Glossary

Short, practical definitions for the vocabulary used in peptide sourcing, analytics and logistics. Each entry links to the guide that covers it in depth.

Analytical & quality

HPLC
High-performance liquid chromatography. Separates components of a sample and reports area percentages at a chosen wavelength; the basis of most peptide purity figures. Read more
Chromatogram
The plotted output of an HPLC run. Look at peak shape, baseline and impurity peaks, not only the main-peak percentage. Read more
Mass spectrometry (MS)
Measures molecular mass to confirm identity. An MS result supports “this is the right molecule”; it does not by itself prove purity. Read more
Sequence
The order of amino acid residues from the N-terminus to the C-terminus, written in one-letter code. Direction, terminal groups and modifications are part of the identity, not decoration. Read more
Residue mass
The mass of an amino acid after it has lost water forming the peptide bond. A peptide's free-acid mass is the sum of residue masses plus one water molecule. Read more
Monoisotopic mass
Mass calculated from the single most abundant isotope of each element. It differs from average mass, and the gap grows with molecule size. Read more
b and y ions
The two backbone fragment series used to read a peptide sequence in tandem MS. A b ion is an N-terminal fragment plus a proton; a y ion is a C-terminal fragment plus water and a proton. Read more
Sequence coverage
The share of backbone positions supported by observed fragment ions in an MS/MS experiment. A high percentage can still hide an unconfirmed stretch in the middle of the sequence. Read more
Isobaric residues
Different residues with the same mass — leucine and isoleucine most notably. Mass alone cannot distinguish them, and standard CID fragmentation usually cannot either. Read more
Stability study
A protocol that measures defined attributes over time at stated storage conditions. Real-time data support a shelf life; accelerated data describe degradation pathways. Read more
Purity vs assay
Purity is the share of the main peak by a given method. Assay is the quantity of the target compound measured against a standard. They are not interchangeable. Read more
Related impurity
A molecule close in structure to the target — a deletion, truncation or oxidation product. Its profile matters more than a single purity number. Read more
Karl Fischer titration
The standard method for water content in a lyophilized cake. Residual moisture affects stability and cake integrity. Read more
Net peptide content
The mass fraction of a powder that is peptide, excluding counter-ion, water and residual salts. Different from HPLC purity. Read more
Fill weight
The total powder mass in a vial. It includes the counter-ion and residual moisture, so it is not the mass of peptide. Read more
Amino-acid analysis (AAA)
Hydrolysis of a sample to free amino acids, followed by separation and quantification. A primary method for peptide content. Read more
Mass balance
Estimating peptide content by subtracting water, counter-ion and residual solvents from 100%. Only as good as the subtracted assays. Read more
Extinction coefficient
The molar absorptivity used to convert an absorbance reading into a concentration (M⁻¹cm⁻¹). For peptides it is estimated from Trp, Tyr and cystine content. Read more
Beer–Lambert law
A = ε·c·l: absorbance is proportional to concentration and path length. It holds only for dilute solutions without scattering. Read more
BCA assay
A colorimetric protein/peptide assay based on copper reduction. Sequence-dependent and incompatible with reducing agents such as DTT. Read more
qNMR
Quantitative nuclear magnetic resonance against an internal standard. A primary concentration method when the compound is soluble and a signal is resolvable. Read more
Reference standard
A lot with an assigned value and a stated uncertainty, characterised by an independent programme and used to calibrate working standards or settle disputes. Read more
Working standard
A lot qualified in-house against a reference standard, used for routine system suitability and calibration. It carries the assigned value forward, and needs its own records. Read more
System suitability
The injections and checks run before a sample sequence to show the system is fit that day: resolution, tailing, repeatability and carryover. Read more
Dwell volume
The liquid volume between the gradient mixer and the column. It delays the programmed gradient, and differences between instruments shift retention on transfer. Read more
End-capping
A treatment that blocks residual silanol groups on a silica column. Fewer free silanols means less tailing for basic peptides at low pH. Read more
ICP-MS
Inductively coupled plasma mass spectrometry. Measures total element concentration at trace levels; sample digestion decides whether the result is complete. Read more
ICH Q3D
The guideline that classifies elemental impurities by toxicity and sets permitted daily exposures. For a research peptide without a dose, it informs limits rather than fixing them. Read more
PDE (permitted daily exposure)
A dose-based limit for an elemental impurity. It cannot be converted to a ppm specification without a defined daily dose. Read more
Speciation
The chemical form of an element — oxidation state or bound species. Total element analysis by ICP-MS does not report speciation. Read more
COA (certificate of analysis)
The lot-specific document stating test methods, results and specification limits. It must reference the batch it belongs to. Read more
Retention sample
Material held back from a lot for later comparison or retest. Ask for it contractually; it is the cheapest dispute tool you have. Read more
Specification
The written set of limits and methods a lot must meet. A product name is not a specification. Read more
OOS (out of specification)
A result outside the agreed limits. The response — rejection, investigation or retest — should be defined before you order. Read more
Preparative HPLC
Chromatography run to recover material rather than to measure it. Overloaded columns trade resolution for throughput, and the fraction cut sets purity and yield together. Read more
Salt conversion
Exchanging the counter-ion associated with a peptide — commonly TFA for acetate — without changing the sequence. Each exchanged site shifts salt mass by roughly 54 Da. Read more
SEC (size-exclusion chromatography)
Separation by hydrodynamic size. Good for stable oligomers; dilution on the column can dissociate weak aggregates. Read more
DLS (dynamic light scattering)
Derives a hydrodynamic radius from scattered-light fluctuations. Intensity-weighted, so a few large species can dominate the result. Read more
AUC (analytical ultracentrifugation)
Sedimentation analysis in a centrifugal field. Resolves species in solution without a column, but is slow and specialist. Read more

Manufacturing

SPPS
Solid-phase peptide synthesis. The peptide is built stepwise on a resin, then cleaved and purified. Scale and resin choice drive impurity profiles. Read more
Resin
The solid support for SPPS. A change of resin lot can shift coupling efficiency and the impurity profile. Read more
Cleavage and deprotection
The step that releases the peptide from the resin and removes side-chain protecting groups. Incomplete cleavage leaves modified by-products. Read more
Purification
Usually preparative HPLC. Gradient and fraction cutting determine which impurities survive into the final lot. Read more
Lyophilization
Freeze-drying. Removes water from the purified solution to give a stable cake; the cycle affects moisture and cake structure. Read more
Counter-ion
The ion paired with the peptide — commonly acetate or TFA. It changes mass, pH and solubility, and should be stated on the specification. Read more
Batch / lot
A single production run with one batch number. Certificates and retention samples attach to the lot, not to the product name. Read more
Scale-up
Moving a synthesis from grams to tens or hundreds of grams. Coupling and purification behaviour change; a successful small run does not guarantee the large one. Read more

Sourcing & commercial

MOQ
Minimum order quantity. Often set per SKU and per packaging format rather than per order. Read more
Tier pricing
Unit price steps tied to quantity. Confirm whether tiers apply per SKU or across a mixed order. Read more
RFQ
Request for quotation. A useful RFQ lists SKU, strength, quantity, destination and documentation requirements. Read more
Incoterms
Standard trade terms (EXW, FOB, CIF, DDP) that allocate cost and risk. Name the term and the place in the contract. Read more
HS code
Customs classification code. The code determines duty and whether an import permit is required at destination. Read more
T/T (telegraphic transfer)
A bank wire payment. Common for first orders; the protection it offers depends on what the payment is conditioned on, not on the transfer itself. Read more
Letter of credit (L/C)
A bank undertaking to pay against compliant documents. It protects both sides only if the document set is written precisely and checked strictly. Read more
Beneficiary
The account holder receiving a payment. It must match the contracting entity; mismatches are the most common sign of payment fraud in this trade. Read more
Escrow
Funds held by a third party and released when agreed milestones are met. Useful for mid-size orders where neither full prepayment nor credit terms is acceptable. Read more
Change control
The contractual process for notifying and approving changes to process, site or specification. Its absence is a common source of silent drift. Read more
OEM
Original equipment manufacturer. Here: supply under the buyer’s brand, with agreed label and documentation. Read more
Private label
A product sold under the buyer’s brand rather than the manufacturer’s. Label rules and registrations differ by market. Read more
Qualification
The pre-order process of checking documentation, samples and references before committing to a supplier. Read more
Dual sourcing
Qualifying a second supplier for a critical SKU to reduce single-source risk. Requires comparable specifications. Read more
Retest date
The date to which a supplier warrants the specification, after which the lot must be re-analysed before use. Not the same as an expiry date. Read more
Safety stock
Inventory held to cover lead-time variability rather than average demand. Scales with the standard deviation of lead time, not with the mean. Read more

Handling & logistics

Lyophilized powder
Freeze-dried peptide, typically a porous cake or powder in a sealed vial. More stable in transit than a solution. Read more
Reconstitution
Dissolving lyophilized peptide in a suitable laboratory solvent. Concentration is calculated from the measured mass, not assumed. Read more
Freeze–thaw cycle
Repeated freezing and thawing of a solution. Aliquot before freezing to limit damage. Read more
Cold chain
Temperature-controlled handling from dispatch to delivery. Required for sensitive material; overkill for many lyophilized lots on short routes. Read more
Phase-change pack
A pack that holds a temperature band during transit. Check it is still within range on arrival. Read more
Desiccant
A moisture absorber included in packaging. It manages humidity, not temperature. Read more
Aggregation
Non-specific clumping of peptide molecules through hydrophobic and charge interactions. It can reduce soluble recovery without changing the certificate. Read more
Self-assembly
Sequence-encoded organisation of peptides into defined structures such as fibrils or gels. A property of the molecule, not a handling error. Read more
Isoelectric point (pI)
The pH at which a peptide carries no net charge and is usually least soluble. Buffer away from it rather than relying on water. Read more
Headspace
The gas volume above the powder in a vial or pouch. Its oxygen and moisture content drive slow degradation; inert-gas flushing reduces it. Read more
Customs hold
Detention of a shipment for inspection or missing documents. Plan for it on time-sensitive orders. Read more
RUO
Research use only. A labelling and use restriction: not for human or veterinary use, diagnosis, treatment or cosmetic application. Read more
Research use only. Definitions describe laboratory and commercial practice; they are not medical or regulatory advice.

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