand, blood levels peaked lower and later.

Studied Dose Regular CarnoSyn: 2.4 to 6.4 g a day split into doses of 400 to 800 mg, for 4 weeks to 90 days. SR CarnoSyn or other NAI sustained-release tablets: 2.4 to 6.4 g a day, usually with meals, for 4 to 24 weeks. The ISSN advises 4 to 6 g a day for at least 2 to 4 weeks.
Active Compound Beta-alanine, the building block that limits how much carnosine muscle can make. CarnoSyn is NAI's beta-alanine, used as capsules or powder in the early trials; SR CarnoSyn is NAI's sustained-release tablet form.

Benefits

High-intensity exercise capacity in cycling tests

In a trial of 13 men on CarnoSyn and 12 matched placebo controls, 4 weeks raised total work done in a cycling test at 110% of maximum power by 13.0%, with a further 3.2% after 10 weeks, while the placebo group did not change. The gain followed the rise in muscle carnosine. The trial was small and run by researchers with NAI ties.

Muscle carnosine loading

CarnoSyn at 3.2 or 6.4 g a day for 4 weeks raised thigh muscle carnosine by about 42% and 64%, and 10 weeks raised it by about 80%. In adults aged 60 to 80, sustained-release tablets at 3.2 g a day for 12 weeks raised calf carnosine by 85.4% versus 7.2% on placebo. Carnosine is a marker, not a performance result.

Exercise capacity and fatigue threshold in adults over 55

Two small placebo-controlled trials found gains: 90 days of 2.4 g a day raised the cycling workload reached before muscle fatigue by 28.6% in a trial of 26 adults aged 55 to 92 (12 on beta-alanine), and 12 weeks of sustained-release tablets lengthened time to exhaustion in 18 adults aged 60 to 80. A 100-person trial found no difference from placebo in grip strength or sit-to-stand.

Power and combat task performance in soldiers

In two 4-week trials of 6 g a day of sustained-release tablets in elite combat soldiers, the CarnoSyn groups showed higher peak jump power, more shots on target and a faster 50 m casualty carry than placebo. Run times, sprints and, in the second trial, marksmanship did not differ. Each trial had about 20 soldiers.

Cognitive test scores in soldiers and older adults

In one trial of 18 soldiers, serial subtraction scores were better than placebo after 30 days, but a trial of 20 soldiers and a trial of 19 cyclists found no effect on cognitive tests. In 100 older adults, overall cognitive screening scores did not differ from placebo, though people with lower starting scores improved more.

Mechanism of action

1

Building muscle carnosine

Muscle makes carnosine from beta-alanine and histidine, and beta-alanine is the scarce ingredient. Taking it daily raises muscle carnosine over weeks, in both type I and type IIa fibers, which is why the trials ran for at least 4 weeks rather than testing single doses.

2

Acid buffering during hard efforts

Carnosine soaks up hydrogen ions inside muscle, slowing the fall in pH during intense exercise. This is the proposed reason the CarnoSyn trials found gains in efforts that end in fatigue, such as cycling to exhaustion, rather than in short single sprints.

3

Sustained-release delivery

SR CarnoSyn is a sustained-release tablet form. In a study of slow-release beta-alanine tablets whose brand was not named, the blood peak was lower and later than with a pure solution, total absorption was the same, less was lost in urine, and tingling did not differ from placebo. Tingling tracked blood levels, so a lower peak is the likely reason.

Clinical trials

1
CarnoSyn 3.2 or 6.4 g a Day and Muscle Carnosine
PubMed

Absorption and supplementation study: single doses of 10, 20 and 40 mg/kg of CarnoSyn (named in the abstract) or chicken broth, then 3.2 or 6.4 g a day of beta-alanine in 400 or 800 mg doses, or L-carnosine, for 4 weeks, with muscle biopsies; co-authored by John Wise, described in a later paper as a former NAI employee (Harris et al. 2006, Amino Acids)

Healthy adult volunteers; the abstract does not give the number per group.

Blood beta-alanine peaked and returned to baseline within 2 hours, with under 5% lost in urine. Four weeks raised muscle carnosine by 42.1% (3.2 g) and 64.2% (6.4 g). Plasma taurine rose without extra loss in urine. Muscle carnosine is a marker; no performance test was reported.

2
CarnoSyn for 4 and 10 Weeks: Cycling Capacity
PubMed

Placebo-controlled trial of CarnoSyn (named in the abstract) for 4 weeks, 8 participants continuing to 10 weeks, with muscle biopsies and a cycling capacity test at 110% of maximum power; funding not stated in the abstract; co-authors include Roger Harris, who later disclosed NAI research grants and NAI patents, and John Wise, later described as a former NAI employee (Hill et al. 2007, Amino Acids)

25 participants: 13 men on beta-alanine and 12 matched placebo controls.

Muscle carnosine rose 58.8% at 4 weeks and 80.1% at 10 weeks, with no rise on placebo, and muscle taurine did not change. Total work done rose 13.0% at 4 weeks and a further 3.2% at 10 weeks, while it did not change in the placebo group. Small groups, and only a subset in each group had muscle biopsies.

3
CarnoSyn 2.4 g a Day for 90 Days in Adults Aged 55 to 92
PubMed

Double-blind randomized placebo-controlled trial: 800 mg CarnoSyn capsules three times a day versus microcrystalline cellulose for 90 days; NAI donated the CarnoSyn and placebo; Roger Harris is a co-author (Stout et al. 2008, J Int Soc Sports Nutr)

26 older adults (9 men, 17 women), average age 72.8; 12 on beta-alanine, 14 on placebo.

Physical working capacity at the fatigue threshold, a cycling workload measure, showed a group by time interaction (p = 0.007): it rose 28.6% on CarnoSyn and did not change on placebo. 67% of the CarnoSyn group improved versus 21.5% on placebo. No other outcomes were reported.

4
SR CarnoSyn 3.2 g a Day for 12 Weeks in Adults Aged 60 to 80
PubMed

Double-blind randomized placebo-controlled trial: two 800 mg sustained-release CarnoSyn tablets twice a day versus maltodextrin for 12 weeks; NAI partly sponsored the study and supplied the tablets, with state research foundation support; John Wise is a former NAI employee and NAI consultant, and Roger Harris is a named inventor on NAI patents (del Favero et al. 2012, Amino Acids)

18 healthy adults aged 60 to 80: 12 on beta-alanine and 6 on placebo.

Calf muscle carnosine rose 85.4% versus 7.2% on placebo (p = 0.004). Time to exhaustion in a constant-load test rose 36.5% versus 8.6% (p = 0.05), and in an incremental test 12.2% versus 0.1% (p = 0.04). The carnosine rise correlated with the gains. Timed-stands, timed up-and-go and quality of life did not differ, and no side effects were reported. A very small placebo group.

5
SR CarnoSyn 6 g a Day for 28 Days in Combat Soldiers
PubMed

Randomized placebo-controlled trial: sustained-release CarnoSyn tablets, 2 g (two tablets) three times a day, versus rice powder during advanced military training; CarnoSyn obtained from NAI, which the authors thank for supporting the study; the lead author later disclosed past NAI consulting (Hoffman et al. 2014, J Int Soc Sports Nutr)

20 soldiers from an elite combat unit, average age 20.

Peak jump power (p = 0.034), shots on target (8.2 versus 6.5, p = 0.012) and target engagement speed (p = 0.039) were better than placebo. The 4 km run (p = 0.597) and serial subtraction, a cognitive test (p = 0.844), did not differ. Four soldiers had isolated episodes of tingling, each after taking 2 to 3 doses at once.

6
SR CarnoSyn 6 g a Day for 30 Days: Carnosine and Soldier Tasks
PubMed

Randomized placebo-controlled trial: sustained-release CarnoSyn tablets, 2 g (two tablets) three times a day, versus rice powder, with muscle and brain carnosine measured by magnetic resonance spectroscopy; CarnoSyn obtained from NAI, which the authors thank for support; the lead author later disclosed past NAI consulting (Hoffman et al. 2015, Amino Acids)

18 soldiers from an elite combat unit, average age 19.9.

Muscle carnosine rose more than on placebo (p = 0.048); brain carnosine did not change. The 50 m casualty carry (p = 0.044) and serial subtraction scores (p = 0.022) improved more than placebo. The 2.5 km run, 1 minute sprint, repeated sprints and marksmanship did not differ.

7
NAI Sustained-Release Beta-Alanine 2.4 g a Day in 100 Older Adults
PubMed

Double-blind randomized placebo-controlled trial: sustained-release beta-alanine tablets with meals, 2.4 g a day for 10 weeks; tablets provided by NAI, which also funded the research; the paper declares no conflict of interest, but the senior author disclosed in a separate 2023 review that he has previously consulted for NAI (Ostfeld et al. 2023, Nutrients)

100 older adults, average age 70.6; 79 completed (38 beta-alanine, 41 placebo).

The main cognitive screening score (MoCA) did not differ between groups (p = 0.19). In a subgroup with starting scores of 26 or less, MoCA improved more than placebo (interaction p = 0.042). Stroop test results, mood, anxiety, grip strength and sit-to-stand did not differ; depression scale scores fell on beta-alanine only. No adverse events were reported.

8
SR CarnoSyn 6.4 g a Day for 24 Weeks: Safety
PubMed

Placebo-controlled trial: 6.4 g a day of sustained-release CarnoSyn (named in the abstract) or maltodextrin for 24 weeks, with muscle biopsies at 0, 12 and 24 weeks and blood tests every 4 weeks; Roger Harris is a co-author (Saunders et al. 2020, Eur J Nutr)

25 healthy men, average age 27: 16 on beta-alanine and 9 on placebo.

Muscle taurine showed no time or group by time effect (values were lower overall in the placebo group). Kidney, liver and muscle blood markers showed no treatment, time or interaction effect, and no participant reported side effects over 24 weeks. A small trial in men only.

Side effects and drug interactions

Common Potential side effects

Tingling (paresthesia) of the skin is the only side effect the ISSN position stand reports for beta-alanine, mostly after single doses above about 800 mg of a regular, non-sustained-release form. It is not known to be harmful.
Sustained-release tablets: in a 24-week trial of 6.4 g a day of SR CarnoSyn, no participant reported side effects, and in a 28-day trial of 6 g a day, tingling occurred only in four soldiers who took 2 to 3 doses at once. In other trials whose abstracts do not name the brand, slow-release tablets caused tingling no different from placebo.
Taurine: beta-alanine and taurine share a transporter into muscle. Muscle taurine did not change after 10 weeks of CarnoSyn or 24 weeks of SR CarnoSyn, and kidney, liver and muscle blood markers did not change over 24 weeks.
Long-term use beyond 24 weeks has not been tested in the CarnoSyn trials cited here, and we found no human data in pregnancy or breastfeeding.

Important Drug interactions

No drug interactions were reported in the CarnoSyn trials cited on this page. If you take prescription medication, check with a pharmacist or doctor first.

Frequently asked questions about CarnoSyn® (Beta-Alanine)

What is CarnoSyn?

CarnoSyn is a branded beta-alanine sold by Natural Alternatives International. SR CarnoSyn is its sustained-release tablet. The molecule is the same as other beta-alanine; what sets the brand apart is that many of the original beta-alanine trials used it.

How is SR CarnoSyn different from regular CarnoSyn?

SR CarnoSyn is a sustained-release tablet. In a study of slow-release beta-alanine tablets whose brand was not named, the blood peak was lower and later than with a pure solution, and tingling did not differ from placebo. In a 24-week trial of 6.4 g a day of SR CarnoSyn, no participant reported side effects. Both forms raise muscle carnosine.

How much CarnoSyn was used in studies?

Trials used 2.4 to 6.4 g a day for 4 to 24 weeks, with regular CarnoSyn split into 400 to 800 mg doses and SR CarnoSyn tablets usually taken with meals. Because it works by building muscle carnosine over weeks, taking it every day matters more than timing.

Who funded the CarnoSyn research?

Most CarnoSyn trials were supplied, supported or partly funded by NAI. A leading beta-alanine researcher on many of them is a named inventor on NAI patents and has consulted for NAI, and another co-author is a former NAI employee.

Does CarnoSyn help memory or thinking?

It has not been shown. One trial in 18 soldiers found better serial subtraction scores than placebo, but trials in 20 soldiers and 19 cyclists found no effect. In 100 older adults, overall cognitive screening scores did not differ from placebo; only a subgroup with lower starting scores improved more.

What is CarnoSyn used for?

CarnoSyn is researched primarily for Athletic Performance. In a trial of 13 men on CarnoSyn and 12 matched placebo controls, 4 weeks raised total work done in a cycling test at 110% of maximum power by 13.0%, with a further 3.2% after 10 weeks, while the placebo group did not change.

Is CarnoSyn safe, and does it have side effects?

Side effects and cautions reported for CarnoSyn include: Tingling (paresthesia) of the skin is the only side effect the ISSN position stand reports for beta-alanine, mostly after single doses above about 800 mg of a regular, non-sustained-release form. It is not known to be harmful. Sustained-release tablets: in a 24-week trial of 6. It may also interact with some medications. CarnoSyn is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does CarnoSyn interact with any medications?

Possible interactions include: No drug interactions were reported in the CarnoSyn trials cited on this page. If you take prescription medication, check with a pharmacist or doctor first. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for CarnoSyn?

NutraSmarts rates the evidence for CarnoSyn as Limited (2 out of 5). It is backed by 8 study summaries and 16 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(16 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Harris RC, Tallon MJ, Dunnett M, Boobis L, Coakley J, Kim HJ, Fallowfield JL, Hill CA, Sale C, Wise JA. The absorption of orally supplied beta-alanine and its effect on muscle carnosine synthesis in human vastus lateralis. Amino Acids. 2006;30(3):279-89. doi: 10.1007/s00726-006-0299-9.PubMedUsed to support: Absorption and loading study using CarnoSyn (named in the abstract). Blood beta-alanine peaked and returned to baseline within 2 hours, under 5% was lost in urine, plasma taurine rose without extra urinary loss, and 3.2 or 6.4 g a day for 4 weeks raised muscle carnosine by 42.1% and 64.2%. Co-author John Wise was later described as a former NAI employee.
  2. Hill CA, Harris RC, Kim HJ, Harris BD, Sale C, Boobis LH, Kim CK, Wise JA. Influence of beta-alanine supplementation on skeletal muscle carnosine concentrations and high intensity cycling capacity. Amino Acids. 2007;32(2):225-33. doi: 10.1007/s00726-006-0364-4.PubMedUsed to support: CarnoSyn (named in the abstract) for 4 weeks (13 men) and 10 weeks (8 men) versus 12 placebo controls. Muscle carnosine rose 58.8% and 80.1%, taurine did not change, and total work in a cycling test at 110% of maximum power rose 13.0% at 4 weeks and a further 3.2% at 10 weeks, while placebo did not change.
  3. Stout JR, Cramer JT, Zoeller RF, Torok D, Costa P, Hoffman JR, Harris RC, O'Kroy J. Effects of beta-alanine supplementation on the onset of neuromuscular fatigue and ventilatory threshold in women. Amino Acids. 2007;32(3):381-6. doi: 10.1007/s00726-006-0474-z.PubMedUsed to support: Randomized trial of CarnoSyn (named in the abstract) for 28 days in 22 women aged about 27. Ventilatory threshold, physical working capacity at the fatigue threshold and time to exhaustion rose 13.9%, 12.6% and 2.5% within the beta-alanine group, with no change on placebo; maximal oxygen uptake did not change. The abstract reports within-group changes.
  4. Stout JR, Graves BS, Smith AE, Hartman MJ, Cramer JT, Beck TW, Harris RC. The effect of beta-alanine supplementation on neuromuscular fatigue in elderly (55-92 Years): a double-blind randomized study. J Int Soc Sports Nutr. 2008;5:21. doi: 10.1186/1550-2783-5-21.PubMedUsed to support: Double-blind randomized trial in 26 adults aged 55 to 92: 800 mg CarnoSyn capsules three times a day for 90 days, donated by NAI. Physical working capacity at the fatigue threshold showed a group by time interaction (p = 0.007), rising 28.6% on beta-alanine with no change on placebo (full text, PMC2585553).
  5. del Favero S, Roschel H, Solis MY, Hayashi AP, Artioli GG, Otaduy MC, Benatti FB, Harris RC, Wise JA, Leite CC, Pereira RM, de Sá-Pinto AL, Lancha-Junior AH, Gualano B. Beta-alanine (Carnosyn™) supplementation in elderly subjects (60-80 years): effects on muscle carnosine content and physical capacity. Amino Acids. 2012;43(1):49-56. doi: 10.1007/s00726-011-1190-x.PubMedUsed to support: Randomized trial of sustained-release CarnoSyn tablets, 3.2 g a day for 12 weeks, in 18 adults aged 60 to 80. Muscle carnosine rose 85.4% versus 7.2% on placebo, and time to exhaustion improved in constant-load and incremental tests. Full text (PMC3374124): NAI partly sponsored the study and supplied the tablets; John Wise is a former NAI employee and NAI consultant; Roger Harris held NAI research grants, is a named inventor on NAI patents for raising muscle carnosine with beta-alanine, and is an unpaid NAI consultant.
  6. Hoffman JR, Landau G, Stout JR, Dabora M, Moran DS, Sharvit N, Hoffman MW, Ben Moshe Y, McCormack WP, Hirschhorn G, Ostfeld I. β-alanine supplementation improves tactical performance but not cognitive function in combat soldiers. J Int Soc Sports Nutr. 2014;11(1):15. doi: 10.1186/1550-2783-11-15.PubMedUsed to support: Randomized trial in 20 combat soldiers: 6 g a day of sustained-release CarnoSyn obtained from NAI for 28 days improved peak jump power, shots on target and target engagement speed versus placebo, but not 4 km run time or serial subtraction scores. Full text (PMC3983672): four soldiers had isolated tingling after combining doses; the authors thank NAI for support and declare no competing interests.
  7. Hoffman JR, Landau G, Stout JR, Hoffman MW, Shavit N, Rosen P, Moran DS, Fukuda DH, Shelef I, Carmom E, Ostfeld I. β-Alanine ingestion increases muscle carnosine content and combat specific performance in soldiers. Amino Acids. 2015;47(3):627-36. doi: 10.1007/s00726-014-1896-7.PubMedUsed to support: Randomized trial in 18 combat soldiers: sustained-release CarnoSyn from NAI, 6 g a day for 30 days, raised muscle carnosine more than placebo but not brain carnosine, and improved 50 m casualty carry time and serial subtraction scores versus placebo, but not run, sprint or marksmanship results. The authors thank NAI for support (full text, PMC4326648).
  8. Ostfeld I, Ben-Zeev T, Zamir A, Levi C, Gepner Y, Springer S, Hoffman JR. Role of β-Alanine Supplementation on Cognitive Function, Mood, and Physical Function in Older Adults; Double-Blind Randomized Controlled Study. Nutrients. 2023;15(4):923. doi: 10.3390/nu15040923.PubMedUsed to support: Double-blind randomized trial in 100 older adults: 2.4 g a day of sustained-release beta-alanine tablets supplied by NAI for 10 weeks; funded by NAI. MoCA scores did not differ between groups overall (p = 0.19) but improved more on beta-alanine in those with starting scores of 26 or less; Stroop, mood, anxiety, grip strength and sit-to-stand did not differ (full text, PMC9960300).
  9. Saunders B, Franchi M, de Oliveira LF, da Eira Silva V, da Silva RP, de Salles Painelli V, Costa LAR, Sale C, Harris RC, Roschel H, Artioli GG, Gualano B. 24-Week β-alanine ingestion does not affect muscle taurine or clinical blood parameters in healthy males. Eur J Nutr. 2020;59(1):57-65. doi: 10.1007/s00394-018-1881-0.PubMedUsed to support: Placebo-controlled trial in 25 healthy men: 6.4 g a day of sustained-release CarnoSyn (named in the abstract) for 24 weeks did not change muscle taurine over time or relative to placebo, had no effect on kidney, liver or muscle blood markers, and caused no self-reported side effects.
  10. Solis MY, Cooper S, Hobson RM, Artioli GG, Otaduy MC, Roschel H, Robertson J, Martin D, S Painelli V, Harris RC, Gualano B, Sale C. Effects of beta-alanine supplementation on brain homocarnosine/carnosine signal and cognitive function: an exploratory study. PLoS One. 2015;10(4):e0123857. doi: 10.1371/journal.pone.0123857.PubMedUsed to support: Two exploratory studies: 6.4 g a day of beta-alanine for 28 days did not change brain homocarnosine/carnosine signal in 14 vegetarians and omnivores, and in 19 trained male cyclists (Study 2) did not affect Stroop, Sternberg or RVIP cognitive test results at rest or after exercise. Per the full text (PMC4397072), both studies used CarnoSyn SR tablets, listed in the methods as from Compound Solutions Inc., and the competing-interests statement says NAI provided the supplements for Study 2. Roger Harris disclosed NAI grants, NAI patents and NAI consulting.
  11. Hobson RM, Saunders B, Ball G, Harris RC, Sale C. Effects of β-alanine supplementation on exercise performance: a meta-analysis. Amino Acids. 2012;43(1):25-37. doi: 10.1007/s00726-011-1200-z.PubMedUsed to support: Meta-analysis context, pooling beta-alanine trials of several sources: 15 studies, 360 participants. Beta-alanine improved exercise outcomes more than placebo, mainly exercise capacity, for efforts of 60 to 240 s and over 240 s but not under 60 s, with a median improvement of 2.85%. The full text (PMC3374095) notes that 8 of the 15 studies acknowledged a commercially donated supplement, 3 named the brand and 4 gave no source. It declares no conflicts of interest, although co-author Roger Harris is disclosed elsewhere as a named inventor on NAI patents.
  12. Trexler ET, Smith-Ryan AE, Stout JR, Hoffman JR, Wilborn CD, Sale C, Kreider RB, Jäger R, Earnest CP, Bannock L, Campbell B, Kalman D, Ziegenfuss TN, Antonio J. International society of sports nutrition position stand: Beta-Alanine. J Int Soc Sports Nutr. 2015;12:30. doi: 10.1186/s12970-015-0090-y.PubMedUsed to support: ISSN position stand (not brand specific): 4 to 6 g a day for at least 2 to 4 weeks raises muscle carnosine and improves exercise performance, most in 1 to 4 minute tasks; it attenuates neuromuscular fatigue, particularly in older people; tingling is the only reported side effect and can be reduced with divided 1.6 g doses or a sustained-release form; there are no safety data beyond 1 year (full text, PMC4501114).
  13. Décombaz J, Beaumont M, Vuichoud J, Bouisset F, Stellingwerff T. Effect of slow-release β-alanine tablets on absorption kinetics and paresthesia. Amino Acids. 2012;43(1):67-76. doi: 10.1007/s00726-011-1169-7.PubMedUsed to support: Other product or unconfirmed source: the abstract does not name the slow-release tablet brand. In 11 adults, 1.6 g as slow-release tablets gave a lower peak blood level than a pure solution (82 versus 248 umol/L) with the same total absorption and less urinary loss, and caused tingling no different from placebo.
  14. Varanoske AN, Hoffman JR, Church DD, Coker NA, Baker KM, Dodd SJ, Harris RC, Oliveira LP, Dawson VL, Wang R, Fukuda DH, Stout JR. Comparison of sustained-release and rapid-release β-alanine formulations on changes in skeletal muscle carnosine and histidine content and isometric performance following a muscle-damaging protocol. Amino Acids. 2019;51(1):49-60. doi: 10.1007/s00726-018-2609-4.PubMedUsed to support: Unconfirmed source: the abstract does not name the brand. In 39 recreationally active adults, 6 g a day for 28 days of a sustained-release formulation raised muscle carnosine 50.1% (significant versus placebo) and a rapid-release formulation 37.9% (not significant versus placebo); both reduced fatigue in isometric contractions, and tingling was more frequent with rapid release, while sustained release did not differ from placebo.
  15. McCormack WP, Stout JR, Emerson NS, Scanlon TC, Warren AM, Wells AJ, Gonzalez AM, Mangine GT, Robinson EH 4th, Fragala MS, Hoffman JR. Oral nutritional supplement fortified with beta-alanine improves physical working capacity in older adults: a randomized, placebo-controlled study. Exp Gerontol. 2013;48(9):933-9. doi: 10.1016/j.exger.2013.06.003.PubMedUsed to support: Other product or unconfirmed source: the abstract does not name the beta-alanine supplier. In 60 adults aged about 71, an oral nutritional drink with 800 or 1200 mg of beta-alanine twice a day for 12 weeks raised physical working capacity at the fatigue threshold (17.8% and 13.6%) more than the drink alone (minus 6.3%); body composition and grip strength did not change; 44 completed.
  16. Ostfeld I, Hoffman JR. The Effect of β-Alanine Supplementation on Performance, Cognitive Function and Resiliency in Soldiers. Nutrients. 2023;15(4):1039. doi: 10.3390/nu15041039.PubMedUsed to support: Review of beta-alanine in soldiers by two trial authors, cited here for its disclosure: the authors state that they have conducted sponsored supplement research and that Jay Hoffman has previously served as a scientific consultant for NAI. The review calls the evidence on cognitive function inconclusive.