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Fluid Thioglycollate Medium (FTM) | USP <71> Sterility Testing Medium for Aerobic & Anaerobic Bacteria

Fluid Thioglycollate Medium (FTM) | USP <71> Sterility Testing Medium for Aerobic & Anaerobic Bacteria

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Fluid Thioglycollate Medium (FTM)
Multi-Purpose Enriched Reducing Medium for Aerobic and Anaerobic Cultivation
Catalogue No: AS-1233
USP <71> BP 2023 EP 2.6.1 FDA-BAM ISO 21149 Anaerobic Culture Australian Made
Overview

Fluid Thioglycollate Medium (FTM) is a multi-purpose enriched reducing liquid medium for the simultaneous cultivation of obligate aerobes, microaerophiles, facultative anaerobes, and obligate anaerobes. Sodium thioglycollate and L-cystine create a self-generating oxygen gradient — aerobic at the surface, anaerobic at the bottom — without requiring anaerobic jars.

Resazurin provides visual monitoring of oxygen penetration (pink = aerobic; colourless = anaerobic). The semi-solid agar (0.75 g/L) maintains fluid consistency for easy pipetting while retarding convection to preserve the gradient. Validated per USP <71>, BP 2023, EP 2.6.1, FDA-BAM, APHA, and ISO 21149.

FTM vs Brewer Modified — Key Differences
Parameter FTM (AS-1233) Brewer Modified (AS-1364)
Dextrose 5.5 g/L 2.5 g/L
Agar (semi-solid) 0.75 g/L 0.5 g/L
NaCl 2.5 g/L 5.0 g/L
Pharmacopoeial standard USP <71>, BP, EP 2.6.1 USP <71>, BP, EP 2.6.1
Best use Pharmaceutical sterility testing; clinical blood cultures Routine anaerobic enrichment; Brewer protocols
Typical Composition (per litre)
Ingredient Amount (g/L) Function
Pancreatic Digest of Casein 15.0 Nitrogen, peptides, amino acids
Yeast Extract 5.0 Vitamins, growth factors
Dextrose (D-Glucose) 5.5 Carbon/energy source, mild reductant
L-Cystine 0.5 Secondary reducing agent, sulfur source
Sodium Chloride 2.5 Osmotic balance
Sodium Thioglycollate 0.5 Primary reducing agent — O₂ scavenger
Agar (semi-solid) 0.75 Oxygen gradient maintenance
Resazurin (sodium salt) 0.001 Redox indicator
Final pH (25 °C) 7.1 ± 0.2
Applications
  • Pharmaceutical sterility testing: USP <71>, BP 2023, EP 2.6.1 — parenterals, ophthalmics, biologics, medical devices
  • Clinical microbiology: Blood culture enrichment, anaerobe isolation from wounds/abscesses (C. perfringens, B. fragilis)
  • Food & cosmetics: Total viable count — ISO 21149 (cosmetics), APHA (dairy, food), FDA-BAM
  • Environmental: Anaerobe screening from soil, sediment, water samples
Preparation
  1. Suspend 29.25 g in 1 litre of purified water. Heat with agitation to near boiling until dissolved. Do not overheat.
  2. Dispense into tubes or bottles (10–20 mL per tube for sterility testing).
  3. Autoclave at 121 °C for 15 minutes with caps loosened.
  4. Cool to ~25 °C and tighten caps.
  5. If >30% of medium turns pink: reheat in boiling water bath for 4 minutes. Cool rapidly. Do this once only.
  6. Prepared medium: light straw-coloured, clear, fluid, without precipitate.
CRITICAL — Pharmaceutical sterility testing: Use only medium that is colourless or at most faintly pink (≤30% depth). Discard if >30% pink. Follow full pharmacopoeial preparation and validation requirements (USP <71>, BP, EP 2.6.1).
Growth Pattern Interpretation
Observation Organism Type Examples
Turbidity throughout Facultative anaerobes Staphylococcus, Enterobacteriaceae
Turbidity at bottom only Obligate anaerobes Clostridium, Bacteroides, Fusobacterium
Pellicle or surface turbidity Obligate aerobes Pseudomonas, Bacillus
Mid-zone turbidity Microaerophiles Campylobacter, Helicobacter
No growth after 14 days (pharma) Sterile — PASS Document per pharmacopoeia
Any growth after 14 days (pharma) Not sterile — FAIL Investigate and report
Storage
Dehydrated powder 10–30 °C, tightly sealed, dry, protected from light and humidity
Shelf life (powder) 3 years from manufacture date
Prepared broth 15–30 °C, sealed containers, use within 4 weeks
If refrigerated 2–8 °C — warm to room temperature before use
Discard if Pink >30%, turbid before inoculation, precipitate, or evaporated
For Laboratory Use Only. Not for human, veterinary, food, or pharmaceutical consumption. Handle inoculated medium at BSL-2. Autoclave all waste before disposal.
For laboratory use only. AuSaMicS Pty Ltd | ABN 56 676 640 467 | www.ausamics.com.au
Product Identification
Product Name Fluid Thioglycollate Medium (FTM)
Catalogue Number AS-1233
HS Code 3821.00.00
Pharmacopoeial Equivalents USP <71>, BP 2023, EP 2.6.1 — Fluid Thioglycollate Medium
Regulatory Compliance FDA-BAM, APHA, ISO 21149
Also known as FTM, Thioglycollate Broth, Fluid Thioglycollate Broth, THIO
Related product Thioglycollate Medium Brewer Modified (AS-1364)
Physical & Chemical Specifications
pH (prepared, 25 °C) 7.1 ± 0.2
Moisture (loss on drying) ≤ 5.0%
Agar concentration 0.75 g/L (semi-solid — fluid, not gel)
Dextrose concentration 5.5 g/L
Resazurin indicator 0.001 g/L — colourless (reduced) ↔ pink (oxidised)
Reducing system Dual: sodium thioglycollate (0.5 g/L) + L-cystine (0.5 g/L)
Total solids ~29.25 g/L
Performance Specifications (Pharmacopoeial)
Organism ATCC No. Expected Result Ref.
Clostridium sporogenes 11437 Growth — lower zone turbidity USP <71> / EP 2.6.1
Staphylococcus aureus 6538 Growth throughout USP <71> / EP 2.6.1
Pseudomonas aeruginosa 9027 Growth at surface USP <71> / EP 2.6.1
Bacillus subtilis 6633 Growth at/near surface USP <71> / EP 2.6.1
Candida albicans 10231 Growth throughout (20–25 °C) USP <71>
Aspergillus brasiliensis 16404 Surface growth / pellicle (20–25 °C) USP <71>
Bacteroides fragilis 25285 Growth — lower zone EP / Clinical
Clostridium perfringens 13124 Growth — lower zone FDA-BAM / EP
Key Limitations
  • Pink zone must not exceed 30% of tube depth before inoculation
  • For pharmacopoeial sterility testing — prepare and validate per applicable pharmacopoeia
  • Do not overheat — degrades reducing agents and dextrose
  • Reheat only once if pink >30% — repeated heating degrades medium
  • Not suitable for strict aerobe isolation without surface inoculation technique
Version 1.0 — March 2026. AuSaMicS Pty Ltd | ABN 56 676 640 467 | www.ausamics.com.au
GHS Classification: Mixture not classified as hazardous at use concentration (AU WHS Regulations 2011) | Note: Sodium thioglycollate — H302/H311/H331 at high concentration; negligible risk at 0.5 g/L working level | ADG: Not regulated | BSL-2 precautions for inoculated medium.
Section 1 — Identification
Product Name Fluid Thioglycollate Medium (FTM)
Catalogue Number AS-1233
Intended Use Multi-purpose enriched reducing medium — aerobic/anaerobic cultivation and pharmaceutical sterility testing. Laboratory use only.
Supplier AuSaMicS Pty Ltd | 31 Longview CT, Thomastown VIC 3074
ABN 56 676 640 467
Emergency Phone +61 412 520 598 | Poisons Information: 13 11 26 (24 hr)
Email support@ausamics.com.au
Section 3 — Composition
Component CAS % Classification
Pancreatic Digest of Casein 73049-73-7 ~51.3% Not classified
Yeast Extract 8013-01-2 ~17.1% Not classified
Dextrose 50-99-7 ~18.8% Not classified
L-Cystine 56-89-3 ~1.7% Not classified
Sodium Chloride 7647-14-5 ~8.5% Not classified
Sodium Thioglycollate 367-51-1 ~1.7% H302, H311, H331 (at high conc.)
Agar 9002-18-0 ~2.6% Not classified
Resazurin 62758-13-8 <0.01% Not classified at this level
Sections 4–8 — First Aid, Handling & PPE
Topic Guidance
Inhalation Remove to fresh air. Seek medical advice if symptoms persist.
Skin Contact Wash with soap and water ≥15 minutes. Sodium thioglycollate — potential sensitiser with repeated exposure.
Eye Contact Flush with copious water ≥15 minutes. Seek medical attention.
Ingestion Do not induce vomiting. Rinse mouth. Seek medical advice. Inform physician of sodium thioglycollate content.
Inoculated spill BSL-2. Universal Precautions. Disinfect with 1% sodium hypochlorite. Autoclave all contaminated material.
PPE Nitrile gloves, safety glasses/goggles, lab coat. BSC for clinical/inoculated work.
Section 13 — Disposal

Uninoculated: Chemical waste per local EPA regulations. Neutralise reducing agents before small-quantity drain disposal.

Inoculated / clinical medium: Autoclave at 121 °C for 30 minutes minimum. Treat as BSL-2 biological waste per institutional and local biosafety requirements.

Section 15 — Regulatory
WHS Regulations 2011 Mixture not classified as hazardous at use concentration
Pharmacopoeial use USP <71>, BP 2023, EP 2.6.1 validated medium
Transport (ADG/IATA) Not classified as dangerous goods
Prepared per Australian WHS Regulations and GHS 7th Edition. Version 1.0 — March 2026. AuSaMicS Pty Ltd | ABN 56 676 640 467 | www.ausamics.com.au
Product Information
Product Name Fluid Thioglycollate Medium (FTM)
Catalogue Number AS-1233
Pharmacopoeial Ref. USP <71>, BP 2023, EP 2.6.1 | FDA-BAM | ISO 21149
Lot / Batch Number Contact us for batch-specific COA
Manufacturing Date Available on request
Expiry Date 3 years from manufacture
Storage Conditions 10–30 °C, tightly sealed, dry; prepared: 15–30 °C, use within 4 weeks
Specification & Test Results
Test Specification Typical Result Status
Appearance (powder) Cream to light beige powder Complies ✓ PASS
Colour (prepared) Light straw/clear; pink ≤30% surface Complies ✓ PASS
pH (prepared, 25 °C) 7.1 ± 0.2 Complies ✓ PASS
Moisture (loss on drying) ≤ 5.0% Complies ✓ PASS
Solubility Completely soluble — no precipitate Complies ✓ PASS
Sterility (prepared) No microbial growth Complies ✓ PASS
Resazurin indicator Colourless (reduced) / pink (oxidised) Complies ✓ PASS
C. sporogenes ATCC 11437 Growth — lower zone Complies ✓ PASS
S. aureus ATCC 6538 Growth throughout Complies ✓ PASS
P. aeruginosa ATCC 9027 Growth at surface Complies ✓ PASS
C. albicans ATCC 10231 Growth throughout (20–25 °C) Complies ✓ PASS
A. brasiliensis ATCC 16404 Surface growth / pellicle Complies ✓ PASS
Oxidation limit Pink zone ≤30% of total depth Complies ✓ PASS
Authorisation
Released by Hassan Salimi
Title Founder and Technical Director
Organisation AuSaMicS Pty Ltd
Need a batch-specific COA?
Contact us with your order number and we will issue a full COA within 1 business day.
support@ausamics.com.au  |  +61 412 520 598
This COA is valid for the batch identified above. Not transferable to other batches. AuSaMicS Pty Ltd | ABN 56 676 640 467 | www.ausamics.com.au

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